3-(N-(4-fluorophenyl)-N-methylsulfamoyl)thiophene-2-carboxylic acid CAS 950270-33-4

Purity 97%+In StockPharmaceutical Standards
CAS No.950270-33-4
Molecular FormulaC12H10FNO4S2
Molecular Weight315.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(N-(4-fluorophenyl)-N-methylsulfamoyl)thiophene-2-carboxylic acid CAS 950270-33-4 chemical structure

Description

CATO supplies 3-(N-(4-fluorophenyl)-N-methylsulfamoyl)thiophene-2-carboxylic acid (CAS 950270-33-4), a certified reference material (molecular formula C12H10FNO4S2, MW 315.34 g/mol) for analytical method development and quality control.

3-(N-(4-fluorophenyl)-N-methylsulfamoyl)thiophene-2-carboxylic acid (C12H10FNO4S2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine 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. 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.

As a certified reference material (CRM), 3-(N-(4-fluorophenyl)-N-methylsulfamoyl)thiophene-2-carboxylic acid meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC12H10FNO4S2
Molecular Weight315.34 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms2

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