(2Z)-3-(4-Fluorophenyl)-2-(nitromethylidene)-1,3-thiazolidin-4-one CAS 338417-49-5

Purity 97%+In StockPharmaceutical Standards
CAS No.338417-49-5
Molecular FormulaC10H7FN2O3S
Molecular Weight254.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(2Z)-3-(4-Fluorophenyl)-2-(nitromethylidene)-1,3-thiazolidin-4-one CAS 338417-49-5 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.

(2Z)-3-(4-Fluorophenyl)-2-(nitromethylidene)-1,3-thiazolidin-4-one (CAS 338417-49-5), molecular formula C10H7FN2O3S and molecular weight 254.24 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of (2Z)-3-(4-Fluorophenyl)-2-(nitromethylidene)-1,3-thiazolidin-4-one (C10H7FN2O3S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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).

CATO manufactures (2Z)-3-(4-Fluorophenyl)-2-(nitromethylidene)-1,3-thiazolidin-4-one under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC10H7FN2O3S
Molecular Weight254.24 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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