3-Phenethyl-5-(pyridin-3-ylmethylene)-2-thioxothiazolidin-4-one CAS 670269-73-5

Purity 97%+In StockPharmaceutical Standards
CAS No.670269-73-5
Molecular FormulaC17H14N2OS2
Molecular Weight326.44 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Phenethyl-5-(pyridin-3-ylmethylene)-2-thioxothiazolidin-4-one CAS 670269-73-5 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 3-Phenethyl-5-(pyridin-3-ylmethylene)-2-thioxothiazolidin-4-one.

3-Phenethyl-5-(pyridin-3-ylmethylene)-2-thioxothiazolidin-4-one (CAS 670269-73-5), molecular formula C17H14N2OS2 and molecular weight 326.44 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C17H14N2OS2, 3-Phenethyl-5-(pyridin-3-ylmethylene)-2-thioxothiazolidin-4-one contains a steroid core, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 326.44 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 FormulaC17H14N2OS2
Molecular Weight326.44 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Nitrogen Atoms2
Sulfur Atoms2

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Why CATO?