4-(n-(4-((Difluoromethyl)thio)phenyl)sulfamoyl)benzoic acid CAS 327092-87-5

Purity 97%+In StockPharmaceutical Standards
CAS No.327092-87-5
Molecular FormulaC14H11F2NO4S2
Molecular Weight359.37 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(n-(4-((Difluoromethyl)thio)phenyl)sulfamoyl)benzoic acid CAS 327092-87-5 chemical structure

Description

CATO supplies 4-(n-(4-((Difluoromethyl)thio)phenyl)sulfamoyl)benzoic acid (CAS 327092-87-5), a certified reference material (molecular formula C14H11F2NO4S2, MW 359.37 g/mol) for analytical method development and quality control.

Structurally, 4-(n-(4-((Difluoromethyl)thio)phenyl)sulfamoyl)benzoic acid (C14H11F2NO4S2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 359.37 g/mol, it falls into the moderately-high-molecular-weight range. 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.

CATO manufactures 4-(n-(4-((Difluoromethyl)thio)phenyl)sulfamoyl)benzoic 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.

Physical & Chemical Properties

Molecular FormulaC14H11F2NO4S2
Molecular Weight359.37 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms2

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