N-(4-methoxyphenyl)-3-((3-(trifluoromethyl)benzyl)thio)thiophene-2-carboxamide CAS 250714-49-9

Purity 97%+In StockPharmaceutical Standards
CAS No.250714-49-9
Molecular FormulaC20H16F3NO2S2
Molecular Weight423.47 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-methoxyphenyl)-3-((3-(trifluoromethyl)benzyl)thio)thiophene-2-carboxamide CAS 250714-49-9 chemical structure

Description

CATO supplies N-(4-methoxyphenyl)-3-((3-(trifluoromethyl)benzyl)thio)thiophene-2-carboxamide (CAS 250714-49-9), a certified reference material (molecular formula C20H16F3NO2S2, MW 423.47 g/mol) for analytical method development and quality control.

The molecular framework of N-(4-methoxyphenyl)-3-((3-(trifluoromethyl)benzyl)thio)thiophene-2-carboxamide (C20H16F3NO2S2) 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).

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

CATO manufactures N-(4-methoxyphenyl)-3-((3-(trifluoromethyl)benzyl)thio)thiophene-2-carboxamide under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC20H16F3NO2S2
Molecular Weight423.47 g/mol
Purity97%+
StorageStore at room temperature, 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms2

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