Identification | Back Directory | [Name]
7-Fluoro-4-hydroxy-2H-chromen-2-one | [CAS]
2145-27-9 | [Synonyms]
7-Fluoro-4-hydroxycoumarin 7-Fluoro-4-hydroxy-2H-chromen-2-one 7-Fluoro-4-hydroxy-2H-1-benzopyran-2-one 7-Fluoro-4-hydroxy-1(2H)-benzopyran-2-one 2H-1-Benzopyran-2-one, 7-fluoro-4-hydroxy- | [Molecular Formula]
C9H5FO3 | [MDL Number]
MFCD11845381 | [MOL File]
2145-27-9.mol | [Molecular Weight]
180.13 |
Hazard Information | Back Directory | [Uses]
Reactant for:
- Enantioselective synthesis of polycyclic coumarins via in situ formed primary amine-imine-catalyzed asymmetric Michael addition to cyclic enones
- Preparation of dicoumarol analogs as inhibitors of human NAD(P)H quinone oxidoreductase-1 (NQO1) as agents active against human pancreatic and colon cancer cells
- Imidazolidinecarboxylic acid-catalyzed asymmetric Michael reaction with unsaturated ketones in a highly atom-economic catalytic one-step formation of optically active warfarin anticoagulant
- 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) complexes
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