3-(3-Chloro-4-fluorobenzenesulfonyl)-6-methoxy-2H-chromen-2-one CAS 866346-85-2

Purity 97%+In StockPharmaceutical Standards
CAS No.866346-85-2
Molecular FormulaC16H10ClFO5S
Molecular Weight368.76 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(3-Chloro-4-fluorobenzenesulfonyl)-6-methoxy-2H-chromen-2-one CAS 866346-85-2 chemical structure

Description

CATO manufactures 3-(3-Chloro-4-fluorobenzenesulfonyl)-6-methoxy-2H-chromen-2-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-(3-Chloro-4-fluorobenzenesulfonyl)-6-methoxy-2H-chromen-2-one (CAS 866346-85-2) is a high-purity analytical reference standard with the molecular formula C16H10ClFO5S and a molecular weight of 368.76 g/mol.

3-(3-Chloro-4-fluorobenzenesulfonyl)-6-methoxy-2H-chromen-2-one (C16H10ClFO5S) contains a flavonoid core, a sulfone group, a hydroxyl group, an ether linkage, fluorine/chlorine 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.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC16H10ClFO5S
Molecular Weight368.76 g/mol
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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF/Cl-containing
Sulfur Atoms1

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