Ethyl 5-(4-fluorophenyl)-2-(methylthio)thiazole-4-carboxylate CAS 1422175-48-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1422175-48-1
Molecular FormulaC13H12FNO2S2
Molecular Weight297.37 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 5-(4-fluorophenyl)-2-(methylthio)thiazole-4-carboxylate CAS 1422175-48-1 chemical structure

Description

CATO manufactures Ethyl 5-(4-fluorophenyl)-2-(methylthio)thiazole-4-carboxylate 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.

Ethyl 5-(4-fluorophenyl)-2-(methylthio)thiazole-4-carboxylate (CAS 1422175-48-1) is a high-purity analytical reference standard with the molecular formula C13H12FNO2S2 and a molecular weight of 297.37 g/mol.

The molecular framework of Ethyl 5-(4-fluorophenyl)-2-(methylthio)thiazole-4-carboxylate (C13H12FNO2S2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC13H12FNO2S2
Molecular Weight297.37 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
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.)1991
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms2

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