Category: 478935-29-4

Acid-induced chemoselective arylthiolations of electron-rich arenes in ionic liquids from sodium arylsulfinates: the reducibility of halide anions in [Hmim]Br was written by Xu, Zhu-bing;Lu, Guo-ping;Cai, Chun. And the article was included in Organic & Biomolecular Chemistry in 2017.Related Products of 478935-29-4 The following contents are mentioned in the article:

An acid-induced protocol for the chemoselective arylthiolations of electron-rich arenes in ionic liquids from sodium arylsulfinates is introduced. The chem., in which [Hmim]Br (heaxylmethylimidazolium bromide) is used as both a solvent and a reducer, provides several advantages including odorless and simple operation, inexpensive reagents, recyclable solvents and gram-scale synthesis. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Related Products of 478935-29-4).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. Imidazole has become an important synthon in the development of new drugs. 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 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Ring-opening of N-tosyl aziridines with hydroxyl compounds catalyzed by acidic ionic liquid was written by Li, Yuling;Gu, Dagong;Xu, Xiaoping;Ji, Shunjun. And the article was included in Chinese Journal of Chemistry in 2009.Related Products of 478935-29-4 The following contents are mentioned in the article:

The ring-opening of two types of N-tosyl aziridines with hydroxyl compounds was studied. The aziridines reacted smoothly with alcs. in the presence of functional ionic liquid [hmim]HSO₄ to afford the corresponding β-amino ethers in moderate to good yields with high regioselectivity. The recyclable property of [hmim]HSO₄ was demonstrated in the process. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Related Products of 478935-29-4).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. Imidazole has become an important synthon in the development of new drugs. 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.Related Products of 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Study on the alkylation of isobutane/butene in acidic ionic liquids was written by Liu, Ying;Hu, Rui-sheng;Liu, Gui-li;Xu, Chun-ming. And the article was included in Fenzi Cuihua in 2010.SDS of cas: 478935-29-4 The following contents are mentioned in the article:

The catalytic performance of acidic ionic liquids on the isobutane/butene alkylation was investigated. The acidic strength of ionic liquids has been improved by modified cation, anion and liquid acid. The amount of TMP in the [MBSIM]OTf alkylate can reach 69.8%. The reaction system can be used for 8 times without significant decrease in catalytic performance. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4SDS of cas: 478935-29-4).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) 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).SDS of cas: 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Novel ionic liquid-mediated approach for the synthesis of tetracyclic[6,5,5,5]indole ring was written by Srivastava, Arjita;Siddiqui, Ibadur Rahman. And the article was included in Journal of Heterocyclic Chemistry in 2020.Formula: C10H20N2O4S The following contents are mentioned in the article:

A novel acidic ionic liquid-catalyzed protocol for the synthesis of diversely substituted tetracyclic indole core was devised. The application of ionic liquid provided this methodol. with various merits over conventional methods regarding reaction time, yield and ease of handling. Acidic ionic liquid was employed as a catalytic agent in this protocol. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Formula: C10H20N2O4S).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) 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 also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes.Formula: C10H20N2O4S

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

One-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones catalyzed by acidic ionic liquid was written by Ma, Jing-Jun;Zang, Xiao-Huan;Zhou, Xin;Wang, Chun;Li, Jing-Ci;Li, Qing. And the article was included in Indian Journal of Chemistry in 2007.Quality Control of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate The following contents are mentioned in the article:

3,4-Dihydropyrimidin-2(1H)-ones were synthesized via one-pot reaction of aromatic aldehydes, Et acetoacetate and urea or thiourea catalyzed by room temperature ionic liquid [hmim]HSO₄. It was observed that the proposed method is fast, efficient and environmentally benign. The reaction time is 15 ∼ 55 min with the yields between 82 ∼ 97 %. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Quality Control of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) 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. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.Quality Control of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Acidic ionic liquid-catalyzed highly efficient reaction of indoles to α,β-unsaturated ketones was written by Gu, Da-gong;Ji, Shun-jun;Wang, Hong-xia;Xu, Qiu-yan. And the article was included in Synthetic Communications in 2008.Recommanded Product: 478935-29-4 The following contents are mentioned in the article:

