物质信息
ID:321344
名称和标识
IUPAC传统名
1-(1-benzofuran-2-yl)-2-bromoethanone
IUPAC标准名
1-(1-benzofuran-2-yl)-2-bromoethan-1-one
别名
1-(Benzofuran-2-yl)-2-bromoethanone1-Benzo[b]furan-2-yl-2-bromoethanone2-Benzofuranyl bromomethyl ketone2-(2-Bromoacetyl)benzofuran1-(Benzo[b]furan-2-yl)-2-bromoethan-1-one2-Benzofuryl bromomethyl ketone2-(溴乙酰基)苯并呋喃1-(1-Benzofuran-2-yl)-2-bromoethanone2-(Bromoacetyl)benzo[b]furan2-(Bromoacetyl)benzofuran1-(1-Benzofuran-2-yl)-2-bromoethan-1-one1-(2-Benzofuryl)-2-bromo-1-ethanone
化合物性质
安全信息
GHS警示词
Danger
MSDS下载
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
联合国危险货物等级
8
联合国危险货物编号
3261
德国WGK号
2
GHS危险品标识
腐蚀金属，类别1
腐蚀皮肤，类别1A，1B，1C
严重眼损伤，类别1
急性毒性（口服，皮肤接触，吸入），类别4
皮肤刺激，类别2
眼刺激，类别2
皮肤过敏，类别1
特定目标器官毒性 -一次接触，类别3
安全公开号
26-36/37/39-45
联合国危险货物包装类别(PG)
3
欧盟危险性物质标志
腐蚀性 (C)GHS危险声明
H302-H314
产品相关信息
Empirical Formula (Hill Notation)
C10H7BrO2
纯度
97%
理化性质
熔点
86-90 °C
描述信息
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
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
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