1-(4-Fluorophenyl)-3-(furan-2-yl)-3-tosylpropan-1-one CAS 290839-61-1

Purity 97%+In StockPharmaceutical Standards
CAS No.290839-61-1
Molecular FormulaC20H17FO4S
Molecular Weight372.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-Fluorophenyl)-3-(furan-2-yl)-3-tosylpropan-1-one CAS 290839-61-1 chemical structure

Description

1-(4-Fluorophenyl)-3-(furan-2-yl)-3-tosylpropan-1-one (C20H17FO4S) contains a flavonoid core, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies 1-(4-Fluorophenyl)-3-(furan-2-yl)-3-tosylpropan-1-one (CAS 290839-61-1), a certified reference material (molecular formula C20H17FO4S, MW 372.41 g/mol) for analytical method development and quality control.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 1-(4-Fluorophenyl)-3-(furan-2-yl)-3-tosylpropan-1-one under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC20H17FO4S
Molecular Weight372.41 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Sulfur Atoms1

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