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(2-氧代-2-苯乙基)膦酸二乙酯_分子结构_CAS_3453-00-7)
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(2-氧代-2-苯乙基)膦酸二乙酯

产品号 410756 公司名称 Sigma Aldrich
CAS号 3453-00-7 公司网站 http://www.sigmaaldrich.com
分子式 C12H17O4P 电 话 1-800-521-8956
分子量 256.234741 传 真
纯 度 97% 电子邮件
保 存 Chembase数据库ID: 74939

产品价格信息

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产品别名

标题
Diethyl (2-oxo-2-phenylethyl)phosphonate
IUPAC标准名
diethyl (2-oxo-2-phenylethyl)phosphonate
IUPAC传统名
diethyl 2-oxo-2-phenylethylphosphonate
别名
NSC 648426
Diethyl phenacylphosphonate
Diethyl benzoylmethylphosphonate

产品登记号

CAS号 3453-00-7
PubChem SID 24865704
MDL号 MFCD00015342

产品性质

线性分子式 C6H5COCH2P(O)(OC2H5)2
纯度 97%
沸点 192-193 °C/11 mmHg(lit.)
密度 1.179 g/mL at 25 °C(lit.)
闪点 >113 °C
闪点 >235.4 °F
折射率 n20/D 1.513(lit.)
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个人保护装置 Eyeshields, Gloves
德国WGK号 3

产品详细信息

详细说明 (English)
Packaging
1, 10 g in glass bottle
Application
Reactant involved in:
• Asymmetric Michael addition of β-oxo phosphonates to nitro olefins1
• Gem-chlorofluorination of keto phosphonates with subsequent functionalization of the products2
• Cyclocondensation reactions to produce arylphosphonates3
• Diazo transfer reactions for synthesis of diazo-phosphonyl compounds4
• Horner-Wadsworth-Emmons reactions5
• Inverse-electron-demand Diels-Alder reactions6
详细说明 (简体中文)
包装
1, 10 g in glass bottle
Application
Reactant involved in:
• Asymmetric Michael addition of β-oxo phosphonates to nitro olefins1
• Gem-chlorofluorination of keto phosphonates with subsequent functionalization of the products2
• Cyclocondensation reactions to produce arylphosphonates3
• Diazo transfer reactions for synthesis of diazo-phosphonyl compounds4
• Horner-Wadsworth-Emmons reactions5
• Inverse-electron-demand Diels-Alder reactions6

参考文献