N-(4-Fluoro-3-nitrophenyl)-4-(trifluoromethyl)benzothioamide CAS 1257095-76-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1257095-76-3
Molecular FormulaC14H8F4N2O2S
Molecular Weight344.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-Fluoro-3-nitrophenyl)-4-(trifluoromethyl)benzothioamide CAS 1257095-76-3 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including N-(4-Fluoro-3-nitrophenyl)-4-(trifluoromethyl)benzothioamide.

CATO supplies N-(4-Fluoro-3-nitrophenyl)-4-(trifluoromethyl)benzothioamide (CAS 1257095-76-3), a certified reference material (molecular formula C14H8F4N2O2S, MW 344.28 g/mol) for analytical method development and quality control.

The molecular framework of N-(4-Fluoro-3-nitrophenyl)-4-(trifluoromethyl)benzothioamide (C14H8F4N2O2S) is characterized by a nitrogen-containing heterocyclic scaffold, 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 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).

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 FormulaC14H8F4N2O2S
Molecular Weight344.28 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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