Zhao, Xiaohui et al. published their research in Journal of Dispersion Science and Technology in 2017 | CAS: 21252-69-7

1-Octyl-1H-imidazole (cas: 21252-69-7) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. Imidazole is incorporated into many important biological compounds. The most pervasive is the amino acid histidine, which has an imidazole side-chain. Histidine is present in many proteins and enzymes, e.g. by binding metal cofactors, as seen in hemoglobin.HPLC of Formula: 21252-69-7

Adsorption and thermodynamic properties of dissymmetric gemini imidazolium surfactants with different spacer length was written by Zhao, Xiaohui;An, Dong;Ye, Zhiwen. And the article was included in Journal of Dispersion Science and Technology in 2017.HPLC of Formula: 21252-69-7 This article mentions the following:

A series of dissym. gemini imidazolium surfactants with different spacer length ([CmCsCni.m.]Br2, m + n = 24, m = 12, 14, 16, 18; s = 2, 4, 6) were synthesized and characterized by 1H NMR and ESI-MS spectroscopy. Their adsorption and thermodn. properties were investigated by the surface tension and elec. conductivity methods. Consequently, the surface activity parameters (cmc, γcmc, πcmc, pC20, cmc/C20, Γmax, Amin) and thermodn. parameters (Δ;Gmθ, ΔHmθ, ΔSmθ) were obtained. The effects of the dissymmetry (m/n) and the spacer length (s) on the surface activity and micellization process of surfactants have been discussed in detail. In the experiment, the researchers used many compounds, for example, 1-Octyl-1H-imidazole (cas: 21252-69-7HPLC of Formula: 21252-69-7).

1-Octyl-1H-imidazole (cas: 21252-69-7) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. Imidazole is incorporated into many important biological compounds. The most pervasive is the amino acid histidine, which has an imidazole side-chain. Histidine is present in many proteins and enzymes, e.g. by binding metal cofactors, as seen in hemoglobin.HPLC of Formula: 21252-69-7

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Zhou, Kai et al. published their research in Organic & Biomolecular Chemistry in 2020 | CAS: 1632-83-3

1-Methylbenzimidazole (cas: 1632-83-3) belongs to imidazole derivatives. Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. Imidazole has been usedin the lysis, wash and elution buffer for the purification of histidine tagged Sonic Hedgehog(shh-N) protein, in elution buffer in stepwise gradient for the purification of histidine tagged aldo keto reductases using nickel affinity chromatography, as a component of homogenization buffer for the purification of phagosomal compartments from dendritic cells.COA of Formula: C8H8N2

Iron-catalyzed [3+2]-cycloaddition of in situ generated N-ylides with alkynes or olefins: access to multi-substituted/polycyclic pyrrole derivatives was written by Zhou, Kai;Bao, Ming;Huang, Jingjing;Kang, Zhenghui;Xu, Xinfang;Hu, Wenhao;Qian, Yu. And the article was included in Organic & Biomolecular Chemistry in 2020.COA of Formula: C8H8N2 This article mentions the following:

An iron-catalyzed one-pot three-component reaction of 1-substituted benzimidazoles with diazoacetates and electron-deficient alkynes or alkenes has been reported. Mechanistically, the reaction goes through a 1,3-dipolar cycloaddition of catalytically generated benzimidazolium N-ylides with various activated alkynes or alkenes, leading to multi-substituted and polycyclic fused pyrrole derivatives, resp. In the experiment, the researchers used many compounds, for example, 1-Methylbenzimidazole (cas: 1632-83-3COA of Formula: C8H8N2).

1-Methylbenzimidazole (cas: 1632-83-3) belongs to imidazole derivatives. Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. Imidazole has been usedin the lysis, wash and elution buffer for the purification of histidine tagged Sonic Hedgehog(shh-N) protein, in elution buffer in stepwise gradient for the purification of histidine tagged aldo keto reductases using nickel affinity chromatography, as a component of homogenization buffer for the purification of phagosomal compartments from dendritic cells.COA of Formula: C8H8N2

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Faundez, Claudio A. et al. published their research in Fluid Phase Equilibria in 2013 | CAS: 35487-17-3

