N-(4-Methoxyphenyl)-2-{N-[3-(trifluoromethyl)phenyl]4-chlorobenzenesulfonamido}acetamide CAS 337922-19-7

Purity 97%+In StockPharmaceutical Standards
CAS No.337922-19-7
Molecular FormulaC22H18ClF3N2O4S
Molecular Weight498.90 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-Methoxyphenyl)-2-{N-[3-(trifluoromethyl)phenyl]4-chlorobenzenesulfonamido}acetamide CAS 337922-19-7 chemical structure

Description

As a certified reference material (CRM), N-(4-Methoxyphenyl)-2-{N-[3-(trifluoromethyl)phenyl]4-chlorobenzenesulfonamido}acetamide 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.

N-(4-Methoxyphenyl)-2-{N-[3-(trifluoromethyl)phenyl]4-chlorobenzenesulfonamido}acetamide (CAS 337922-19-7), molecular formula C22H18ClF3N2O4S and molecular weight 498.90 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of N-(4-Methoxyphenyl)-2-{N-[3-(trifluoromethyl)phenyl]4-chlorobenzenesulfonamido}acetamide (C22H18ClF3N2O4S) is characterized by a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC22H18ClF3N2O4S
Molecular Weight498.90 g/mol
Purity97%+
StorageStore in a cool place (≤25°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)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF/Cl-containing
Nitrogen Atoms2
Sulfur Atoms1

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