2-(3-(Trifluoromethyl)benzyl)-N-(3-(trifluoromethyl)phenyl)thiazole-4-carboxamide CAS 478042-41-0

Purity 97%+In StockPharmaceutical Standards
CAS No.478042-41-0
Molecular FormulaC19H12F6N2OS
Molecular Weight430.37 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(3-(Trifluoromethyl)benzyl)-N-(3-(trifluoromethyl)phenyl)thiazole-4-carboxamide CAS 478042-41-0 chemical structure

Description

2-(3-(Trifluoromethyl)benzyl)-N-(3-(trifluoromethyl)phenyl)thiazole-4-carboxamide (CAS 478042-41-0) is a high-purity analytical reference standard with the molecular formula C19H12F6N2OS and a molecular weight of 430.37 g/mol.

Based on its molecular formula C19H12F6N2OS, 2-(3-(Trifluoromethyl)benzyl)-N-(3-(trifluoromethyl)phenyl)thiazole-4-carboxamide contains a steroid core, 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 430.37 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 2-(3-(Trifluoromethyl)benzyl)-N-(3-(trifluoromethyl)phenyl)thiazole-4-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 FormulaC19H12F6N2OS
Molecular Weight430.37 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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