(4S)-2-[2-(Trifluoromethoxy)phenyl]-1,3-thiazolidine-4-carboxylic acid CAS 1225071-50-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1225071-50-0
Molecular FormulaC11H10F3NO3S
Molecular Weight293.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(4S)-2-[2-(Trifluoromethoxy)phenyl]-1,3-thiazolidine-4-carboxylic acid CAS 1225071-50-0 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.

CATO supplies (4S)-2-[2-(Trifluoromethoxy)phenyl]-1,3-thiazolidine-4-carboxylic acid (CAS 1225071-50-0), a certified reference material (molecular formula C11H10F3NO3S, MW 293.26 g/mol) for analytical method development and quality control.

Based on its molecular formula C11H10F3NO3S, (4S)-2-[2-(Trifluoromethoxy)phenyl]-1,3-thiazolidine-4-carboxylic acid contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 293.26 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).

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 FormulaC11H10F3NO3S
Molecular Weight293.26 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 methanol, ethanol, 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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