3-(3-Fluoro-4-methylphenyl)-2-mercaptoquinazolin-4(3H)-one CAS 1512-75-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1512-75-0
Molecular FormulaC15H11FN2OS
Molecular Weight286.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(3-Fluoro-4-methylphenyl)-2-mercaptoquinazolin-4(3H)-one CAS 1512-75-0 chemical structure

Description

The molecular framework of 3-(3-Fluoro-4-methylphenyl)-2-mercaptoquinazolin-4(3H)-one (C15H11FN2OS) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine substitution. 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies 3-(3-Fluoro-4-methylphenyl)-2-mercaptoquinazolin-4(3H)-one (CAS 1512-75-0), a certified reference material (molecular formula C15H11FN2OS, MW 286.32 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), 3-(3-Fluoro-4-methylphenyl)-2-mercaptoquinazolin-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 FormulaC15H11FN2OS
Molecular Weight286.32 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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