4-(4-(3,4-Dichlorophenyl)thiazol-2-yl)benzoic acid CAS 338407-84-4

Purity 97%+In StockPharmaceutical Standards
CAS No.338407-84-4
Molecular FormulaC16H9Cl2NO2S
Molecular Weight350.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(4-(3,4-Dichlorophenyl)thiazol-2-yl)benzoic acid CAS 338407-84-4 chemical structure

Description

CATO manufactures 4-(4-(3,4-Dichlorophenyl)thiazol-2-yl)benzoic 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.

4-(4-(3,4-Dichlorophenyl)thiazol-2-yl)benzoic acid (CAS 338407-84-4) is a high-purity analytical reference standard with the molecular formula C16H9Cl2NO2S and a molecular weight of 350.22 g/mol.

4-(4-(3,4-Dichlorophenyl)thiazol-2-yl)benzoic acid (C16H9Cl2NO2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC16H9Cl2NO2S
Molecular Weight350.22 g/mol
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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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