2-((2-(4-Fluorophenyl)-2-oxoethyl)thio)-3-phenylquinazolin-4(3H)-one CAS 292064-90-5

Purity 97%+In StockPharmaceutical Standards
CAS No.292064-90-5
Molecular FormulaC22H15FN2O2S
Molecular Weight390.43 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((2-(4-Fluorophenyl)-2-oxoethyl)thio)-3-phenylquinazolin-4(3H)-one CAS 292064-90-5 chemical structure

Description

Based on its molecular formula C22H15FN2O2S, 2-((2-(4-Fluorophenyl)-2-oxoethyl)thio)-3-phenylquinazolin-4(3H)-one contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 390.43 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO supplies 2-((2-(4-Fluorophenyl)-2-oxoethyl)thio)-3-phenylquinazolin-4(3H)-one (CAS 292064-90-5), a certified reference material (molecular formula C22H15FN2O2S, MW 390.43 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), 2-((2-(4-Fluorophenyl)-2-oxoethyl)thio)-3-phenylquinazolin-4(3H)-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 FormulaC22H15FN2O2S
Molecular Weight390.43 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
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)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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