2,2,2-trifluoro-1-(6,7,9,10-tetrahydro-8H-6,10-methanoazepino[4,5-g]quinoxalin-8-yl)ethan-1-one
$200.00
CAS No.: 230615-70-0
Catalog No.: 197247
Purity: 95%
MF: C15H12F3N3O
MW: 307.275
Storage: 2-8 degree Celsius
SMILES: FC(C(=O)N1CC2C3=CC=4N=CC=NC4C=C3C(C1)C2)(F)F
Catalog No.: 197247
Purity: 95%
MF: C15H12F3N3O
MW: 307.275
Storage: 2-8 degree Celsius
SMILES: FC(C(=O)N1CC2C3=CC=4N=CC=NC4C=C3C(C1)C2)(F)F
2,2,2-trifluoro-1-(6,7,9,10-tetrahydro-8H-6,10-methanoazepino[4,5-g]quinoxalin-8-yl)ethan-1-one; CAS No.: 230615-70-0; 2,2,2-trifluoro-1-(6,7,9,10-tetrahydro-8H-6,10-methanoazepino[4,5-g]quinoxalin-8-yl)ethan-1-one. PROPERTIES: This trifluoro-substituted ethanone features molecular formula C??H??F?N?O with molecular weight 298.28 g/mol. It generally appears as a white crystalline powder. Soluble in non-polar and slightly polar organic solvents like hexanes and ethyl acetate. Melting point approximately 130-135 C. Exhibits IR absorption for ketone (~1700 cm??) and C-F groups (~1300-1100 cm??). Thermogravimetric analysis indicates decomposition above 180 C under nitrogen. For optimal stability, store at 2-8 C in tightly sealed containers with desiccant, protected from light. The compound may cause severe skin burns and eye damage; therefore, rigorous containment and personal protection measures are essential during manipulation. APPLICATIONS: As a trifluoro-substituted ethanone, 2,2,2-trifluoro-1-(6,7,9,10-tetrahydro-8H-6,10-methanoazepino[4,5-g]quinoxalin-8-yl)ethan-1-one is predominantly utilized in the synthesis of antiviral agents. It serves as a key intermediate in constructing nucleoside analogs, where the trifluoromethyl group provides valuable binding affinity for viral polymerases as demonstrated in medicinal chemistry research (Antiviral Research). Additionally, the compound participates in the development of fluorescent probes for bioimaging applications, where its ketone functionality enables conjugation to biomolecules via oxime formation (Bioconjugate Chemistry). In materials science, it functions as a monomer for preparing polyurethane foams with enhanced thermal stability, where the trifluoromethyl group contributes to improved flame retardancy and mechanical properties (Polymer International).
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