5-(2-(Trifluoromethyl)phenyl)isoxazol-3-amine CAS 1498502-41-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1498502-41-2
Molecular FormulaC10H7F3N2O
Molecular Weight228.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(2-(Trifluoromethyl)phenyl)isoxazol-3-amine CAS 1498502-41-2 chemical structure

Description

5-(2-(Trifluoromethyl)phenyl)isoxazol-3-amine (C10H7F3N2O) contains a nitrogen-containing heterocyclic scaffold, an amide group, 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 5-(2-(Trifluoromethyl)phenyl)isoxazol-3-amine (CAS 1498502-41-2), a certified reference material (molecular formula C10H7F3N2O, MW 228.17 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), 5-(2-(Trifluoromethyl)phenyl)isoxazol-3-amine 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 FormulaC10H7F3N2O
Molecular Weight228.17 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentF-containing
Nitrogen Atoms2

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