n-(2-Chlorophenyl)-2-sulfanyl-1,3-benzoxazole-5-sulfonamide CAS 380426-70-0

Purity 97%+In StockPharmaceutical Standards
CAS No.380426-70-0
Molecular FormulaC13H9ClN2O3S2
Molecular Weight340.81 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-(2-Chlorophenyl)-2-sulfanyl-1,3-benzoxazole-5-sulfonamide CAS 380426-70-0 chemical structure

Description

CATO supplies n-(2-Chlorophenyl)-2-sulfanyl-1,3-benzoxazole-5-sulfonamide (CAS 380426-70-0), a certified reference material (molecular formula C13H9ClN2O3S2, MW 340.81 g/mol) for analytical method development and quality control.

n-(2-Chlorophenyl)-2-sulfanyl-1,3-benzoxazole-5-sulfonamide (C13H9ClN2O3S2) 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, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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-(2-Chlorophenyl)-2-sulfanyl-1,3-benzoxazole-5-sulfonamide 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 FormulaC13H9ClN2O3S2
Molecular Weight340.81 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms2

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