Tag: M.W=50-100

Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents. HPLC of Formula: 1739-84-0.

Koshy, David M.;Akhade, Sneha A.;Shugar, Adam;Abiose, Kabir;Shi, Jingwei;Liang, Siwei;Oakdale, James S.;Weitzner, Stephen E.;Varley, Joel B.;Duoss, Eric B.;Baker, Sarah E.;Hahn, Christopher;Bao, Zhenan;Jaramillo, Thomas F. research published 《 Chemical Modifications of Ag Catalyst Surfaces with Imidazolium Ionomers Modulate H₂ Evolution Rates during Electrochemical CO₂ Reduction》, the research content is summarized as follows. Bridging polymer design with catalyst surface science is a promising direction for tuning and optimizing electrochem. reactors that could impact long-term goals in energy and sustainability. Particularly, the interaction between inorganic catalyst surfaces and organic-based ionomers provides an avenue to both steer reaction selectivity and promote activity. Here, we studied the role of imidazolium-based ionomers for electrocatalytic CO₂ reduction to CO (CO₂R) on Ag surfaces and found that they produce no effect on CO₂R activity yet strongly promote the competing hydrogen evolution reaction (HER). By examining the dependence of HER and CO₂R rates on concentrations of CO₂ and HCO₃^–, we developed a kinetic model that attributes HER promotion to intrinsic promotion of HCO₃^– reduction by imidazolium ionomers. We also show that varying the ionomer structure by changing substituents on the imidazolium ring modulates the HER promotion. This ionomer-structure dependence was analyzed via Taft steric parameters and d. functional theory calculations, which suggest that steric bulk from functionalities on the imidazolium ring reduces access of the ionomer to both HCO₃^– and the Ag surface, thus limiting the promotional effect. Our results help develop design rules for ionomer-catalyst interactions in CO₂R and motivate further work into precisely uncovering the interplay between primary and secondary coordination in determining electrocatalytic behavior.

HPLC of Formula: 1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., 1739-84-0.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents. Recommanded Product: 1,2-Dimethyl-1H-imidazole.

Krasovskiy, V. G.;Kapustin, G. I.;Gorbatsevich, O. B.;Glukhov, L. M.;Chernikova, E. A.;Koroteev, A. A.;Kustov, L. M. research published 《 Dicationic disiloxane ionic liquids as heat transfer agents in vacuo》, the research content is summarized as follows. Abstract: Bis(trifluoromethylsulfonyl)imidic dicationic liquids containing a disiloxane linker between the imidazole cations have been synthesized. Their thermal stability was estimated, and their m.ps., viscosity, and volatility in vacuo were measured. The opportunity to use these ionic liquids as heat transfer agents in a dynamic vacuum has been shown.

Recommanded Product: 1,2-Dimethyl-1H-imidazole, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., 1739-84-0.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole is a five-membered heterocyclic moiety that possesses three carbon, two nitrogen, four hydrogen atoms, and two double bonds. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. It is also known as 1, 3-diazole. It contains two nitrogen atoms, in which one nitrogen bear a hydrogen atom, and the other is called pyrrole type nitrogen. Product Details of C5H8N2.

Jin, Chongyue;Wang, Min;Li, Zhilin;Kang, Jin;Zhao, Yan;Han, Jin;Wu, Zengmin research published 《 Two dimensional Co₃O₄/g-C₃N₄ Z-scheme heterojunction: mechanism insight into enhanced peroxymonosulfate-mediated visible light photocatalytic performance》, the research content is summarized as follows. In this study, to improve peroxymonosulfate (PMS)-mediated visible-light photocatalytic performance of g-C₃N₄ in antibiotics degradation and elucidate its mechanism, an ultrathin Co₃O₄ nanomeshes/g-C₃N₄ nanosheets 2D Z-scheme heterojunction composite (x% Co₃O₄/g-C₃N₄) was successfully prepared calcining the mixtures of MOF-Co ultrathin nanosheets and g-C₃N₄. This unique nanomeshes/nanosheets structure with large SSA (153.92 m²/g) possessed an abundance of accessible active sites and large area intimate interfaces between Co₃O₄ and g-C₃N₄, thus remarkably promoting the separation and transport of charge carriers. The as-prepared optimal 10% Co₃O₄/g-C₃N₄ composites exhibited excellent degradation efficiency toward tetracycline (TC) under visible light irradiation and were further enhanced with the addition of PMS. The mechanism of the enhanced TC degradation in Co₃O₄/g-C₃N₄/Vis/PMS system was investigated in detail based on the characterization of the catalysts, TC degradation efficiency assessment, ESR measurements, and reactive oxygen species (ROSs) quenching results. The TC degradation pathway was proposed based on the intermediates identified by the gas chromatog.-mass spectrometer (GC-MS) measurements. This study provides a facile and promising path for the remediation of contaminated water via PMS mediated photocatalysis over highly active g-C₃N₄-based catalysts.

