Category: 478935-29-4

Synthesis and evaluation of anticancer activity of some new 3-aminoalkylated indole derivatives was written by Jadhvar, Suresh C.;Kasraliker, Hanmant M.;Bhusare, Sudhakar R.. And the article was included in American Journal of PharmTech Research in 2015.Application of 478935-29-4 The following contents are mentioned in the article:

An effective and economical protocol was developed for the synthesis of 3-substituted indoles by one-pot three-component coupling reaction of a substituted salicylaldehyde, N-methylaniline and indole using [Hmim] HSO4 as a catalyst. All the synthesized derivatives were evaluated for inhibition of cancer cell. The initial assays indicated that some of the newly synthesized compounds displayed significantly good inhibition activities against human breast cancer cell (MCF7), cell lines compared with the control (Adriamysin), which might be developed as novel lead scaffold for potential anticancer agents. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Application of 478935-29-4).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.Application of 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Synthesis of diethyl maleate catalyzed by acid functionalized ionic liquids was written by Yu, Dan;Guo, Hongyun. And the article was included in Gongye Cuihua in 2009.Reference of 478935-29-4 The following contents are mentioned in the article:

Di-Et maleate was obtained by a reaction of maleic anhydride and anhydrous ethanol in the presence of an ionic liquid [i.e., TEAPS sulfate, N,N,N-triethyl-3-sulfo-1-propanaminium sulfate (1:1)]. Factors influencing the product formation were confirmed and the above-mentioned Di-Et maleate [i.e., (2Z)-2-butenedioic acid 1,4-di-Et ester, 99% yield] was obtained under the following reaction conditions : n(maleic anhydride) : n(ethanol) = 1:4, dosage of ionic liquid = 20% (wt) of maleic anhydride, cyclohexane as water carrier, 115°, reflux and water segregation for 4 h. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Reference of 478935-29-4).

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.Reference of 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Regioselectivity for nitrochlorobenzene preparation over imidazolium ionic liquids media using nitric acid was written by Gong, D.;Peng, X.;Sun, Z.. And the article was included in Asian Journal of Chemistry in 2010.Related Products of 478935-29-4 The following contents are mentioned in the article:

Nitrochlorobenzene was regioselectively prepared over imidazolium ionic liquids media by using HNO₃ as nitrating agent. A variety of ionic liquids, [Hmim]HSO₄, [Hmim]NO₃ and [Hmim]CF₃CO₂ (Hmim = 1-methylimidazolium) were prepared for the improvement of regioselectivity in preparation of mononitrochlobenzene isomers. A high amount of para isomer was achieved when employing [Hmim]HSO₄. Ionic liquids were conveniently reused for five times by filtration with excellent yield of mono-nitration products and para-selectivity. 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. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division.Related Products of 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Catalyzed esterifications in room temperature ionic liquids with acidic counteranion as recyclable reaction media was written by Fraga-Dubreuil, Joan;Bourahla, Khadidja;Rahmouni, Mustapha;Bazureau, Jean Pierre;Hamelin, Jack. And the article was included in Catalysis Communications in 2002.Product Details of 478935-29-4 The following contents are mentioned in the article:

Esterification reactions of acetic acid, methoxyacetic acid and methylmalonic acid with neo-pentanol, hexanol, heptanol and decanol have been investigated in three ionic liquids with hydrogen sulfate, dihydrogen phosphate as counteranions and also two ionic liquids modified with HPF₆ as catalyst. The nature of both the counteranion and cation influence the behavior of the catalyst. Good yields and high selectivities were obtained and all the produced esters could be easily recovered due to their immiscibility with the ionic liquid as green reaction medium. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Product Details of 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. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Product Details of 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Efficient Combination of Recyclable Task Specific Ionic Liquid and Microwave Dielectric Heating for the Synthesis of Lipophilic Esters was written by Arfan, Atef;Bazureau, Jean Pierre. And the article was included in Organic Process Research & Development in 2005.SDS of cas: 478935-29-4 The following contents are mentioned in the article:

