220364-22-7

Basic information

• Product Name: [3-(4-BROMO-BENZYL)-3H-IMIDAZOL-4-YL]-METHANOL
• Synonyms: [3-(4-BROMO-BENZYL)-3H-IMIDAZOL-4-YL]-METHANOL;1-(4-BroMobenzyl)-5-hydroxyMethyliMidazole;1-[(4-Bromophenyl)methyl]-1H-imidazole-5-methanol;(1-(4-bromobenzyl)-1H-imidazol-5-yl)methanol
• CAS NO: 220364-22-7
• Molecular Formula: C₁₁H₁₁BrN₂O
• Molecular Weight: 267.12
• Mol File: 220364-22-7.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: [3-(4-BROMO-BENZYL)-3H-IMIDAZOL-4-YL]-METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: [3-(4-BROMO-BENZYL)-3H-IMIDAZOL-4-YL]-METHANOL(220364-22-7)
• EPA Substance Registry System: [3-(4-BROMO-BENZYL)-3H-IMIDAZOL-4-YL]-METHANOL(220364-22-7)

Safety Data

• Hazardous Substances Data: 220364-22-7(Hazardous Substances Data)

Usage

General Description

[3-(4-BROMO-BENZYL)-3H-IMIDAZOL-4-YL]-METHANOL is a chemical compound with the molecular formula C11H11BrN2O. It is a benzyl-substituted imidazole derivative with a methanol group. [3-(4-BROMO-BENZYL)-3H-IMIDAZOL-4-YL]-METHANOL is used in pharmaceutical research and drug development due to its potential as a pharmacological agent. It may have applications in the treatment of various medical conditions and diseases, and its structure and properties make it an important target for drug design and synthesis. Its unique combination of functional groups makes it an interesting target for further study and development in the field of medicinal chemistry.

Upstream product

• 62147-49-3 1,3-dihydroxyacetone dimer 
• 333-20-0 potassium thioacyanate 
• 26177-44-6 4-bromobenzylamine hydrochloride 
• 312936-77-9 1-(4-Bromobenzyl)-2-Mercapto-5-Hydroxymethylimidazole 
• 108-20-3 di-isopropyl ether 
• 12440-03-8 vanadium(IV) oxide sulfate hydrate 
• 106-40-1 4-bromo-aniline 

Downstream Products

• 488831-44-3 [3-(4'-fluoro-biphenyl-4-ylmethyl)-3H-imidazol-4-yl]-methanol 
• 488831-39-6 [3-(4'-chloro-biphenyl-4-ylmethyl)-3H-imidazol-4-yl]-methanol 
• 488831-42-1 [3-(3',5'-dichloro-biphenyl-4-ylmethyl)-3H-imidazol-4-yl]-methanol 
• 238765-02-1 3-(4-bromo-benzyl)-3H-imidazole-4-carbaldehyde 
• 742045-40-5 1-(4-bromobenzyl)-5-(chloromethyl)-1H-imidazole 
• 238764-78-8 3-(4'-chloro-biphenyl-4-ylmethyl)-3H-imidazole-4-carbaldehyde 
• 238764-71-1 3-(4'-fluoro-biphenyl-4-ylmethyl)-3H-imidazole-4-carbaldehyde 
• 312936-83-7 4-(1-[(4-bromophenyl)methyl]imidazol-5-ylmethyl)-1-(3-chlorophenyl)piperazin-2-one 
• 1417526-55-6 2-(hydroxymethyl)-1-((4'-(trifluoromethyl)biphenyl-4-yl)methyl)-1H-imidazole-5-carbaldehyde 

Relevant articles and documents

A Continuous-Flow Method for the Desulfurization of Substituted Thioimidazoles Applied to the Synthesis of Etomidate Derivatives

A simple yet robust flow set-up for the efficient desulfurization of a series of thioimidazoles is presented, which generates the corresponding imidazole derivatives in high yields. The strategic choice of peristaltic over piston pumps allowed reliable delivery of the heterogeneous stream of the thioimidazole substrate into a T-piece where it reacted with NaNO2 in the presence of acetic acid. This approach enabled the controlled and safe formation of the reactive nitrosonium species without uncontrolled exposure to hazardous nitrous oxide by-products as observed in related batch protocols. The value of the resulting imidazole products was further demonstrated by their conversion into various esters representing new derivatives of the known analgesic etomidate through an efficient one-pot Corey–Gilman–Ganem oxidation procedure.

AZOLE HETEROCYCLIC COMPOUND, PREPARATION METHOD, PHARMACEUTICAL COMPOSITION AND USE

The present invention relates to the field of pharmaceutical chemistry, and in particular, to a novel class of azole compounds represented by general formula (I), (II) or (III) and a preparation method thereof, a pharmaceutical composition with the compounds as active components, and a use of the azole compounds and the pharmaceutical composition in the preparation of a medicament for treatment of diseases associated with Lp-PLA2 enzyme activities, wherein each substituent is as defined in the specification.

Process for preparing a 1-substituted 5-hydroxymethyl imidazole

A process for preparing a 1-substituted 5-hydroxymethylimidazole of the formula: , wherein R represents alkyl, hydroxyalkyl, allyl, or substituted or unsubstituted arylmethyl or diarylmethyl, comprising the step of reacting a 1-substituted 2-mercapto-5-hy