CAS 1375472-82-4
:2,2,2-Trifluoroethyl N-4-oxazolylcarbamate
Description:
2,2,2-Trifluoroethyl N-4-oxazolylcarbamate is a chemical compound characterized by its unique structure, which includes a trifluoroethyl group and an oxazolyl moiety linked through a carbamate functional group. This compound is typically a white to off-white solid at room temperature and is known for its stability under standard conditions. It exhibits low solubility in water but may dissolve in organic solvents, making it useful in various chemical applications. The presence of trifluoromethyl groups often imparts distinctive electronic properties, enhancing its reactivity and potential as a building block in synthetic chemistry. Additionally, the oxazole ring contributes to its biological activity, which may include herbicidal or fungicidal properties, making it of interest in agricultural chemistry. Safety data should be consulted for handling and exposure risks, as fluorinated compounds can exhibit unique toxicological profiles. Overall, 2,2,2-Trifluoroethyl N-4-oxazolylcarbamate represents a versatile compound with applications in both research and industry.
Formula:C6H5F3N2O3
InChI:InChI=1S/C6H5F3N2O3/c7-6(8,9)2-14-5(12)11-4-1-13-3-10-4/h1,3H,2H2,(H,11,12)
InChI key:InChIKey=XHGFLJIRRDBAKL-UHFFFAOYSA-N
SMILES:N(C(OCC(F)(F)F)=O)C1=COC=N1
Synonyms:- Carbamic acid, N-4-oxazolyl-, 2,2,2-trifluoroethyl ester
- 2,2,2-Trifluoroethyl N-4-oxazolylcarbamate
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 1 products.
2,2,2-Trifluoroethyl N-(1,3-oxazol-4-yl)carbamate
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H5F3N2O3Purity:Min. 95%Molecular weight:210.11 g/mol
