2-(4-Chlorophenyl)-N-(thiazol-2-yl)-2H-tetrazole-5-carboxamide CAS 1396792-16-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1396792-16-7
Molecular FormulaC11H7ClN6OS
Molecular Weight306.73 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-Chlorophenyl)-N-(thiazol-2-yl)-2H-tetrazole-5-carboxamide CAS 1396792-16-7 chemical structure

Description

CATO manufactures 2-(4-Chlorophenyl)-N-(thiazol-2-yl)-2H-tetrazole-5-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-(4-Chlorophenyl)-N-(thiazol-2-yl)-2H-tetrazole-5-carboxamide (CAS 1396792-16-7), a certified reference material (molecular formula C11H7ClN6OS, MW 306.73 g/mol) for analytical method development and quality control.

2-(4-Chlorophenyl)-N-(thiazol-2-yl)-2H-tetrazole-5-carboxamide (C11H7ClN6OS) contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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).

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 FormulaC11H7ClN6OS
Molecular Weight306.73 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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl-containing
Nitrogen Atoms6
Sulfur Atoms1

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