1-Methyl-1H-imidazol-3-ium chloride (cas: 35487-17-3) belongs to imidazole derivatives. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. Imidazole has been usedin the lysis, wash and elution buffer for the purification of histidine tagged Sonic Hedgehog(shh-N) protein, in elution buffer in stepwise gradient for the purification of histidine tagged aldo keto reductases using nickel affinity chromatography, as a component of homogenization buffer for the purification of phagosomal compartments from dendritic cells.Safety of 1-Methyl-1H-imidazol-3-ium chloride

Consistency test of solubility data of ammonia in ionic liquids using the modified Peng-Robinson equation of Kwak and Mansoori was written by Faundez, Claudio A.;Diaz-Valdes, Joaquin F.;Valderrama, Jose O.. And the article was included in Fluid Phase Equilibria in 2013.Safety of 1-Methyl-1H-imidazol-3-ium chloride This article mentions the following:

Phase equilibrium data of temperature, pressure and solubility (T-P-x) of ammonia in different types of ionic liquids over wide ranges of temperatures and pressures are modeled and tested for thermodn. consistency. The modified Peng-Robinson equation of state proposed by Kwak and Mansoori is used for correlating the isothermal PX data and a flexible thermodn. consistency method applied to analyze forty seven isothermal P-x data available in the open literature. Modeling is found acceptable in all cases, meaning that deviations in correlating the data are low, proving at the same time the claimed flexibility of a well-founded model that uses simple van der Waals mixing rules. For all cases, the thermodn. consistency method gives a clear conclusion about consistency or inconsistency of a set of exptl. T-P-x data based on the established criteria. In the experiment, the researchers used many compounds, for example, 1-Methyl-1H-imidazol-3-ium chloride (cas: 35487-17-3Safety of 1-Methyl-1H-imidazol-3-ium chloride).

1-Methyl-1H-imidazol-3-ium chloride (cas: 35487-17-3) belongs to imidazole derivatives. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. Imidazole has been usedin the lysis, wash and elution buffer for the purification of histidine tagged Sonic Hedgehog(shh-N) protein, in elution buffer in stepwise gradient for the purification of histidine tagged aldo keto reductases using nickel affinity chromatography, as a component of homogenization buffer for the purification of phagosomal compartments from dendritic cells.Safety of 1-Methyl-1H-imidazol-3-ium chloride

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Pawar, Arvind et al. published their research in Research on Chemical Intermediates in 2021 | CAS: 1632-83-3

1-Methylbenzimidazole (cas: 1632-83-3) belongs to imidazole derivatives. 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. The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents.n increase of the alkyl chain length of the alcohols. Safety of 1-Methylbenzimidazole

One-pot multicomponent synthesis of N-sulfonyl amidines using magnetic separable nanoparticles-decorated N-heterocyclic carbene complex with copper was written by Pawar, Arvind;Gajare, Shivanand;Patil, Audumbar;Kurane, Rajanikant;Rashinkar, Gajanan;Patil, Suresh. And the article was included in Research on Chemical Intermediates in 2021.Safety of 1-Methylbenzimidazole This article mentions the following:

Magnetic separable nanoparticles-decorated N-heterocyclic carbene complex with copper (MNP[1-Me benzimidazole]NHC@Cu) has been prepared by covalent grafting of ionic liquid like 1-Me benzimidazole unit on the surface of chlorofunctionalized Fe3O4 magnetic nanoparticles (MNPs) followed by metalation with copper(I) iodide. MNP[1-Me benzimidazole]NHC@Cu complex has been characterized by different techniques including Fourier transform IR spectroscopy, thermogravimetric anal., energy-dispersive X-ray anal., X-ray diffraction, transmission electron microscopy and vibrating sample magnetometer. MNP[1-Me benzimidazole]NHC@Cu complex was successfully implemented as heterogeneous catalyst in one-pot multicomponent synthesis of N-sulfonyl amidines from phenylacetylene, tosyl azide and amines at room temperature Complex could be recycled six times without significant loss in the yield of product. In the experiment, the researchers used many compounds, for example, 1-Methylbenzimidazole (cas: 1632-83-3Safety of 1-Methylbenzimidazole).