Product Details of C5H8N2, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., 1739-84-0.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole derivatives generally have good solubility in protic solvents. Simple imidazole derivatives, such as 1H-imidazole, 2-methyl-1H-imidazole, and 1,2-dimethylimidazole, have very high solubility in water. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. Their solubility in alcohol is lower than that in water and decreases with increasing molecular weight of the alcohols . Related Products of 1739-84-0.

Jin, Saimeng;Byrne, Fergal P.;Clark, James H.;McElroy, Con Robert;Quinn, Alex;Sherwood, James;Hunt, Andrew J. research published 《 3-Methoxybutan-2-one as a sustainable bio-based alternative to chlorinated solvents》, the research content is summarized as follows. Methylation of acetoin with di-Me carbonate was performed in a sustainable one-step process, with improved process mass intensity (PMI) and atom economy compared to previously published methods. The resulting product, 3-methoxybutan-2-one (MO) was successfully evaluated as a bio-based solvent, while both Kamlet-Taft solvatochromic parameters and Hansen solubility parameters demonstrate its potential viability in the substitution of chlorinated solvents. MO exhibited a low peroxide forming potential and a neg. Ames mutagenicity test and was successfully used as a solvent in a Friedel-Crafts acylation (79% yield compared to 77% in dichloromethane) and for N-alkylations. MO is a renewable oxygenated solvent, with the potential ability to substitute carcinogenic halogenated solvents in some applications.

1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., Related Products of 1739-84-0

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . 10111-08-7, formula is C4H4N2O, Name is 1H-Imidazole-2-carbaldehyde. In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with an increase of the alkyl chain length of the alcohols. Safety of 1H-Imidazole-2-carbaldehyde.

Joel, C.;Jim Livingston, D.;Biju Bennie, R.;Jeyanthi, D.;Vijay Solomon, Rajadurai research published 《 Designing bifunctional phenanthroimidazole chromophores for highly selective ratiometric chemosensing of Cu²⁺/F^– and Co²⁺/F^– ions in organic solvents》, the research content is summarized as follows. Two new phenanthroimidazole based highly sensitive and selective bifunctional probes 2-(1H-imidazol-2-yl)-1H-phenanthro[9,10-d]imidazole (PQIM) and 2-(1H-indol-3-yl)-1H-phenanthro[9,10-d]imidazole (PQIN) have been synthesized which could act as ratiometric sensors. Upon addition of analytes, the receptors exhibited pronounced fluoroionophoric behavior on account of internal charge transfer mechanism (ICT). The mol. sensing studies of both the ligands were explored using UV-visible and fluorescence spectroscopic techniques. It has been observed that the receptor PQIM shows better recognition behavior towards Cu2+/F- while the ligand PQIN exhibited enhanced sensing activity towards Co2+/F-. The binding stoichiometry of the receptor and cation/anion complex was probed to be 1:1 from Job’s plot which were further confirmed from ESI mass spectral techniques and ¹H NMR titrations Further, the binding interactions between these ions (Co²⁺, Cu²⁺ and F^–) with their resp. receptors are probed by d. functional theory calculations This study extends our knowledge on designing chem. compounds that could act as chemosensors in selective binding of certain anions/cations and their sensing mechanisms.

Safety of 1H-Imidazole-2-carbaldehyde, 1H-Imidazole-2-carbaldehyde, also known as 1H-Imidazole-2-carbaldehyde, is a useful research compound. Its molecular formula is C4H4N2O and its molecular weight is 96.09 g/mol. The purity is usually 95%.
1H-Imidazole-2-carboxaldehyde is a novel PTP1b inhibitor with potential application to treat type 2 diabetes.
1H-Imidazole-2-carboxaldehyde is a broad-spectrum antimicrobial that has been shown to inhibit the growth of bacteria by interfering with protein synthesis. It binds to the cytosolic protein and receptor molecule, which are involved in the activation of bacterial enzymes. Imidazole-2-carboxaldehyde reacts with anhydrous sodium and copper complex to produce hydrogen bonds, which prevent the formation of the nitrogen atoms necessary for cellular processes. This chemical also has biological properties such as glyoxal, which inhibits bacterial growth by reacting with amino groups on proteins., 10111-08-7.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole derivatives generally have good solubility in protic solvents. Simple imidazole derivatives, such as 1H-imidazole, 2-methyl-1H-imidazole, and 1,2-dimethylimidazole, have very high solubility in water. 10111-08-7, formula is C4H4N2O, Name is 1H-Imidazole-2-carbaldehyde. Their solubility in alcohol is lower than that in water and decreases with increasing molecular weight of the alcohols . Application In Synthesis of 10111-08-7.

