2-((4-Chlorobenzyl)sulfinyl)-N-(3-(trifluoromethyl)phenyl)acetamide CAS 339097-86-8

Purity 97%+In StockPharmaceutical Standards
CAS No.339097-86-8
Molecular FormulaC16H13ClF3NO2S
Molecular Weight375.79 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((4-Chlorobenzyl)sulfinyl)-N-(3-(trifluoromethyl)phenyl)acetamide CAS 339097-86-8 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 375.79 g/mol gives 2-((4-Chlorobenzyl)sulfinyl)-N-(3-(trifluoromethyl)phenyl)acetamide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

2-((4-Chlorobenzyl)sulfinyl)-N-(3-(trifluoromethyl)phenyl)acetamide (CAS 339097-86-8) is a high-purity analytical reference standard with the molecular formula C16H13ClF3NO2S and a molecular weight of 375.79 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution, 2-((4-Chlorobenzyl)sulfinyl)-N-(3-(trifluoromethyl)phenyl)acetamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 375.79 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

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 FormulaC16H13ClF3NO2S
Molecular Weight375.79 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF/Cl-containing
Nitrogen Atoms1
Sulfur Atoms1

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