CAS 370-32-1
:2,2,2-trifluoroethyl phenylcarbamate
Description:
2,2,2-Trifluoroethyl phenylcarbamate, with the CAS number 370-32-1, is an organic compound characterized by its carbamate functional group, which is derived from the reaction of phenol and a trifluoroethyl isocyanate. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its stability under normal conditions, but it may decompose upon exposure to strong acids or bases. The presence of trifluoroethyl groups imparts unique properties, such as increased lipophilicity and potential bioactivity, making it of interest in various chemical applications, including agrochemicals and pharmaceuticals. Its molecular structure contributes to its reactivity, particularly in nucleophilic substitution reactions. Additionally, 2,2,2-trifluoroethyl phenylcarbamate may exhibit specific interactions with biological systems, which can be explored for potential therapeutic uses. However, safety precautions should be observed when handling this compound, as it may pose health risks if ingested or inhaled.
Formula:C9H8F3NO2
InChI:InChI=1/C9H8F3NO2/c10-9(11,12)6-15-8(14)13-7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14)
SMILES:c1ccc(cc1)N=C(O)OCC(F)(F)F
Synonyms:- Ethanol, 2,2,2-Trifluoro-, Phenylcarbamate
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Found 1 products.
2,2,2-Trifluoroethyl N-phenylcarbamate
CAS:Versatile small molecule scaffoldFormula:C9H8F3NO2Purity:Min. 95%Molecular weight:219.16 g/mol