Hu, Ming-Hao;Yu, Bing-Ying;Wang, Xiaodong;Jin, Guangyi research published 《 Drug-like biimidazole derivatives dually target c-MYC/BCL-2 G-quadruplexes and inhibit acute myeloid leukemia》, the research content is summarized as follows. Chemotherapy is the main approach for treating acute myeloid leukemia (AML). However, this therapy can cause severe side effects as well as drug resistance, hence calling for new therapeutic strategies. As c-MYC and BCL-2 are often overexpressed in AML, and synergism between c-MYC and BCL-2 promotes tumorigenesis, therefore, dual targeting of c-MYC/BCL-2 promoter G-quadruplexes (G4s) and then inhibiting the targeted gene expression would be a potential strategy in ALM treatment. In this work, in the search of dual ligands, we performed a screening assay with an inhouse, imidazole-based compound library. Consequently, two drug-like biimidazole derivatives were identified as selective c-MYC/BCL-2 G4 binders, of which, BIM-2 was selected as the candidate for inhibiting AML cell growth. Then, BIM-2 was demonstrated to downregulate both c-MYC and BCL-2 expression, and thereby cause cell cycle arrest at G0/G1 phase and apoptosis in AML cells. Furthermore, the possible end-stacking binding modes between BIM-2 and c-MYC/BCL-2 G4s were revealed by NMR and mol. docking studies. Accordingly, this study provides a new class of drug-like dual-selective c-MYC/BCL-2 G4 ligands for the potential treatment of AML.

10111-08-7, 1H-Imidazole-2-carbaldehyde, also known as 1H-Imidazole-2-carbaldehyde, is a useful research compound. Its molecular formula is C4H4N2O and its molecular weight is 96.09 g/mol. The purity is usually 95%.
1H-Imidazole-2-carboxaldehyde is a novel PTP1b inhibitor with potential application to treat type 2 diabetes.
1H-Imidazole-2-carboxaldehyde is a broad-spectrum antimicrobial that has been shown to inhibit the growth of bacteria by interfering with protein synthesis. It binds to the cytosolic protein and receptor molecule, which are involved in the activation of bacterial enzymes. Imidazole-2-carboxaldehyde reacts with anhydrous sodium and copper complex to produce hydrogen bonds, which prevent the formation of the nitrogen atoms necessary for cellular processes. This chemical also has biological properties such as glyoxal, which inhibits bacterial growth by reacting with amino groups on proteins., Application In Synthesis of 10111-08-7

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole is a five-membered heterocyclic moiety that possesses three carbon, two nitrogen, four hydrogen atoms, and two double bonds. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. It is also known as 1, 3-diazole. It contains two nitrogen atoms, in which one nitrogen bear a hydrogen atom, and the other is called pyrrole type nitrogen. Computed Properties of 1739-84-0.

Hu, Xiao;Zhang, Runan;Wemyss, Alan M.;Elbanna, Mohamed A.;Heeley, Ellen L.;Arafa, Mustafa;Bowen, Chris;Wang, Shifeng;Geng, Xueyu;Wan, Chaoying research published 《 Tuning triboelectric and energy harvesting properties of dielectric elastomers via dynamic ionic crosslinks》, the research content is summarized as follows. The bromination of poly(isobutylene-co-isoprene) rubber introduces a small amount of bromide groups (1-2 mol%) to the elastomer backbone and creates new opportunities for functionalisation, as compared to other saturated and diene elastomers. In this work, three types of nucleophile reagents: namely pyridine, triphenylphosphine and imidazoles bearing four types of side groups of Me, Et, hydroxyl or vinyl group were introduced to brominated poly(isobutylene-co-isoprene) rubber (BIIR) through nucleophile substitution with the bromine via solid-state rubber compounding and curing processes. The resulted ionic aggregates act as phys. crosslinks and their size and d. directly affected the mech. reinforcement, self-healing and dynamic mech. properties of the elastomers. The smaller and polar imidazolyl/bromine pairs led to the highest reinforcement beyond even the sulfur-cured BIIR counterparts. The 1-Et imidazole (EIm) modified BIIR showed the highest tensile strength of 17.01 ± 1.89 MPa and elongation at break of 1402 ± 69% with self-healing efficiency of 63.7%, after being treated at 140°C for 30 min. In addition, the inclusion of the ionic clusters enhanced the relative permittivity of the elastomer, thereby enhancing the energy conversion efficiencies. The nucleophile substitution reaction via conventional solid-state rubber compounding processes provides a facile crosslinking and reinforcement strategy for halogen-containing polymers. In addition, the dynamic ionic crosslinking networks spontaneously benefit electromech. and self-healing properties of the dielec. elastomers.

