Ethyl 5-methyl-2-(pyridin-3-yl)thiazole-4-carboxylate CAS 39067-25-9

Purity 97%+In StockPharmaceutical Standards
CAS No.39067-25-9
Molecular FormulaC12H12N2O2S
Molecular Weight248.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 5-methyl-2-(pyridin-3-yl)thiazole-4-carboxylate CAS 39067-25-9 chemical structure

Description

CATO supplies Ethyl 5-methyl-2-(pyridin-3-yl)thiazole-4-carboxylate (CAS 39067-25-9), a certified reference material (molecular formula C12H12N2O2S, MW 248.30 g/mol) for analytical method development and quality control.

Ethyl 5-methyl-2-(pyridin-3-yl)thiazole-4-carboxylate (C12H12N2O2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage. It is notably hygroscopic, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

As a certified reference material (CRM), Ethyl 5-methyl-2-(pyridin-3-yl)thiazole-4-carboxylate 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.

Physical & Chemical Properties

Molecular FormulaC12H12N2O2S
Molecular Weight248.30 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
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1968
Nitrogen Atoms2
Sulfur Atoms1

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