2-(4-Trifluoromethyl-phenyl)-thiazole-4-carboxylic acid ethyl ester CAS 175204-88-3

Purity 97%+In StockPharmaceutical Standards
CAS No.175204-88-3
Molecular FormulaC13H10F3NO2S
Molecular Weight301.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-Trifluoromethyl-phenyl)-thiazole-4-carboxylic acid ethyl ester CAS 175204-88-3 chemical structure

Description

As a certified reference material (CRM), 2-(4-Trifluoromethyl-phenyl)-thiazole-4-carboxylic acid ethyl ester 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.

2-(4-Trifluoromethyl-phenyl)-thiazole-4-carboxylic acid ethyl ester (CAS 175204-88-3) is a high-purity analytical reference standard with the molecular formula C13H10F3NO2S and a molecular weight of 301.28 g/mol.

Based on its molecular formula C13H10F3NO2S, 2-(4-Trifluoromethyl-phenyl)-thiazole-4-carboxylic acid ethyl ester contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 301.28 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 FormulaC13H10F3NO2S
Molecular Weight301.28 g/mol
Purity97%+
StorageStore at 2-8°C, 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2007
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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