2-(2-((3-Chlorobenzyl)thio)thiazol-4-yl)acetic acid CAS 1050151-05-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1050151-05-7
Molecular FormulaC12H10ClNO2S2
Molecular Weight299.80 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(2-((3-Chlorobenzyl)thio)thiazol-4-yl)acetic acid CAS 1050151-05-7 chemical structure

Description

2-(2-((3-Chlorobenzyl)thio)thiazol-4-yl)acetic acid (C12H10ClNO2S2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 2-(2-((3-Chlorobenzyl)thio)thiazol-4-yl)acetic acid (CAS 1050151-05-7), a certified reference material (molecular formula C12H10ClNO2S2, MW 299.80 g/mol) for analytical method development and quality control.

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), 2-(2-((3-Chlorobenzyl)thio)thiazol-4-yl)acetic acid 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 FormulaC12H10ClNO2S2
Molecular Weight299.80 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.)1988
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms2

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