4-Methyl-2-(pyridin-4-yl)-N-[4-(trifluoromethoxy)phenyl]-1,3-thiazole-5-carboxamide CAS 338396-94-4

Purity 97%+In StockPharmaceutical Standards
CAS No.338396-94-4
Molecular FormulaC17H12F3N3O2S
Molecular Weight379.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Methyl-2-(pyridin-4-yl)-N-[4-(trifluoromethoxy)phenyl]-1,3-thiazole-5-carboxamide CAS 338396-94-4 chemical structure

Description

As a certified reference material (CRM), 4-Methyl-2-(pyridin-4-yl)-N-[4-(trifluoromethoxy)phenyl]-1,3-thiazole-5-carboxamide meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

4-Methyl-2-(pyridin-4-yl)-N-[4-(trifluoromethoxy)phenyl]-1,3-thiazole-5-carboxamide (CAS 338396-94-4), molecular formula C17H12F3N3O2S and molecular weight 379.36 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 4-Methyl-2-(pyridin-4-yl)-N-[4-(trifluoromethoxy)phenyl]-1,3-thiazole-5-carboxamide (C17H12F3N3O2S) contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 12.0, corresponding to approximately 12 ring(s) or double-bond equivalent(s). With a molecular weight of 379.36 g/mol, it falls into the moderately-high-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

Physical & Chemical Properties

Molecular FormulaC17H12F3N3O2S
Molecular Weight379.36 g/mol
Purity97%+
StorageStore at 2-8°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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

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