1-Methylbenzimidazole (cas: 1632-83-3) belongs to imidazole derivatives. 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. The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents.n increase of the alkyl chain length of the alcohols. Safety of 1-Methylbenzimidazole

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Staab, Heinz A. et al. published their research in Justus Liebigs Annalen der Chemie in 1966 | CAS: 3034-41-1

1-Methyl-4-nitroimidazole (cas: 3034-41-1) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. Imidazole has been usedin the lysis, wash and elution buffer for the purification of histidine tagged Sonic Hedgehog(shh-N) protein, in elution buffer in stepwise gradient for the purification of histidine tagged aldo keto reductases using nickel affinity chromatography, as a component of homogenization buffer for the purification of phagosomal compartments from dendritic cells.Quality Control of 1-Methyl-4-nitroimidazole

Proton resonance studies on aromatic heterocycles. III. Hydrogen-deuterium exchange with azoles and azolium salts was written by Staab, Heinz A.;Irngartinger, Hermann;Mannschreck, Albrecht;Wu, Mou-Thai. And the article was included in Justus Liebigs Annalen der Chemie in 1966.Quality Control of 1-Methyl-4-nitroimidazole This article mentions the following:

For several azoles and azolium salts were measured the N.M.R. spectra and assignments made; with their aid the H-D exchange of the ring H atoms was investigated. The dependence of the relative deuteration rates on structural factors was discussed in connection with biochem. questions. The N.M.R. spectra of various oxazoles and oxazolium salts were also measured, and also investigated by H-D exchange. 4-Nitroimidazole (I) in D2O (1% solution) heated 13.5 hrs. at 100° resulted in deuteration at C-2 and C-4 (or 5) in the ratio 5:3. A similar experiment in a citrate buffered solution (pH 5.1) gave the same relative deuteration. After heating I in 0.8M NaOD in D2O 12 hrs., both H-2 and H-4 (or 5) were completely exchanged. In contrast, 1-methyl-4-nitroimidazole in D2O (12.5 hrs., 100°, 2.5% solution) was more strongly deuterated at C-5 than at C-2; 90% for H-5 and 50% for H-2. Surprisingly, 1-methyl-5-nitroimidazole under the sample conditions underwent complete exchange at H-2 and only 10% at H-4. The half-life times for deuteration of 4,5-dipropyloxazole and 4,5-diphenyloxazole in MeOD were 600 min. (60°) and 1100 min. (69°), while the 2-position of the corresponding methiodides was completely deuterated in MeOD at 37° after 3 min., In the experiment, the researchers used many compounds, for example, 1-Methyl-4-nitroimidazole (cas: 3034-41-1Quality Control of 1-Methyl-4-nitroimidazole).

1-Methyl-4-nitroimidazole (cas: 3034-41-1) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. Imidazole has been usedin the lysis, wash and elution buffer for the purification of histidine tagged Sonic Hedgehog(shh-N) protein, in elution buffer in stepwise gradient for the purification of histidine tagged aldo keto reductases using nickel affinity chromatography, as a component of homogenization buffer for the purification of phagosomal compartments from dendritic cells.Quality Control of 1-Methyl-4-nitroimidazole

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Yutilov, Yu. M. et al. published their research in Khimiya Geterotsiklicheskikh Soedinenii in 1989 | CAS: 52538-09-7

2,3-Dimethyl-3H-imidazo[4,5-c]pyridine (cas: 52538-09-7) belongs to imidazole derivatives. The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with a Imidazole has been usedin the lysis, wash and elution buffer for the purification of histidine tagged Sonic Hedgehog(shh-N) protein, in elution buffer in stepwise gradient for the purification of histidine tagged aldo keto reductases using nickel affinity chromatography, as a component of homogenization buffer for the purification of phagosomal compartments from dendritic cells.HPLC of Formula: 52538-09-7

Synthesis and proton NMR spectra of 2-heteroaryl-substituted imidazo[4,5-b]pyridines and imidazo[4,5-c]pyridines was written by Yutilov, Yu. M.;Shcherbina, L. I.;Efremenko, A. F.. And the article was included in Khimiya Geterotsiklicheskikh Soedinenii in 1989.HPLC of Formula: 52538-09-7 The following contents are mentioned in the article:

The title compounds were prepared by oxidation of mixtures of 2,3- or 3,4-pyridinediamines with heterocycles containing an active Me group in the presence of S. Other methods involved cyclization of pyridinediamines with picoline N-oxides and 2-pyridinethiocarboxanilides and the intramol. oxidative cyclization of N4-(2-pyridylmethyl)-3,4-pyridinediamine. In most cases, the yield was �0%. The NMR spectra of 2-pyridylimidazopyridines were examined This study involved multiple reactions and reactants, such as 2,3-Dimethyl-3H-imidazo[4,5-c]pyridine (cas: 52538-09-7HPLC of Formula: 52538-09-7).

