(Z)-5-(4-fluorobenzylidene)-3-(4-methylbenzyl)thiazolidine-2,4-dione CAS 870554-66-8

Purity 97%+In StockPharmaceutical Standards
CAS No.870554-66-8
Molecular FormulaC18H14FNO2S
Molecular Weight327.37 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(Z)-5-(4-fluorobenzylidene)-3-(4-methylbenzyl)thiazolidine-2,4-dione CAS 870554-66-8 chemical structure

Description

Structurally, (Z)-5-(4-fluorobenzylidene)-3-(4-methylbenzyl)thiazolidine-2,4-dione (C18H14FNO2S) contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 12.0, corresponding to approximately 12 ring(s) or double-bond equivalent(s). With a molecular weight of 327.37 g/mol, it falls into the moderately-high-molecular-weight range. 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 supplies (Z)-5-(4-fluorobenzylidene)-3-(4-methylbenzyl)thiazolidine-2,4-dione (CAS 870554-66-8), a certified reference material (molecular formula C18H14FNO2S, MW 327.37 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.

As a certified reference material (CRM), (Z)-5-(4-fluorobenzylidene)-3-(4-methylbenzyl)thiazolidine-2,4-dione meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC18H14FNO2S
Molecular Weight327.37 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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