2-{[4-(trifluoromethyl)phenyl]amino}-4H-3,1-benzoxazin-4-one CAS 278609-56-6

Purity 97%+In StockPharmaceutical Standards
CAS No.278609-56-6
Molecular FormulaC15H9F3N2O2
Molecular Weight306.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-{[4-(trifluoromethyl)phenyl]amino}-4H-3,1-benzoxazin-4-one CAS 278609-56-6 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

2-{[4-(trifluoromethyl)phenyl]amino}-4H-3,1-benzoxazin-4-one (CAS 278609-56-6), molecular formula C15H9F3N2O2 and molecular weight 306.24 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C15H9F3N2O2, 2-{[4-(trifluoromethyl)phenyl]amino}-4H-3,1-benzoxazin-4-one contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 306.24 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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).

CATO manufactures 2-{[4-(trifluoromethyl)phenyl]amino}-4H-3,1-benzoxazin-4-one under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC15H9F3N2O2
Molecular Weight306.24 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms2

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