2-(3,4-Dichlorobenzoyl)-3-methyl-1-benzofuran CAS 400082-35-1

Purity 97%+In StockPharmaceutical Standards
CAS No.400082-35-1
Molecular FormulaC16H10Cl2O2
Molecular Weight305.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(3,4-Dichlorobenzoyl)-3-methyl-1-benzofuran CAS 400082-35-1 chemical structure

Description

CATO supplies 2-(3,4-Dichlorobenzoyl)-3-methyl-1-benzofuran (CAS 400082-35-1), a certified reference material (molecular formula C16H10Cl2O2, MW 305.16 g/mol) for analytical method development and quality control.

2-(3,4-Dichlorobenzoyl)-3-methyl-1-benzofuran (C16H10Cl2O2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, 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. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 2-(3,4-Dichlorobenzoyl)-3-methyl-1-benzofuran 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 FormulaC16H10Cl2O2
Molecular Weight305.16 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
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 ContentCl-containing

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