(Z)-3-Phenyl-4-((phenylthio)methylene)isoxazol-5(4H)-one CAS 61861-81-2

Purity 97%+In StockPharmaceutical Standards
CAS No.61861-81-2
Molecular FormulaC16H11NO2S
Molecular Weight281.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(Z)-3-Phenyl-4-((phenylthio)methylene)isoxazol-5(4H)-one CAS 61861-81-2 chemical structure

Description

The molecular framework of (Z)-3-Phenyl-4-((phenylthio)methylene)isoxazol-5(4H)-one (C16H11NO2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies (Z)-3-Phenyl-4-((phenylthio)methylene)isoxazol-5(4H)-one (CAS 61861-81-2), a certified reference material (molecular formula C16H11NO2S, MW 281.33 g/mol) for analytical method development and quality control.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), (Z)-3-Phenyl-4-((phenylthio)methylene)isoxazol-5(4H)-one 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 FormulaC16H11NO2S
Molecular Weight281.33 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
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1974
Nitrogen Atoms1
Sulfur Atoms1

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