3-Acetyl-2-(4-fluorophenyl)thiazolidine-4-carboxylic acid CAS 312714-09-3

Purity 97%+In StockPharmaceutical Standards
CAS No.312714-09-3
Molecular FormulaC12H12FNO3S
Molecular Weight269.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Acetyl-2-(4-fluorophenyl)thiazolidine-4-carboxylic acid CAS 312714-09-3 chemical structure

Description

CATO supplies 3-Acetyl-2-(4-fluorophenyl)thiazolidine-4-carboxylic acid (CAS 312714-09-3), a certified reference material (molecular formula C12H12FNO3S, MW 269.29 g/mol) for analytical method development and quality control.

Structurally, 3-Acetyl-2-(4-fluorophenyl)thiazolidine-4-carboxylic acid (C12H12FNO3S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 269.29 g/mol, it falls into the medium-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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), 3-Acetyl-2-(4-fluorophenyl)thiazolidine-4-carboxylic 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 FormulaC12H12FNO3S
Molecular Weight269.29 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, 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; Hygroscopic; reseal immediately after opening; 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.)2025
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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