Ethyl (4-fluorobenzoyl)acetate,

Code: 146293-5G D2-231

Application

Reactant used as a precursor in: Condensation reactions with diamines via C-C bond cleavage for synthesis of benzimidazoles and perimidines for possible use as an...


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Your Price
€293.00 5G
€360.39 inc. VAT

Application

Reactant used as a precursor in: Condensation reactions with diamines via C-C bond cleavage for synthesis of benzimidazoles and perimidines for possible use as antimalarial treatments Base-promoted domino Michael addition / cyclization / elimination reactions for synthesis of hydroxybenzophenones Oxidative cross-coupling with indoles via dioxygen activation Cyclization of keto esters for synthesis of pyrones Lewis base catalyzed hydrosilylation for synthesis of α-acetoxy β-amino acid derivatives Conia-ene reactions for synthesis of methylenecyclopentane derivatives

General description

Ethyl (4-fluorobenzoyl)acetate on condensation with benzofurazan oxide yields 2-(carboethoxy)-3-(4′-fluoro)phenylquinoxaline1,4-dioxide.

Packaging

1, 5 g in glass bottle

bp117-120 °C (lit.)
density1.174 g/mL at 25 °C (lit.)
InChI keySJUXLKYJKQBZLM-UHFFFAOYSA-N
InChI1S/C11H11FO3/c1-2-15-11(14)7-10(13)8-3-5-9(12)6-4-8/h3-6H,2,7H2,1H3
Quality Level100
refractive indexn20/D 1.5040 (lit.)
SMILES stringCCOC(=O)CC(=O)c1ccc(F)cc1
Cas Number1999-00-4
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