2-Phenyl-4-(phenylamino)-7-thioxofuro[3,4-d]pyrimidin-5(7H)-one CAS 104824-50-2

Purity 97%+In StockPharmaceutical Standards
CAS No.104824-50-2
Molecular FormulaC18H11N3O2S
Molecular Weight333.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Phenyl-4-(phenylamino)-7-thioxofuro[3,4-d]pyrimidin-5(7H)-one CAS 104824-50-2 chemical structure

Description

CATO supplies 2-Phenyl-4-(phenylamino)-7-thioxofuro[3,4-d]pyrimidin-5(7H)-one (CAS 104824-50-2), a certified reference material (molecular formula C18H11N3O2S, MW 333.36 g/mol) for analytical method development and quality control.

The molecular framework of 2-Phenyl-4-(phenylamino)-7-thioxofuro[3,4-d]pyrimidin-5(7H)-one (C18H11N3O2S) is characterized by a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage. 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).

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-Phenyl-4-(phenylamino)-7-thioxofuro[3,4-d]pyrimidin-5(7H)-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 FormulaC18H11N3O2S
Molecular Weight333.36 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
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Nitrogen Atoms3
Sulfur Atoms1

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