2,3-Dimethyl-3H-imidazo[4,5-c]pyridine (cas: 52538-09-7) belongs to imidazole derivatives. The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with a Imidazole has been usedin the lysis, wash and elution buffer for the purification of histidine tagged Sonic Hedgehog(shh-N) protein, in elution buffer in stepwise gradient for the purification of histidine tagged aldo keto reductases using nickel affinity chromatography, as a component of homogenization buffer for the purification of phagosomal compartments from dendritic cells.HPLC of Formula: 52538-09-7

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Pellizzaro, Maria L. et al. published their research in Organic & Biomolecular Chemistry in 2012 | CAS: 1384100-95-1

4-(tert-Butyl)-1H-imidazol-2-amine hydrochloride (cas: 1384100-95-1) belongs to imidazole derivatives. Imidazole is the basic core of some natural products such as histidine, purine, histamine and DNA based structures, etc. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. Imidazole also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes.Name: 4-(tert-Butyl)-1H-imidazol-2-amine hydrochloride

Design, synthesis and binding studies of a novel quadruple ADDA hydrogen-bond array was written by Pellizzaro, Maria L.;Barrett, Simon A.;Fisher, Julie;Wilson, Andrew J.. And the article was included in Organic & Biomolecular Chemistry in 2012.Name: 4-(tert-Butyl)-1H-imidazol-2-amine hydrochloride The following contents are mentioned in the article:

The design and synthesis of a novel ADDA hydrogen-bond array is described. The ureidodiimidazole motif (I UDIM) engages in interactions with complementary diamidonaphthyridine (II DAN) motifs with an association constant Ka = 825 ± 16 M-1 in chloroform. 1H NMR and mol. modeling studies were carried out in order to explain the unexpected behavior of this new supramol. motif. These revealed that a combination of effects including; an energetic bias for the folded conformer, subtle differences in shape complementarity between the two components and the potential for self-association of I disfavor higher affinity interactions between the two components. This study involved multiple reactions and reactants, such as 4-(tert-Butyl)-1H-imidazol-2-amine hydrochloride (cas: 1384100-95-1Name: 4-(tert-Butyl)-1H-imidazol-2-amine hydrochloride).

4-(tert-Butyl)-1H-imidazol-2-amine hydrochloride (cas: 1384100-95-1) belongs to imidazole derivatives. Imidazole is the basic core of some natural products such as histidine, purine, histamine and DNA based structures, etc. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. Imidazole also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes.Name: 4-(tert-Butyl)-1H-imidazol-2-amine hydrochloride

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Yutilov, Yu. M. et al. published their research in Khimiya Geterotsiklicheskikh Soedinenii in 1975 | CAS: 52538-09-7

2,3-Dimethyl-3H-imidazo[4,5-c]pyridine (cas: 52538-09-7) belongs to imidazole derivatives. The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with a The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents.n increase of the alkyl chain length of the alcohols. Application In Synthesis of 2,3-Dimethyl-3H-imidazo[4,5-c]pyridine

2-Aldehydes of imidazo[4,5-b]- and imidazo[4,5-c]pyridines was written by Yutilov, Yu. M.;Kovaleva, L. I.. And the article was included in Khimiya Geterotsiklicheskikh Soedinenii in 1975.Application In Synthesis of 2,3-Dimethyl-3H-imidazo[4,5-c]pyridine The following contents are mentioned in the article:

Imidazopyridinecarboxaldehydes (I, R = Me, PhCH2, Ph, R1 = CHO), II (R1 = CHO), III (R1 = CHO), and IV (R = PhCH2, Ph, R1 = CHO) were obtained in 50-84% yields by oxidation of the corresponding 2-methyl derivative with SeO2 in dioxane at 70-80°. Condensation of the aldehydes with CH2(CO2H)2 gave 43-60% acrylic acid derivatives I (R = Me, R1 = CH:CHCO2H). II (R1 = CH:CHCO2H), and IV (R = Ph, R1 = CH:CHCO2H). The cyano derivatives I (R = Me, PhCH2R1 = CN), II (R1 = CN), and IV (R = PhCH2, Ph, R1 = CN) were obtained in 65-93% by boiling the corresponding aldoximes with Ac2O 7 hr. Amides I (R = Me, PhCH2, R1 = CONM2), II (R1 = CONH2), and IV (R = Ph, R1 = CONH2) were obtained in 60-82% yields by oxidation of the corresponding nitriles with concentrated H2SO4. This study involved multiple reactions and reactants, such as 2,3-Dimethyl-3H-imidazo[4,5-c]pyridine (cas: 52538-09-7Application In Synthesis of 2,3-Dimethyl-3H-imidazo[4,5-c]pyridine).

