2-(4-Bromophenyl)-3-phenylthiazolidin-4-one CAS 128914-28-3

Purity 97%+In StockPharmaceutical Standards
CAS No.128914-28-3
Molecular FormulaC15H12BrNOS
Molecular Weight334.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-Bromophenyl)-3-phenylthiazolidin-4-one CAS 128914-28-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 334.23 g/mol gives 2-(4-Bromophenyl)-3-phenylthiazolidin-4-one distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 2-(4-Bromophenyl)-3-phenylthiazolidin-4-one (CAS 128914-28-3), a certified reference material (molecular formula C15H12BrNOS, MW 334.23 g/mol) for analytical method development and quality control.

The molecular framework of 2-(4-Bromophenyl)-3-phenylthiazolidin-4-one (C15H12BrNOS) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, bromine 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. 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.

CATO manufactures 2-(4-Bromophenyl)-3-phenylthiazolidin-4-one 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.

Physical & Chemical Properties

Molecular FormulaC15H12BrNOS
Molecular Weight334.23 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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