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反式-2-(3-氟苯基)乙烯基硼酸_分子结构_CAS_849062-22-2)
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反式-2-(3-氟苯基)乙烯基硼酸

产品号 637971 公司名称 Sigma Aldrich
CAS号 849062-22-2 公司网站 http://www.sigmaaldrich.com
分子式 C8H8BFO2 电 话 1-800-521-8956
分子量 165.9573232 传 真
纯 度 电子邮件
保 存 Chembase数据库ID: 142226

产品价格信息

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产品别名

标题
trans-2-(3-Fluorophenyl)vinylboronic acid
IUPAC标准名
[(E)-2-(3-fluorophenyl)ethenyl]boronic acid
IUPAC传统名
(E)-2-(3-fluorophenyl)ethenylboronic acid
别名
(E)-2-(3-Fluorophenyl)ethenylboronic acid

产品登记号

PubChem SID 24882901
MDL号 MFCD06008297
CAS号 849062-22-2

产品性质

Empirical Formula (Hill Notation) C8H8FBO2
熔点 184-186 °C(lit.)
MSDS下载 下载链接
德国WGK号 3

产品详细信息

详细说明 (English)
Packaging
1, 5 g in glass bottle
Application
Reactant for:
• Enantioselective diastereoselective synthesis of tetracyclins via metal-catalyzed ring opening of meso-oxabicyclic alkenes followed by hydrogenation and Friedel-Crafts alkylation1
• Palladium-catalyzed Suzuki-Miyaura coupling reactions2
• Preparation of anticonvulsant agents3
• Preparation of piperazinyl pyrimidylhydroxamic acid deriatives as histone deacetylase inhibitors and antitumor agents4
• Preparation of ethyl-substituted conjugated dienoates and dienones by stereoselective Suzuki cross-coupling5
详细说明 (简体中文)
包装
1, 5 g in glass bottle
Application
Reactant for:
• Enantioselective diastereoselective synthesis of tetracyclins via metal-catalyzed ring opening of meso-oxabicyclic alkenes followed by hydrogenation and Friedel-Crafts alkylation1
• Palladium-catalyzed Suzuki-Miyaura coupling reactions2
• Preparation of anticonvulsant agents3
• Preparation of piperazinyl pyrimidylhydroxamic acid deriatives as histone deacetylase inhibitors and antitumor agents4
• Preparation of ethyl-substituted conjugated dienoates and dienones by stereoselective Suzuki cross-coupling5

参考文献