655230-45-8

Basic information

• Product Name: Benzenemethanol, 2-azido-5-bromo-
• CAS NO: 655230-45-8
• Molecular Formula: C7H6BrN3O
• Molecular Weight: 228.048
• Mol File: 655230-45-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 2-azido-5-bromo-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 2-azido-5-bromo-(655230-45-8)
• EPA Substance Registry System: Benzenemethanol, 2-azido-5-bromo-(655230-45-8)

Safety Data

• Hazardous Substances Data: 655230-45-8(Hazardous Substances Data)

Usage

General Description

Benzenemethanol, 2-azido-5-bromo- is a chemical compound with the molecular formula C7H6BrN3O. It is an azide compound with a benzene ring and a bromine atom attached to the benzene ring. Benzenemethanol, 2-azido-5-bromo- is commonly used in the synthesis of pharmaceuticals, agrochemicals, and organic materials. It is also used in the research and development of new chemical compounds and materials. Benzenemethanol, 2-azido-5-bromo- is known for its potential uses in various chemical reactions and its role in the development of new products in the pharmaceutical and chemical industries.

Upstream product

• 5344-90-1 2-Aminobenzyl alcohol 
• 1001621-59-5 2-azido-5-bromobenzaldehyde 
• 93777-26-5 5-bromo-2-fluorobenzaldehyde 
• 20712-12-3 (2-amino-5-bromophenyl)methanol 
• 20615-76-3 2-azidobenzyl alcohol 

Downstream Products

• 1245786-13-3 2-azido-5-bromobenzyl methanesulfonate 
• 1001621-59-5 2-azido-5-bromobenzaldehyde 
• 655230-14-1 dithiocarbonic acid O-ethyl ester S-(5-bromo-2-triphenylphosphoranylideneamino)benzyl ester 
• 566942-93-6 dithiocarbonic acid S-(5-bromo-2-diphenylvinylideneamino-benzyl) ester O-ethyl ester 
• 655229-97-3 dithiocarbonic acid O-ethyl ester S-(2-azido-5-bromobenzyl) ester 
• 655229-87-1 2-azido-5-bromobenzyl bromide 

Relevant articles and documents

FUSED QUADRACYCLIC COMPOUNDS, COMPOSITIONS AND USES THEREOF

Provided herein are substituted fused quadracyclic compounds useful as inhibitors of MK2. The invention further provides pharmaceutical compositions of the compounds of the invention. The invention also provides medical uses of substituted fused quadracyclic compounds.

Design, synthesis, and in vitro pharmacology of new radiolabeled γ-hydroxybutyric acid analogues including photolabile analogues with irreversible binding to the high-affinity γ-hydroxybutyric acid binding sites

γ-Hydroxybutyric acid (GHB) is a psychotropic compound endogenous to the brain. Despite its potential physiological significance, the complete molecular mechanisms of action remain unexplained. To facilitate the isolation and identification of the high-affinity GHB binding site, we herein report the design and synthesis of the first 125I-labeled radioligands in the field, one of which contains a photoaffinity label which enables it to bind irreversibly to the high-affinity GHB binding sites.