7-Fluoro-4-hydroxycoumarin

• 产品号: 732982
• CAS号: 2145-27-9
• 分子式: C9H5FO3
• 分子量: 180.1326032

产品别名

• 标题: 7-Fluoro-4-hydroxycoumarin
• IUPAC标准名: 7-fluoro-4-hydroxy-2H-chromen-2-one
• IUPAC传统名: 7-fluoro-4-hydroxychromen-2-one
• 别名: 7-Fluoro-4-hydroxy-2H-chromen-2-one; 7-Fluoro-4-hydroxy-1(2H)-benzopyran-2-one

产品登记号

• MDL号: MFCD11845381
• CAS号: 2145-27-9

产品性质

• Empirical Formula (Hill Notation): C9H5FO3
• 熔点: 220-225 °C
• GHS警示词: Warning
• GHS危险声明: H302
• 欧盟危险性物质标志: 有害性(Harmful) (Xn)
• 危险公开号: 22
• 德国WGK号: 3

产品详细信息

详细说明 (English)

Packaging
250 mg in glass bottle
Application
Reactant for:
• Enantioselective synthesis of polycyclic coumarins via in situ formed primary amine-imine-catalyzed asymmetric Michael addition to cyclic enones1
• Preparation of dicoumarol analogs as inhibitors of human NAD(P)H quinone oxidoreductase-1 (NQO1) as agents active against human pancreatic and colon cancer cells2
• Imidazolidinecarboxylic acid-catalyzed asymmetric Michael reaction with unsaturated ketones in a highly atom-economic catalytic one-step formation of optically active warfarin anticoagulant3
• Asymmetric synthesis of functionalized α-keto esters and their hemiketal and hemiaminal derivatives via direct Michael addition with unsaturated α-keto esters catalyzed by bisoxazoline-copper(II) complexes4

详细说明 (简体中文)

包装
250 mg in glass bottle
Application
Reactant for:
• Enantioselective synthesis of polycyclic coumarins via in situ formed primary amine-imine-catalyzed asymmetric Michael addition to cyclic enones1
• Preparation of dicoumarol analogs as inhibitors of human NAD(P)H quinone oxidoreductase-1 (NQO1) as agents active against human pancreatic and colon cancer cells2
• Imidazolidinecarboxylic acid-catalyzed asymmetric Michael reaction with unsaturated ketones in a highly atom-economic catalytic one-step formation of optically active warfarin anticoagulant3
• Asymmetric synthesis of functionalized α-keto esters and their hemiketal and hemiaminal derivatives via direct Michael addition with unsaturated α-keto esters catalyzed by bisoxazoline-copper(II) complexes4