4-(2,6-Dichloroanilino)-3-thiophenecarboxylic Acid Methyl Ester CAS 72888-20-1

Purity 97%+In StockPharmaceutical Standards
CAS No.72888-20-1
Molecular FormulaC12H9Cl2NO2S
Molecular Weight302.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(2,6-Dichloroanilino)-3-thiophenecarboxylic Acid Methyl Ester CAS 72888-20-1 chemical structure

Description

As a certified reference material (CRM), 4-(2,6-Dichloroanilino)-3-thiophenecarboxylic Acid Methyl Ester meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

CATO supplies 4-(2,6-Dichloroanilino)-3-thiophenecarboxylic Acid Methyl Ester (CAS 72888-20-1), a certified reference material (molecular formula C12H9Cl2NO2S, MW 302.18 g/mol) for analytical method development and quality control.

The molecular framework of 4-(2,6-Dichloroanilino)-3-thiophenecarboxylic Acid Methyl Ester (C12H9Cl2NO2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. 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. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 FormulaC12H9Cl2NO2S
Molecular Weight302.18 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1977
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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