2-((3,4,4-Trifluorobut-3-en-1-yl)thio)-N-(4-(trifluoromethoxy)phenyl)nicotinamide CAS 478247-64-2

Purity 97%+In StockPharmaceutical Standards
CAS No.478247-64-2
Molecular FormulaC17H12F6N2O2S
Molecular Weight422.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((3,4,4-Trifluorobut-3-en-1-yl)thio)-N-(4-(trifluoromethoxy)phenyl)nicotinamide CAS 478247-64-2 chemical structure

Description

CATO supplies 2-((3,4,4-Trifluorobut-3-en-1-yl)thio)-N-(4-(trifluoromethoxy)phenyl)nicotinamide (CAS 478247-64-2), a certified reference material (molecular formula C17H12F6N2O2S, MW 422.34 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution, 2-((3,4,4-Trifluorobut-3-en-1-yl)thio)-N-(4-(trifluoromethoxy)phenyl)nicotinamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 422.34 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.

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-((3,4,4-Trifluorobut-3-en-1-yl)thio)-N-(4-(trifluoromethoxy)phenyl)nicotinamide 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 FormulaC17H12F6N2O2S
Molecular Weight422.34 g/mol
Purity97%+
StorageStore in a cool place (≤25°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.)2025
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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