4-(5-(3-Bromobenzylidene)-4-oxo-2-thioxothiazolidin-3-yl)butanoic acid CAS 303026-63-3

Purity 97%+In StockPharmaceutical Standards
CAS No.303026-63-3
Molecular FormulaC14H12BrNO3S2
Molecular Weight386.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(5-(3-Bromobenzylidene)-4-oxo-2-thioxothiazolidin-3-yl)butanoic acid CAS 303026-63-3 chemical structure

Description

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

4-(5-(3-Bromobenzylidene)-4-oxo-2-thioxothiazolidin-3-yl)butanoic acid (CAS 303026-63-3), molecular formula C14H12BrNO3S2 and molecular weight 386.28 g/mol, is a CATO reference standard with documented purity and traceability.

4-(5-(3-Bromobenzylidene)-4-oxo-2-thioxothiazolidin-3-yl)butanoic acid (C14H12BrNO3S2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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 FormulaC14H12BrNO3S2
Molecular Weight386.28 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms2

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