二乙基膦酰基乙酸叔丁酯

• 产品号: 348333
• CAS号: 27784-76-5
• 分子式: C10H21O5P
• 分子量: 252.244501
• 纯 度: 95%

产品别名

• 标题: tert-Butyl diethylphosphonoacetate
• IUPAC标准名: tert-butyl 2-(diethoxyphosphoryl)acetate
• IUPAC传统名: tert-butyl 2-(diethoxyphosphoryl)acetate
• 别名: tert-Butyl (diethoxyphosphinyl)acetate; (Diethoxyphosphinyl)acetic acid 1,1-dimethylethyl ester; Diethyl tert-butoxycarbonylmethanephosphonate

产品登记号

• CAS号: 27784-76-5
• PubChem SID: 24861567
• MDL号: MFCD00075414

产品性质

• 线性分子式: (C2H5O)2P(O)CH2CO2C(CH3)3
• 纯度: 95%
• 沸点: 100-103 °C/1.5 mmHg(lit.)
• 密度: 1.074 g/mL at 25 °C(lit.)
• 闪点: >113 °C
• 闪点: >235.4 °F
• 折射率: n20/D 1.431(lit.)
• 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
5 g in glass bottle
Application
Reactant for:
• Preparation of ydroxymethylated dihydroxyvitamin D3 analogs via Wittig-Horner approach, as potential antitumor agents1
• Synthesis of phosphopeptide mimetic prodrugs targeted to Src homology 2 (SH2) domain of signal transducer and activator of transcription 3 (Stat 3)2
• One-pot synthesis of the DPP4-selective inhibitor ABT-341 by a four-component coupling mediated by a diphenylprolinol silyl ether3
• Bicyclic triaminophosphine-promoted stereoselective synthesis of a,β-unsaturated esters, fluorides, and nitriles from aldehydes and ketones using Wadsworth-Emmons phosphonates4
• Preparation of amidopropenyl hydroxamates as human histone deacetylase (HDAC) inhibitors5

详细说明 (简体中文)

包装
5 g in glass bottle
Application
Reactant for:
• Preparation of ydroxymethylated dihydroxyvitamin D3 analogs via Wittig-Horner approach, as potential antitumor agents1
• Synthesis of phosphopeptide mimetic prodrugs targeted to Src homology 2 (SH2) domain of signal transducer and activator of transcription 3 (Stat 3)2
• One-pot synthesis of the DPP4-selective inhibitor ABT-341 by a four-component coupling mediated by a diphenylprolinol silyl ether3
• Bicyclic triaminophosphine-promoted stereoselective synthesis of a,β-unsaturated esters, fluorides, and nitriles from aldehydes and ketones using Wadsworth-Emmons phosphonates4
• Preparation of amidopropenyl hydroxamates as human histone deacetylase (HDAC) inhibitors5