CAS 1087788-93-9
:2,2,2-Trifluoroethyl N-(2,5-difluorophenyl)carbamate
Description:
2,2,2-Trifluoroethyl N-(2,5-difluorophenyl)carbamate is a chemical compound characterized by its unique structure, which includes a trifluoroethyl group and a carbamate functional group. This compound is notable for its fluorinated moieties, which can enhance its lipophilicity and influence its biological activity. The presence of the difluorophenyl group suggests potential applications in pharmaceuticals or agrochemicals, as fluorinated compounds often exhibit improved metabolic stability and bioactivity. The carbamate functional group is known for its role in various chemical reactions and can serve as a protective group in organic synthesis. Additionally, the compound's molecular properties may contribute to its solubility and reactivity, making it of interest in both synthetic and applied chemistry. Safety and handling considerations are essential due to the presence of fluorine atoms, which can pose environmental and health risks. Overall, 2,2,2-Trifluoroethyl N-(2,5-difluorophenyl)carbamate exemplifies the significance of fluorinated compounds in modern chemistry.
Formula:C9H6F5NO2
InChI:InChI=1S/C9H6F5NO2/c10-5-1-2-6(11)7(3-5)15-8(16)17-4-9(12,13)14/h1-3H,4H2,(H,15,16)
InChI key:InChIKey=AQXFBDYYEBFVPS-UHFFFAOYSA-N
SMILES:N(C(OCC(F)(F)F)=O)C1=C(F)C=CC(F)=C1
Synonyms:- 2,2,2-Trifluoroethyl N-(2,5-difluorophenyl)carbamate
- Carbamic acid, N-(2,5-difluorophenyl)-, 2,2,2-trifluoroethyl ester
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Found 1 products.
2,2,2-Trifluoroethyl N-(2,5-difluorophenyl)carbamate
CAS:Versatile small molecule scaffoldFormula:C9H6F5NO2Purity:Min. 95%Molecular weight:255.14 g/mol
