2-(4-Chlorophenyl)-3-(furan-2-ylmethyl)thiazolidin-4-one CAS 303226-46-2

Purity 97%+In StockPharmaceutical Standards
CAS No.303226-46-2
Molecular FormulaC14H12ClNO2S
Molecular Weight293.77 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-Chlorophenyl)-3-(furan-2-ylmethyl)thiazolidin-4-one CAS 303226-46-2 chemical structure

Description

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.

2-(4-Chlorophenyl)-3-(furan-2-ylmethyl)thiazolidin-4-one (CAS 303226-46-2) is a high-purity analytical reference standard with the molecular formula C14H12ClNO2S and a molecular weight of 293.77 g/mol.

Based on its molecular formula C14H12ClNO2S, 2-(4-Chlorophenyl)-3-(furan-2-ylmethyl)thiazolidin-4-one 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 293.77 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

As a certified reference material (CRM), 2-(4-Chlorophenyl)-3-(furan-2-ylmethyl)thiazolidin-4-one 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 FormulaC14H12ClNO2S
Molecular Weight293.77 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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