2,3-Dimethyl-3H-imidazo[4,5-c]pyridine (cas: 52538-09-7) belongs to imidazole derivatives. The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with a The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents.n increase of the alkyl chain length of the alcohols. Application In Synthesis of 2,3-Dimethyl-3H-imidazo[4,5-c]pyridine

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Coubrough, Heather M. et al. published their research in Chemistry – A European Journal in 2019 | CAS: 1384100-95-1

4-(tert-Butyl)-1H-imidazol-2-amine hydrochloride (cas: 1384100-95-1) belongs to imidazole derivatives. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. Imidazole also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes.Product Details of 1384100-95-1

Supramolecular Self-Sorting Networks using Hydrogen-Bonding Motifs was written by Coubrough, Heather M.;van der Lubbe, Stephanie C. C.;Hetherington, Kristina;Minard, Aisling;Pask, Christopher;Howard, Mark J.;Fonseca Guerra, Celia;Wilson, Andrew J.. And the article was included in Chemistry – A European Journal in 2019.Product Details of 1384100-95-1 The following contents are mentioned in the article:

A current objective in supramol. chem. is to mimic the transitions between complex self-sorted systems that represent a hallmark of regulatory function in nature. In this work, a self-sorting network, comprising linear hydrogen motifs, was created. Selecting six hydrogen-bonding motifs capable of both high-fidelity and promiscuous mol. recognition gave rise to a complex self-sorting system, which included motifs capable of both narcissistic and social self-sorting. Examination of the interactions between individual components, exptl. and computationally, provided a rationale for the product distribution during each phase of a cascade. This reasoning holds through up to five sequential additions of six building blocks, resulting in the construction of a biomimetic network in which the presence or absence of different components provides multiple unique pathways to distinct self-sorted configurations. This study involved multiple reactions and reactants, such as 4-(tert-Butyl)-1H-imidazol-2-amine hydrochloride (cas: 1384100-95-1Product Details of 1384100-95-1).

4-(tert-Butyl)-1H-imidazol-2-amine hydrochloride (cas: 1384100-95-1) belongs to imidazole derivatives. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. Imidazole also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes.Product Details of 1384100-95-1

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Miroshnichenko, N. S. et al. published their research in Ukrainskii Khimicheskii Zhurnal (Russian Edition) in 1974 | CAS: 52538-09-7

2,3-Dimethyl-3H-imidazo[4,5-c]pyridine (cas: 52538-09-7) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. Imidazole based anticancer drug find applications in cancer chemotherapy. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC).Related Products of 52538-09-7

Determination of the structure of 2-methylimidazo[4,5-c]pyridine glycosides was written by Miroshnichenko, N. S.;Kovalenko, A. S.;Stetsenko, A. V.. And the article was included in Ukrainskii Khimicheskii Zhurnal (Russian Edition) in 1974.Related Products of 52538-09-7 The following contents are mentioned in the article:

Imidazopyridine glycosides (I; R = tri-O-acetyl-β-D-ribopyranosyl, β-D-ribopyranosyl, tri-O-acetyl-β-D-xylopyranosyl β-D-xylopyranosyl, tetra-O-acetyl-β-D-galactopyranosyl, β-D-galactopyranosyl) were prepared by known methods in 49-86%yields and their structures confirmed by NMR. This study involved multiple reactions and reactants, such as 2,3-Dimethyl-3H-imidazo[4,5-c]pyridine (cas: 52538-09-7Related Products of 52538-09-7).

2,3-Dimethyl-3H-imidazo[4,5-c]pyridine (cas: 52538-09-7) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. Imidazole based anticancer drug find applications in cancer chemotherapy. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC).Related Products of 52538-09-7

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem