2-膦酰丙酸三乙酯

• 产品号: 174653
• CAS号: 3699-66-9
• 分子式: C9H19O5P
• 分子量: 238.217921
• 纯 度: 98%

产品别名

• 标题: Triethyl 2-phosphonopropionate
• IUPAC标准名: ethyl 2-(diethoxyphosphoryl)propanoate
• IUPAC传统名: ethyl 2-(diethoxyphosphoryl)propanoate
• 别名: 2-(Diethoxyphosphoryl)propionic acid ethyl ester

产品登记号

• Beilstein号: 1786994
• MDL号: MFCD00009159
• EC号: 223-033-4
• CAS号: 3699-66-9
• PubChem SID: 24850353

产品性质

• 线性分子式: (C2H5O)2P(O)CH(CH3)CO2C2H5
• 纯度: 98%
• 沸点: 143-144 °C/12 mmHg(lit.)
• 密度: 1.111 g/mL at 25 °C(lit.)
• 闪点: 89 °C
• 闪点: 192.2 °F
• 折射率: n20/D 1.431(lit.)
• 个人保护装置: Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
• 德国WGK号: 3

产品详细信息

详细说明 (English)

Packaging
10, 50 g in glass bottle
Application
Reactant involved in:
• Intramolecular conjugate addition for the synthesis of floresolide B1
• Chemoenzymatic one-pot synthesis of γ-butyrolactones2
• Enantioselective synthesis of spiroindane di-Me acetic acid via asymmetric hydrogenation3
• Stereoselective intramolecular Diels-Alder reactions4,5
• Horner-Wadsworth-Emmons reactions6
This Wittig-Horner reagent condenses with a wide variety of aldehydes and ketones to form acrylates.

详细说明 (简体中文)

包装
10, 50 g in glass bottle
Application
Reactant involved in:
• Intramolecular conjugate addition for the synthesis of floresolide B1
• Chemoenzymatic one-pot synthesis of γ-butyrolactones2
• Enantioselective synthesis of spiroindane di-Me acetic acid via asymmetric hydrogenation3
• Stereoselective intramolecular Diels-Alder reactions4,5
• Horner-Wadsworth-Emmons reactions6
该 Wittig-Horner 试剂可与各种醛和酮发生缩合反应形成丙烯酸酯。