3-((4-Iodophenyl)sulfonyl)-2-phenylthiazolidine CAS 497234-88-5

Purity 97%+In StockPharmaceutical Standards
CAS No.497234-88-5
Molecular FormulaC15H14INO2S2
Molecular Weight431.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-((4-Iodophenyl)sulfonyl)-2-phenylthiazolidine CAS 497234-88-5 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 431.31 g/mol gives 3-((4-Iodophenyl)sulfonyl)-2-phenylthiazolidine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

3-((4-Iodophenyl)sulfonyl)-2-phenylthiazolidine (CAS 497234-88-5) is a high-purity analytical reference standard with the molecular formula C15H14INO2S2 and a molecular weight of 431.31 g/mol.

Based on its molecular formula C15H14INO2S2, 3-((4-Iodophenyl)sulfonyl)-2-phenylthiazolidine contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, iodine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 431.31 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC15H14INO2S2
Molecular Weight431.31 g/mol
Purity97%+
StorageStore at room temperature, 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; 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 ContentI-containing
Nitrogen Atoms1
Sulfur Atoms2

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