(4s)-2-(2-(Trifluoromethoxy)phenyl)thiazolidine-4-carboxylic acid CAS 1103454-86-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1103454-86-9
Molecular FormulaC11H10F3NO3S
Molecular Weight293.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(4s)-2-(2-(Trifluoromethoxy)phenyl)thiazolidine-4-carboxylic acid CAS 1103454-86-9 chemical structure

Description

Based on its molecular formula C11H10F3NO3S, (4s)-2-(2-(Trifluoromethoxy)phenyl)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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO supplies (4s)-2-(2-(Trifluoromethoxy)phenyl)thiazolidine-4-carboxylic acid (CAS 1103454-86-9), a certified reference material (molecular formula C11H10F3NO3S, MW 293.26 g/mol) for analytical method development and quality control.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

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.)1989
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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