N-(4-(4-Chlorophenyl)thiazol-2-yl)-5-nitrothiophene-2-carboxamide CAS 324758-78-3

Purity 97%+In StockPharmaceutical Standards
CAS No.324758-78-3
Molecular FormulaC14H8ClN3O3S2
Molecular Weight365.81 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-(4-Chlorophenyl)thiazol-2-yl)-5-nitrothiophene-2-carboxamide CAS 324758-78-3 chemical structure

Description

Based on its molecular formula C14H8ClN3O3S2, N-(4-(4-Chlorophenyl)thiazol-2-yl)-5-nitrothiophene-2-carboxamide contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 365.81 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO supplies N-(4-(4-Chlorophenyl)thiazol-2-yl)-5-nitrothiophene-2-carboxamide (CAS 324758-78-3), a certified reference material (molecular formula C14H8ClN3O3S2, MW 365.81 g/mol) for analytical method development and quality control.

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.

CATO manufactures N-(4-(4-Chlorophenyl)thiazol-2-yl)-5-nitrothiophene-2-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.

Physical & Chemical Properties

Molecular FormulaC14H8ClN3O3S2
Molecular Weight365.81 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms2

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