Substance
ID:314985
Names and Identifiers
IUPAC Traditional name
2-bromo-1-(3-hydroxyphenyl)ethanone
IUPAC name
2-bromo-1-(3-hydroxyphenyl)ethan-1-one
Synonyms
2-Bromo-3′-hydroxyacetophenone2-溴-3′-羟基苯乙酮
Properties
Physical Property
Melting Point
70-74 °C(lit.)
Safety Information
RID/ADR
UN 3263 8/PG 2
GHS Precautionary statements
P280-P305+P351+P338-P310
Risk Statements
22-34-43
UN Number
3263
GHS Hazard statements
H302-H314-H317
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
Packing Group
2
European Hazard Symbols
Corrosive (C)Hazard Class
8
GHS Signal Word
Danger
GHS Pictograms
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
MSDS Link
Safety Statements
26-36/37/39-45
German water hazard class
3
Product Information
Empirical Formula (Hill Notation)
C8H7BrO2
Molecule Details
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
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
Molecular Spectra
No Data Available
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References
No Data Available
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