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苄基(三苯基膦)乙酸酯_分子结构_CAS_15097-38-8)
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苄基(三苯基膦)乙酸酯

产品号 419206 公司名称 Sigma Aldrich
CAS号 15097-38-8 公司网站 http://www.sigmaaldrich.com
分子式 C27H23O2P 电 话 1-800-521-8956
分子量 410.444081 传 真
纯 度 97% 电子邮件
保 存 Chembase数据库ID: 148623

产品价格信息

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产品别名

标题
Benzyl(triphenylphosphoranylidene)acetate
IUPAC标准名
benzyl 2-(triphenyl-λ5-phosphanylidene)acetate
IUPAC传统名
benzyl 2-(triphenyl-λ5-phosphanylidene)acetate
别名
2-(Triphenylphosphoranylidene)acetic acid phenylmethyl ester
(Benzyloxycarbonylmethylene)triphenylphosphorane

产品登记号

MDL号 MFCD00191787
PubChem SID 24866098
CAS号 15097-38-8

产品性质

线性分子式 (C6H5)3P=CHCO2CH2C6H5
纯度 97%
熔点 120-122 °C(lit.)
MSDS下载 下载链接
个人保护装置 Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
德国WGK号 3

产品详细信息

详细说明 (English)
Packaging
5, 25 g in glass bottle
Application
Reactant for:
• Tributylphosphine-mediated vinylogous Wittig reactions1
• Synthesis of 1,2-dioxanes for antitrypanosomal activity2
• Organocatalytic Michael-type reactions / Wittig reactions of phosphorus ylides and unsaturated ketones3
• Stereoselective phosphine-catalyzed cycloaddition to form spirocyclopenteneoxindoles4
• Enantioselective synthesis of pantothenic acid5
• Preparation of phosphorus ylides from phosphoranes and acetic anhydride6
详细说明 (简体中文)
包装
5, 25 g in glass bottle
Application
Reactant for:
• Tributylphosphine-mediated vinylogous Wittig reactions1
• Synthesis of 1,2-dioxanes for antitrypanosomal activity2
• Organocatalytic Michael-type reactions / Wittig reactions of phosphorus ylides and unsaturated ketones3
• Stereoselective phosphine-catalyzed cycloaddition to form spirocyclopenteneoxindoles4
• Enantioselective synthesis of pantothenic acid5
• Preparation of phosphorus ylides from phosphoranes and acetic anhydride6

参考文献