甲氧甲酰基甲基三苯基溴化膦

• 产品号: 64939
• CAS号: 1779-58-4
• 分子式: C21H20BrO2P
• 分子量: 415.260061
• 纯 度: ≥97.0% (AT)

产品别名

• 标题: (Methoxycarbonylmethyl)triphenylphosphonium bromide
• IUPAC标准名: (2-methoxy-2-oxoethyl)triphenylphosphanium bromide
• IUPAC传统名: (2-methoxy-2-oxoethyl)triphenylphosphanium bromide
• 别名: (Carbomethoxymethyl)triphenylphosphonium bromide; NSC 136109; 羧甲氧基甲基三苯溴化磷

产品登记号

• EC号: 217-222-0
• MDL号: MFCD00011801
• Beilstein号: 3812975
• CAS号: 1779-58-4

产品性质

• 级别: purum
• 线性分子式: CH3OCOCH2P(Br)(C6H5)3
• 纯度: ≥97.0% (AT)
• 熔点: 165-170 °C (dec.)(lit.)
• GHS警示词: Warning
• GHS危险声明: H315-H319-H335
• 欧盟危险性物质标志: 刺激性(Irritant) (Xi)
• 个人保护装置: dust mask type N95 (US), Eyeshields, Gloves
• GHS警示性声明: P261-P305 + P351 + P338
• 危险公开号: 36/37/38
• 安全公开号: 26-36
• 保存温度: 2-8°C
• 德国WGK号: 3

产品详细信息

详细说明 (English)

Application
Reactant for synthesis of:
• GSK-3 inhibitors using theWittig reaction1
• Substituted furanones for antifungal and cytostatic activities2
• Photochromic dithienylethene derivatives3
• Gem-diiodoalkanes containing allylic alcohols4
• Highly substituted cyclopentenes and brazilanes via Au-catalyzed deoxygenative Nazarov cyclization5Reactant for:
• Asymmetric hydrogenation of α,β-unsaturated ester-phosphonates6
• Studies of thermal decomposition of phosphonium alkyl ester salts7

详细说明 (简体中文)

Application
Reactant for synthesis of:
• GSK-3 inhibitors using theWittig reaction1
• Substituted furanones for antifungal and cytostatic activities2
• Photochromic dithienylethene derivatives3
• Gem-diiodoalkanes containing allylic alcohols4
• Highly substituted cyclopentenes and brazilanes via Au-catalyzed deoxygenative Nazarov cyclization5Reactant for:
• Asymmetric hydrogenation of α,β-unsaturated ester-phosphonates6
• Studies of thermal decomposition of phosphonium alkyl ester salts7