物质信息
ID:329998
名称和标识
IUPAC标准名
dimethyl (2-oxoheptyl)phosphonate
IUPAC传统名
dimethyl 2-oxoheptylphosphonate
别名
Dimethyl 2-oxoheptylphosphonate(2-Oxoheptyl)phosphonic acid dimethyl ester(2-氧代庚基)膦酸二甲酯Dimethyl (hexanoylmethyl)phosphonate
化合物性质
安全信息
个人保护装置
Eyeshields, Gloves, half-mask respirator (US), multi-purpose combination respirator cartridge (US)
德国WGK号
3
MSDS下载
产品相关信息
纯度
85%
级别
technical grade
线性分子式
CH3(CH2)4COCH2P(O)(OCH3)2
理化性质
密度
1.07 g/mL at 25 °C(lit.)
闪点
230 °F
110 °C
沸点
109 °C/0.4 mmHg(lit.)
折射率
n20/D 1.444(lit.)
描述信息
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
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
分子图谱
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参考文献
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