2-Thioxo-3-(3-(trifluoromethyl)phenyl)-2,3-dihydroquinazolin-4(1h)-one CAS 81066-86-6

Purity 97%+In StockPharmaceutical Standards
CAS No.81066-86-6
Molecular FormulaC15H9F3N2OS
Molecular Weight322.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Thioxo-3-(3-(trifluoromethyl)phenyl)-2,3-dihydroquinazolin-4(1h)-one CAS 81066-86-6 chemical structure

Description

2-Thioxo-3-(3-(trifluoromethyl)phenyl)-2,3-dihydroquinazolin-4(1h)-one (C15H9F3N2OS) contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies 2-Thioxo-3-(3-(trifluoromethyl)phenyl)-2,3-dihydroquinazolin-4(1h)-one (CAS 81066-86-6), a certified reference material (molecular formula C15H9F3N2OS, MW 322.30 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-Thioxo-3-(3-(trifluoromethyl)phenyl)-2,3-dihydroquinazolin-4(1h)-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 FormulaC15H9F3N2OS
Molecular Weight322.30 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
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.)1980
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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