1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., Computed Properties of 1739-84-0

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole based anticancer drug find applications in cancer chemotherapy. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC). Recommanded Product: 1,2-Dimethyl-1H-imidazole.

Hua, Derun;Ding, Hao;Liu, Yunfeng;Li, Jian;Han, Baojun research published 《 Dehydration of Xylose to Furfural over Imidazolium-Based Ionic Liquid with Phase Separation》, the research content is summarized as follows. An environmentally friendly catalyst and task-specific ionic liquid (IL), 1-(4-sulfonic acid) butyl-3-cetyl-2-Me imidazolium hydrogen sulfate, was applied to the dehydration of xylose to furfural. Its structure was determined by FT-IR, ¹H NMR technologies. The solubility of IL in water changed with the temperature, and had the advantages of homogeneous and heterogeneous catalysts. At the given conditions, xylose conversion of 95.3% and furfural yield of 67.5% were achieved over IL.

Recommanded Product: 1,2-Dimethyl-1H-imidazole, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., 1739-84-0.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents. SDS of cas: 1739-84-0.

Huang, Lingyun;Yang, Yinxin;Niu, Zhen;Wu, Ruiyao;Fan, Weifeng;Dai, Quanquan;He, Jianyun;Bai, Chenxi research published 《 Catalyst-Free Vitrimer Cross-Linked by Biomass-Derived Compounds with Mechanical Robustness, Reprocessability, and Multishape Memory Effects》, the research content is summarized as follows. Vitrimerization of thermoset polymers plays an important role in addressing resource recovery and reuse. Vitrimer elastomers with good mech. properties often require well-designed crosslinking agents or fillers, but this increases processing complexity or reduces vitrimer dynamic properties. In this report, a simple green strategy to build a strong vitrimer elastomer is designed. Com. available epoxidized natural rubber (ENR) is crosslinked with biomass-derived D-Fructose 1,6-bisphosphoric acid to get a vitrimer elastomer crosslinked by β-hydroxy phosphate ester bonds and has abundant hydrogen bonds. Hydrogen bonds can preferentially break and dissipate energy under external forces, which makes the sample robust. The topol. network can be reformed at high temperatures through the dynamic exchange of β-hydroxy phosphate ester bonds, which gives the material malleability and recyclability. In addition, through the strategy of combining reprocessing and welding, multiple shape memory effects can be achieved in one postprocessing step. Considering that a variety of com. available epoxy polymers are easily available, it is believed that this strategy can be a simple and versatile way to enable com. epoxy polymers to achieve green crosslinking through biomass crosslink agents, which results in robust and recyclable vitrimers based on β-hydroxy phosphate bonds.

1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., SDS of cas: 1739-84-0

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole Biochem/physiol Actions: Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. It also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes. Related Products of 1739-84-0.

Huang, Lingyun;Yang, Yinxin;Wu, Ruiyao;Fan, Weifeng;Dai, Quanquan;He, Jianyun;Bai, Chenxi research published 《 Boron nitride and hyperbranched polyamide assembled recyclable polyisoprene vitrimer with robust mechanical properties, high thermal conductivity and remoldability》, the research content is summarized as follows. Rubber has huge potential applications for thermal management due to its outstanding softness and elasticity, however, its low thermal conductivity limits its applications, and the vulcanized rubber also has the problem of being unrecoverable. Therefore, the development of recyclable rubber-based material with good mech. properties, high thermal conductivity remains a challenge. Herein, the dynamic β-hydroxyl ester bonds were introduced into the composites of the epoxidized boron nitride (EBN) and the epoxidized polyisoprene (EPI) matrix via carboxyl-terminated hyperbranched polyamide (HBPA), forming dynamic covalently crosslinking rubber-based vitrimers. The covalent-bonds-mediated interface reduces the phonon scattering and enables the material to have a relatively high thermal conductivity of 0.51 W/mK under a loading of 50 phr (parts per one hundred parts of rubber) of EBN. In addition, the introduction of exchangeable bonds brings the materials the capability to change the network topol. at high temperatures, exhibiting excellent recyclability and remoldability.

1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., Related Products of 1739-84-0

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem