2-((5-(n-(2-Chlorophenyl)sulfamoyl)benzo[d]oxazol-2-yl)thio)acetic acid CAS 750624-68-1

Purity 97%+In StockPharmaceutical Standards
CAS No.750624-68-1
Molecular FormulaC15H11ClN2O5S2
Molecular Weight398.84 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((5-(n-(2-Chlorophenyl)sulfamoyl)benzo[d]oxazol-2-yl)thio)acetic acid CAS 750624-68-1 chemical structure

Description

CATO manufactures 2-((5-(n-(2-Chlorophenyl)sulfamoyl)benzo[d]oxazol-2-yl)thio)acetic acid 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-(n-(2-Chlorophenyl)sulfamoyl)benzo[d]oxazol-2-yl)thio)acetic acid (CAS 750624-68-1), a certified reference material (molecular formula C15H11ClN2O5S2, MW 398.84 g/mol) for analytical method development and quality control.

2-((5-(n-(2-Chlorophenyl)sulfamoyl)benzo[d]oxazol-2-yl)thio)acetic acid (C15H11ClN2O5S2) contains a flavonoid core, 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC15H11ClN2O5S2
Molecular Weight398.84 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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms2

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