2-(溴乙酰基)苯并呋喃

• 产品号: 715670
• CAS号: 23489-36-3
• 分子式: C10H7BrO2
• 分子量: 239.06538
• 纯 度: 97%

产品别名

• 标题: 2-(Bromoacetyl)benzofuran
• IUPAC标准名: 1-(1-benzofuran-2-yl)-2-bromoethan-1-one
• IUPAC传统名: 1-(1-benzofuran-2-yl)-2-bromoethanone
• 别名: 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

产品登记号

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

产品性质

• Empirical Formula (Hill Notation): C10H7BrO2
• 纯度: 97%
• 熔点: 86-90 °C
• GHS警示词: Danger
• GHS危险声明: H302-H314
• 欧盟危险性物质标志: 腐蚀性(Corrosive) (C)
• GHS警示性声明: P280-P305 + P351 + P338-P310
• RID/ADR: UN 3261 8/PG 3
• 危险公开号: 22-34
• 安全公开号: 26-36/37/39-45
• 联合国危险货物等级: 8
• 联合国危险货物编号: 3261
• 联合国危险货物包装类别(PG): 3
• 德国WGK号: 2

产品详细信息

详细说明 (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

详细说明 (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