N-Phenyl-5-(trifluoromethyl)-1-benzothiophene-2-carboxamide CAS 439109-06-5

Purity 97%+In StockPharmaceutical Standards
CAS No.439109-06-5
Molecular FormulaC16H10F3NOS
Molecular Weight321.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-Phenyl-5-(trifluoromethyl)-1-benzothiophene-2-carboxamide CAS 439109-06-5 chemical structure

Description

Based on its molecular formula C16H10F3NOS, N-Phenyl-5-(trifluoromethyl)-1-benzothiophene-2-carboxamide contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 321.32 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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).

N-Phenyl-5-(trifluoromethyl)-1-benzothiophene-2-carboxamide (CAS 439109-06-5) is a high-purity analytical reference standard with the molecular formula C16H10F3NOS and a molecular weight of 321.32 g/mol.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

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 FormulaC16H10F3NOS
Molecular Weight321.32 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
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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