(2-氧代庚基)膦酸二甲酯

• 产品号: 157937
• CAS号: 36969-89-8
• 分子式: C9H19O4P
• 分子量: 222.218521
• 纯 度: 85%

产品别名

• 标题: Dimethyl 2-oxoheptylphosphonate
• IUPAC标准名: dimethyl (2-oxoheptyl)phosphonate
• IUPAC传统名: dimethyl 2-oxoheptylphosphonate
• 别名: (2-Oxoheptyl)phosphonic acid dimethyl ester; Dimethyl (hexanoylmethyl)phosphonate

产品登记号

• Beilstein号: 1946305
• CAS号: 36969-89-8
• MDL号: MFCD00009514
• EC号: 253-293-4
• PubChem SID: 24849710

产品性质

• 级别: technical grade
• 线性分子式: CH3(CH2)4COCH2P(O)(OCH3)2
• 纯度: 85%
• 沸点: 109 °C/0.4 mmHg(lit.)
• 密度: 1.07 g/mL at 25 °C(lit.)
• 闪点: 110 °C
• 闪点: 230 °F
• 折射率: n20/D 1.444(lit.)
• 个人保护装置: Eyeshields, Gloves, half-mask respirator (US), multi-purpose combination respirator cartridge (US)
• 德国WGK号: 3

产品详细信息

详细说明 (简体中文)

Application
前列腺素合成的关键中间体。
Reactant for:
• Beirut reaction for the preparation of phosphonylated quinoxaline dioxides1
• Preparation of pyrrolomorphinan derivatives as κ opioid agonists via cyclocondensation, Vilsmeier-Haack formylation, Horner-Wadsworth-Emmons reaction, and Kocienski-modified Julia olefination from naltrexone methyl ether2
• Synthesis of C-glycosides amphiphiles via solvent-free Horner-Wadsworth-Emmons reaction with unprotected sugars3
• Preparation of specific inhibitors of endocannabinoid biosynthesis4
包装
1 g in glass bottle

详细说明 (English)

Application
A key intermediate in prostaglandin synthesis.
Reactant for:
• Beirut reaction for the preparation of phosphonylated quinoxaline dioxides1
• Preparation of pyrrolomorphinan derivatives as κ opioid agonists via cyclocondensation, Vilsmeier-Haack formylation, Horner-Wadsworth-Emmons reaction, and Kocienski-modified Julia olefination from naltrexone methyl ether2
• Synthesis of C-glycosides amphiphiles via solvent-free Horner-Wadsworth-Emmons reaction with unprotected sugars3
• Preparation of specific inhibitors of endocannabinoid biosynthesis4
Packaging
1 g in glass bottle