3-(3-(4-Fluorophenyl)-5-methyl-7-oxo-7h-furo[3,2-g]chromen-6-yl)propanoic acid CAS 777857-50-8

Purity 97%+In StockPharmaceutical Standards
CAS No.777857-50-8
Molecular FormulaC21H15FO5
Molecular Weight366.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(3-(4-Fluorophenyl)-5-methyl-7-oxo-7h-furo[3,2-g]chromen-6-yl)propanoic acid CAS 777857-50-8 chemical structure

Description

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

CATO supplies 3-(3-(4-Fluorophenyl)-5-methyl-7-oxo-7h-furo[3,2-g]chromen-6-yl)propanoic acid (CAS 777857-50-8), a certified reference material (molecular formula C21H15FO5, MW 366.34 g/mol) for analytical method development and quality control.

3-(3-(4-Fluorophenyl)-5-methyl-7-oxo-7h-furo[3,2-g]chromen-6-yl)propanoic acid (C21H15FO5) contains a flavonoid core, a hydroxyl group, an ether linkage, fluorine substitution. Halogen substitution raises its density and boiling point, 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.

As a certified reference material (CRM), 3-(3-(4-Fluorophenyl)-5-methyl-7-oxo-7h-furo[3,2-g]chromen-6-yl)propanoic acid meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC21H15FO5
Molecular Weight366.34 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentF-containing

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