5-Methyl-2-(pyridin-3-yl)thiazol-4-yl 3,4-dichlorobenzoate CAS 338398-96-2

Purity 97%+In StockPharmaceutical Standards
CAS No.338398-96-2
Molecular FormulaC16H10Cl2N2O2S
Molecular Weight365.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-Methyl-2-(pyridin-3-yl)thiazol-4-yl 3,4-dichlorobenzoate CAS 338398-96-2 chemical structure

Description

Based on its molecular formula C16H10Cl2N2O2S, 5-Methyl-2-(pyridin-3-yl)thiazol-4-yl 3,4-dichlorobenzoate contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 365.23 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

5-Methyl-2-(pyridin-3-yl)thiazol-4-yl 3,4-dichlorobenzoate (CAS 338398-96-2), molecular formula C16H10Cl2N2O2S and molecular weight 365.23 g/mol, is a CATO reference standard with documented purity and traceability.

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), 5-Methyl-2-(pyridin-3-yl)thiazol-4-yl 3,4-dichlorobenzoate 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 FormulaC16H10Cl2N2O2S
Molecular Weight365.23 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 ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

Related Methyl Standards

Recommended Standards

Why CATO?