6-Chloro-4,7-dimethyl-2-oxo-2H-chromene-3-carboxylic acid CAS 1361003-82-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1361003-82-8
Molecular FormulaC12H9ClO4
Molecular Weight252.65 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Chloro-4,7-dimethyl-2-oxo-2H-chromene-3-carboxylic acid CAS 1361003-82-8 chemical structure

Description

CATO manufactures 6-Chloro-4,7-dimethyl-2-oxo-2H-chromene-3-carboxylic acid 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.

CATO supplies 6-Chloro-4,7-dimethyl-2-oxo-2H-chromene-3-carboxylic acid (CAS 1361003-82-8), a certified reference material (molecular formula C12H9ClO4, MW 252.65 g/mol) for analytical method development and quality control.

The molecular framework of 6-Chloro-4,7-dimethyl-2-oxo-2H-chromene-3-carboxylic acid (C12H9ClO4) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 FormulaC12H9ClO4
Molecular Weight252.65 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, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl-containing

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