4-(Chloromethyl)-2-(4-methanesulfonylphenyl)-1,3-thiazole CAS 1258641-29-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1258641-29-0
Molecular FormulaC11H10ClNO2S2
Molecular Weight287.79 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(Chloromethyl)-2-(4-methanesulfonylphenyl)-1,3-thiazole CAS 1258641-29-0 chemical structure

Description

CATO supplies 4-(Chloromethyl)-2-(4-methanesulfonylphenyl)-1,3-thiazole (CAS 1258641-29-0), a certified reference material (molecular formula C11H10ClNO2S2, MW 287.79 g/mol) for analytical method development and quality control.

The molecular framework of 4-(Chloromethyl)-2-(4-methanesulfonylphenyl)-1,3-thiazole (C11H10ClNO2S2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), 4-(Chloromethyl)-2-(4-methanesulfonylphenyl)-1,3-thiazole 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 FormulaC11H10ClNO2S2
Molecular Weight287.79 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms2

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