Home > Compound List > Product Information
2-Bromo-3′-hydroxyacetophenone_Molecular_structure_CAS_2491-37-4)
Click picture or here to close

2-Bromo-3′-hydroxyacetophenone

Catalog No. 594709 Name Sigma Aldrich
CAS Number 2491-37-4 Website http://www.sigmaaldrich.com
M. F. C8H7BrO2 Telephone 1-800-521-8956
M. W. 215.04398 Fax
Purity Email
Storage Chembase ID: 75365

SYNONYMS

Title
2-溴-3′-羟基苯乙酮
IUPAC name
2-bromo-1-(3-hydroxyphenyl)ethan-1-one
IUPAC Traditional name
2-bromo-1-(3-hydroxyphenyl)ethanone

DATABASE IDS

MDL Number MFCD05664326
CAS Number 2491-37-4
PubChem SID 24881530

PROPERTIES

Empirical Formula (Hill Notation) C8H7BrO2
Melting Point 70-74 °C(lit.)
GHS Pictograms GHS05
GHS Pictograms GHS07
GHS Signal Word Danger
GHS Hazard statements H302-H314-H317
European Hazard Symbols Corrosive Corrosive (C)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
GHS Precautionary statements P280-P305 + P351 + P338-P310
RID/ADR UN 3263 8/PG 2
Risk Statements 22-34-43
Safety Statements 26-36/37/39-45
Hazard Class 8
UN Number 3263
Packing Group 2
German water hazard class 3

DETAILS

Description (English)
Packaging
1, 5 g in glass bottle
Application
Reactant involved in the synthesis of:
• Pyrrole-3-carboxylic acids1
• N-aryl-N-thiazolyl compounds via the Hantzsch reaction2
• Disubstituted oxadiazolylindole derivatives with antiinflammatory, analgesic and nitric oxide releasing activity3
• Anilino-aryl-thiazoles with inhibitory activity toward valosin-containing proteins4
• Tyrosine kinase erythropoietin inhibitors5
• E. coli methionine aminopeptidase inhibitors6
Description (简体中文)
包装
1, 5 g in glass bottle
Application
Reactant involved in the synthesis of:
• Pyrrole-3-carboxylic acids1
• N-aryl-N-thiazolyl compounds via the Hantzsch reaction2
• Disubstituted oxadiazolylindole derivatives with antiinflammatory, analgesic and nitric oxide releasing activity3
• Anilino-aryl-thiazoles with inhibitory activity toward valosin-containing proteins4
• Tyrosine kinase erythropoietin inhibitors5
• E. coli methionine aminopeptidase inhibitors6

REFERENCES