A novel method for the Michael reaction of indoles to α,β-unsaturated ketones catalyzed by acidic ionic liquid was reported. The authors obtained the corresponding products in excellent yields in the presence of [hmim]HSO₄. Development of this method resulted in a new protocol for the synthesis of β-indolylketones. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Recommanded Product: 478935-29-4).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) 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. 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. Recommanded Product: 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Chitosan/ionic liquid forms a renewable and reusable catalyst system used for the synthesis of highly functionalized spiro derivatives was written by Rai, Pratibha;Srivastava, Madhulika;Singh, Jaya;Singh, Jagdamba. And the article was included in New Journal of Chemistry in 2014.HPLC of Formula: 478935-29-4 The following contents are mentioned in the article:

Chitosan, a reusable heterogeneous catalyst, can be combined with an ionic liquid as a green solvent to generate a highly efficient catalyst system for densely functionalized and diversified target mol. The reaction is completed with a good to excellent yield. This procedure demonstrates an eco-friendly catalyst system and eliminates the use of toxic transition metal catalysts, bases and volatile organic solvents, which adversely affect the environment and human beings. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4HPLC of Formula: 478935-29-4).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) 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.HPLC of Formula: 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Selective and efficient oxidation of sulfides to sulfoxides using ceric ammonium nitrate (CAN)/Bronsted acidic ionic liquid was written by Hajipour, Abdol R.;Khazdooz, Leila;Ruoho, Arnold E.. And the article was included in Phosphorus, Sulfur and Silicon and the Related Elements in 2009.COA of Formula: C10H20N2O4S The following contents are mentioned in the article:

A selective and efficient procedure for the oxidation of sulfides to the corresponding sulfoxides was reported using ceric ammonium nitrate in the presence of methylimidazolium hydrogen sulfate as Bronsted acidic ionic liquid ([Hmim]HSO₄) as the solvent under mild conditions. The use of nontoxic and inexpensive materials, straightforward procedure, short reaction times, and good yields of the products are the major advantages of this method. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4COA of Formula: C10H20N2O4S).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) 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 derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division.COA of Formula: C10H20N2O4S

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Synthesis of N-(α-Alkoxyalkyl)benzotriazoles catalyzed by acidic ionic liquid at room temperature was written by Wang, Hong-Xia;Ji, Shun-Jun;Gu, Da-Gong. And the article was included in Chinese Journal of Chemistry in 2007.Recommanded Product: 478935-29-4 The following contents are mentioned in the article:

N-(α-Alkoxyalkyl)benzotriazoles were synthesized with ≤99% yield via the condensation of benzotriazole with various aldehydes and alcs. catalyzed by acidic ionic liquid [hmim]HSO₄ (hmim = 1-hexyl-3-methylimidazolium) at room temperature This novel method was effective when (EtO)₃CH was utilized instead of alcs. Moreover, acidic ionic liquid could be reused easily with no significant degradation of its catalytic activity. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Recommanded Product: 478935-29-4).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) 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. 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).Recommanded Product: 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Improvement the activity and selectivity of Fenton system in the oxidation of alcohols was written by Yang, Guoqiang;Lin, Qiuxing;Hu, Xingbang;Wu, Youting;Zhang, Zhibing. And the article was included in Journal of Catalysts in 2014.Computed Properties of C10H20N2O4S The following contents are mentioned in the article:

The reactivity and selectivity of Fenton system (Fe2+/H2O2) were improved with N-hydroxyphthalimide (NHPI) as cocatalyst.The oxidation process of benzyl alc. to benzaldehyde has been studied. The reaction catalyzed by this new Fe2+/H2O2/NHPI system can be well performed under room temperature without adding any organic solvent. Besides, this catalyst system is effective for the oxidation of different alcs. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Computed Properties of C10H20N2O4S).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) 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 derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division.Computed Properties of C10H20N2O4S

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem