3-(2-Chlorophenyl)-7-hydroxy-2-(trifluoromethyl)-4h-chromen-4-one CAS 302953-05-5

Purity 97%+In StockPharmaceutical Standards
CAS No.302953-05-5
Molecular FormulaC16H8ClF3O3
Molecular Weight340.68 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(2-Chlorophenyl)-7-hydroxy-2-(trifluoromethyl)-4h-chromen-4-one CAS 302953-05-5 chemical structure

Description

CATO manufactures 3-(2-Chlorophenyl)-7-hydroxy-2-(trifluoromethyl)-4h-chromen-4-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.

3-(2-Chlorophenyl)-7-hydroxy-2-(trifluoromethyl)-4h-chromen-4-one (CAS 302953-05-5), molecular formula C16H8ClF3O3 and molecular weight 340.68 g/mol, is a CATO reference standard with documented purity and traceability.

3-(2-Chlorophenyl)-7-hydroxy-2-(trifluoromethyl)-4h-chromen-4-one (C16H8ClF3O3) contains a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution, a polycyclic aromatic system. 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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

Physical & Chemical Properties

Molecular FormulaC16H8ClF3O3
Molecular Weight340.68 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF/Cl-containing

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