N-(2-((4-fluorobenzyl)thio)-2-methylpropyl)-4-methoxybenzenesulfonamide CAS 339104-23-3

Purity 97%+In StockPharmaceutical Standards
CAS No.339104-23-3
Molecular FormulaC18H22FNO3S2
Molecular Weight383.50 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(2-((4-fluorobenzyl)thio)-2-methylpropyl)-4-methoxybenzenesulfonamide CAS 339104-23-3 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO supplies N-(2-((4-fluorobenzyl)thio)-2-methylpropyl)-4-methoxybenzenesulfonamide (CAS 339104-23-3), a certified reference material (molecular formula C18H22FNO3S2, MW 383.50 g/mol) for analytical method development and quality control.

The molecular framework of N-(2-((4-fluorobenzyl)thio)-2-methylpropyl)-4-methoxybenzenesulfonamide (C18H22FNO3S2) is characterized by a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), 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).

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC18H22FNO3S2
Molecular Weight383.50 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; 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.)2025
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms2

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