Mild and efficient esterification reactions of carboxylic acids with neo-pentanol were carried out using task-specific ionic liquids with hydrogen sulfate counter-anion under microwave irradiation The latent acidity of the ionic liquid was introduced by anion metathesis from hydrogen sulfate with the corresponding imidazolium or pyridinium halides. The catalyst [C₄mim][HSO₄] modified with 5% of concentrated sulfuric acid was reused three times without considerable loss of activity in esterification using classical heating in oil bath. 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. 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.SDS of cas: 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Oxidation of cyclooctene to suberic acid using perrhenate-containing composite ionic liquids as green catalysts was written by Wang, J. Y.;Zhou, M. D.;Yuan, Y. G.;Fu, N. H.;Zang, S. L.. And the article was included in Russian Journal of General Chemistry in 2015.Synthetic Route of C10H20N2O4S The following contents are mentioned in the article:

A series of quaternary ammonium perrhenate/3-hexyl-1-methyl-imidazolium hydrogen sulfate ([Hmim]HSO₄) composite ionic liquids has been prepared For the first time, the composite ionic liquids are used both as catalyst and solvent in oxidation of cyclooctene to suberic acid in the presence of hydrogen peroxide as a green oxidant. It was found that organic perrhenate salts play the important role in improving the selectivity of cyclooctene oxidation to suberic acid. The yield of suberic acid under the mild conditions is from good to high. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Synthetic Route of C10H20N2O4S).

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. 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. Synthetic Route of C10H20N2O4S

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

A novel protic ionic liquid/silica gel electrolyte and its properties was written by Wang, Zan;Liu, Yan;Liu, Hongtao. And the article was included in Zhongguo Kexue: Huaxue in 2012.Formula: C10H20N2O4S The following contents are mentioned in the article:

A novel protic ionic liquid/silica gel electrolyte has been prepared by in-situ one-step sol-gel method. The as-prepared proton-conductivity composite gel electrolyte is smooth, transparent, and flexible. It is shown that this composite gel electrolyte has good thermal stability (>300°C), wide electrochem. window (>2.8 V), and high proton conductivity (11.25×10^-3 S cm^-1, 80°C). It is expected to use the as-prepared proton-enhancing gel electrolyte for advanced energy-storage applications. 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. 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 This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Formula: C10H20N2O4S

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Electrowetting based infrared lens using ionic liquids was written by Hu, Xiaodong;Zhang, Shiguo;Liu, Yu;Qu, Chao;Lu, Liujin;Ma, Xiangyuan;Zhang, Xiaoping;Deng, Youquan. And the article was included in Applied Physics Letters in 2011.Formula: C10H20N2O4S The following contents are mentioned in the article:

IR variable focus ionic liquids lenses using electrowetting have been developed. Such lenses could overcome the problems caused by use of water, e.g., evaporation and poor thermostability, while keeping good optical transparency in visible light and near-IR region. Convex and concave lenses could be tuned by applied voltage or refractive index of ILs used, and the transmittance exceeded 90% over the spectrum of visible light and near-IR. (c) 2011 American Institute of Physics. 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. 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.Formula: C10H20N2O4S

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Efficient and convenient oxidation of sulfides to sulfones using H₂O₂ catalyzed by V₂O₅ in ionic liquid [C₁₂mim][HSO₄] was written by Hu, Yu-Lin;Liu, Xiao-Bing;Fang, Dong. And the article was included in Catalysis Science & Technology in 2014.Recommanded Product: 478935-29-4 The following contents are mentioned in the article:

A simple, efficient, and eco-friendly procedure for the oxidation of sulfides to sulfones using H₂O₂ catalyzed by V₂O₅ in ionic liquid [C₁₂mim][HSO₄] has been developed. This atom-economical protocol affords the target products in good to high yields. The products can be separated by a simple extraction with organic solvent, and the catalytic system can be recycled and reused without loss of 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 is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. Imidazole also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes.Recommanded Product: 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Oxidation of benzylic alcohols to their corresponding carbonyl compounds using ceric ammonium nitrate (CAN)/bronsted acidic ionic liquid was written by Hajipour, A. R.;Khazdooz, L.;Ruoho, A. E.. And the article was included in Journal of the Iranian Chemical Society in 2011.Synthetic Route of C10H20N2O4S The following contents are mentioned in the article:

A chemoselective and efficient procedure for the oxidation of alcs. to the corresponding carbonyl compounds is reported using ceric ammonium nitrate in the presence of 3-hexyl-1-methylimidazolium hydrogen sulfate as Bronsted acidic ionic liquid ([Hmim]HSO₄) as the solvent under mild conditions. The use of non-toxic 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: 478935-29-4Synthetic Route of 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 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).Synthetic Route of C10H20N2O4S

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem