5-(2-Chlorobenzamido)-3-methylthiophene-2-carboxylic acid CAS 926228-57-1

Purity 97%+In StockPharmaceutical Standards
CAS No.926228-57-1
Molecular FormulaC13H10ClNO3S
Molecular Weight295.74 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(2-Chlorobenzamido)-3-methylthiophene-2-carboxylic acid CAS 926228-57-1 chemical structure

Description

CATO manufactures 5-(2-Chlorobenzamido)-3-methylthiophene-2-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.

5-(2-Chlorobenzamido)-3-methylthiophene-2-carboxylic acid (CAS 926228-57-1), molecular formula C13H10ClNO3S and molecular weight 295.74 g/mol, is a CATO reference standard with documented purity and traceability.

5-(2-Chlorobenzamido)-3-methylthiophene-2-carboxylic acid (C13H10ClNO3S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. It is notably hygroscopic, 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. 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 FormulaC13H10ClNO3S
Molecular Weight295.74 g/mol
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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