N-(3,5-Dichlorophenyl)-2-{[3-(trifluoromethyl)phenyl]methyl}-1,3-thiazole-4-carboxamide CAS 478030-73-8

Purity 97%+In StockPharmaceutical Standards
CAS No.478030-73-8
Molecular FormulaC18H11Cl2F3N2OS
Molecular Weight431.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3,5-Dichlorophenyl)-2-{[3-(trifluoromethyl)phenyl]methyl}-1,3-thiazole-4-carboxamide CAS 478030-73-8 chemical structure

Description

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

CATO supplies N-(3,5-Dichlorophenyl)-2-{[3-(trifluoromethyl)phenyl]methyl}-1,3-thiazole-4-carboxamide (CAS 478030-73-8), a certified reference material (molecular formula C18H11Cl2F3N2OS, MW 431.26 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine/chlorine substitution, N-(3,5-Dichlorophenyl)-2-{[3-(trifluoromethyl)phenyl]methyl}-1,3-thiazole-4-carboxamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 431.26 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 FormulaC18H11Cl2F3N2OS
Molecular Weight431.26 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/Cl-containing
Nitrogen Atoms2
Sulfur Atoms1

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