2,5-Dichloro-N-(2-(methylthio)benzo[d]thiazol-6-yl)thiophene-3-carboxamide CAS 476643-30-8

Purity 97%+In StockPharmaceutical Standards
CAS No.476643-30-8
Molecular FormulaC13H8Cl2N2OS3
Molecular Weight375.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,5-Dichloro-N-(2-(methylthio)benzo[d]thiazol-6-yl)thiophene-3-carboxamide CAS 476643-30-8 chemical structure

Description

CATO manufactures 2,5-Dichloro-N-(2-(methylthio)benzo[d]thiazol-6-yl)thiophene-3-carboxamide 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 2,5-Dichloro-N-(2-(methylthio)benzo[d]thiazol-6-yl)thiophene-3-carboxamide (CAS 476643-30-8), a certified reference material (molecular formula C13H8Cl2N2OS3, MW 375.32 g/mol) for analytical method development and quality control.

The molecular framework of 2,5-Dichloro-N-(2-(methylthio)benzo[d]thiazol-6-yl)thiophene-3-carboxamide (C13H8Cl2N2OS3) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC13H8Cl2N2OS3
Molecular Weight375.32 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms3

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