2-(Bromoacetyl)benzofuran

• Catalog No.: 715670
• CAS Number: 23489-36-3
• M. F.: C10H7BrO2
• M. W.: 239.06538
• Purity: 97%

SYNONYMS

• Title: 2-(溴乙酰基)苯并呋喃
• IUPAC name: 1-(1-benzofuran-2-yl)-2-bromoethan-1-one
• IUPAC Traditional name: 1-(1-benzofuran-2-yl)-2-bromoethanone
• Synonyms: 1-(1-Benzofuran-2-yl)-2-bromoethan-1-one; 2-(Bromoacetyl)benzo[b]furan; 1-(Benzofuran-2-yl)-2-bromoethanone; 2-Benzofuranyl bromomethyl ketone; 2-(2-Bromoacetyl)benzofuran; 1-(Benzo[b]furan-2-yl)-2-bromoethan-1-one; 1-(1-Benzofuran-2-yl)-2-bromoethanone; 1-(2-Benzofuryl)-2-bromo-1-ethanone; 1-Benzo[b]furan-2-yl-2-bromoethanone; 2-Benzofuryl bromomethyl ketone

DATABASE IDS

• MDL Number: MFCD00176644
• CAS Number: 23489-36-3

PROPERTIES

• Empirical Formula (Hill Notation): C10H7BrO2
• Purity: 97%
• Melting Point: 86-90 °C
• GHS Signal Word: Danger
• GHS Hazard statements: H302-H314
• European Hazard Symbols: Corrosive (C)
• GHS Precautionary statements: P280-P305 + P351 + P338-P310
• RID/ADR: UN 3261 8/PG 3
• Risk Statements: 22-34
• Safety Statements: 26-36/37/39-45
• Hazard Class: 8
• UN Number: 3261
• Packing Group: 3
• German water hazard class: 2

DETAILS

Description (简体中文)

包装
1 g in glass bottle
Application
Reactant for:
• Eschenmoser coupling reaction1
• Preparation of β-oxo sulfones as substrates for stereoselective Michael addition/cross-benzoin cascade reactions2
• Preparation of thienylpyrazole-based thiazoles and pyrazolines as antimicrobial, antioxidant, anti-inflammatory, and analgesic agents3
• Preparation of isatin-(benzofuryl-thiazolyl)-hydrazones by cyclocondensation with isatin-thiosemicarbazones under microwave irradiation as antimicrobial agents4
• Synthesis of 2-naphthyl ethers as a protective agent against DNA damage induced by bleomycin-iron5
• Asymmetric synthesis of β-dialkylamino alcohols by Ru-catalyzed transfer hydrogenation of α-dialkylamino ketones6

Description (English)

Packaging
1 g in glass bottle
Application
Reactant for:
• Eschenmoser coupling reaction1
• Preparation of β-oxo sulfones as substrates for stereoselective Michael addition/cross-benzoin cascade reactions2
• Preparation of thienylpyrazole-based thiazoles and pyrazolines as antimicrobial, antioxidant, anti-inflammatory, and analgesic agents3
• Preparation of isatin-(benzofuryl-thiazolyl)-hydrazones by cyclocondensation with isatin-thiosemicarbazones under microwave irradiation as antimicrobial agents4
• Synthesis of 2-naphthyl ethers as a protective agent against DNA damage induced by bleomycin-iron5
• Asymmetric synthesis of β-dialkylamino alcohols by Ru-catalyzed transfer hydrogenation of α-dialkylamino ketones6