N-(3-Chloro-2-quinoxalinyl)-4-fluorobenzenesulfonamide CAS 488744-02-1

Purity 97%+In StockPharmaceutical Standards
CAS No.488744-02-1
Molecular FormulaC14H9ClFN3O2S
Molecular Weight337.76 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-Chloro-2-quinoxalinyl)-4-fluorobenzenesulfonamide CAS 488744-02-1 chemical structure

Description

N-(3-Chloro-2-quinoxalinyl)-4-fluorobenzenesulfonamide (C14H9ClFN3O2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies N-(3-Chloro-2-quinoxalinyl)-4-fluorobenzenesulfonamide (CAS 488744-02-1), a certified reference material (molecular formula C14H9ClFN3O2S, MW 337.76 g/mol) for analytical method development and quality control.

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.

As a certified reference material (CRM), N-(3-Chloro-2-quinoxalinyl)-4-fluorobenzenesulfonamide 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 FormulaC14H9ClFN3O2S
Molecular Weight337.76 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.)2025
Halogen ContentF/Cl-containing
Nitrogen Atoms3
Sulfur Atoms1

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