N'-methyl-N'-(3-(trifluoromethyl)quinoxalin-2-yl)benzenesulfonohydrazide CAS 343372-58-7

Purity 97%+In StockPharmaceutical Standards
CAS No.343372-58-7
Molecular FormulaC16H13F3N4O2S
Molecular Weight382.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N'-methyl-N'-(3-(trifluoromethyl)quinoxalin-2-yl)benzenesulfonohydrazide CAS 343372-58-7 chemical structure

Description

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution, N'-methyl-N'-(3-(trifluoromethyl)quinoxalin-2-yl)benzenesulfonohydrazide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 382.36 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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).

CATO supplies N'-methyl-N'-(3-(trifluoromethyl)quinoxalin-2-yl)benzenesulfonohydrazide (CAS 343372-58-7), a certified reference material (molecular formula C16H13F3N4O2S, MW 382.36 g/mol) for analytical method development and quality control.

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 N'-methyl-N'-(3-(trifluoromethyl)quinoxalin-2-yl)benzenesulfonohydrazide 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 FormulaC16H13F3N4O2S
Molecular Weight382.36 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-containing
Nitrogen Atoms4
Sulfur Atoms1

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