CAS 201487-98-1

Carbamic acid, N-cyclohexyl-, 2,2,2-trifluoroethyl ester

Description:

Carbamic acid, N-cyclohexyl-, 2,2,2-trifluoroethyl ester is an organic compound characterized by its carbamate functional group, which is derived from carbamic acid. This substance features a cyclohexyl group, contributing to its hydrophobic properties, and a trifluoroethyl moiety, which imparts unique electronic and steric characteristics due to the presence of fluorine atoms. The trifluoroethyl group enhances the compound's lipophilicity and may influence its reactivity and interaction with biological systems. Typically, carbamates are known for their applications in agriculture as pesticides and herbicides, as well as in pharmaceuticals. The presence of the cyclohexyl group may also affect the compound's solubility and stability. Additionally, the trifluoromethyl group can enhance the compound's metabolic stability and alter its pharmacokinetic properties. Overall, this compound's structure suggests potential utility in various chemical applications, although specific safety and handling guidelines should be consulted due to the presence of fluorinated components.

Formula: C₉H₁₄F₃NO₂

InChI: InChI=1S/C9H14F3NO2/c10-9(11,12)6-15-8(14)13-7-4-2-1-3-5-7/h7H,1-6H2,(H,13,14)

InChI key: InChIKey=RBZWLYFELFNTOQ-UHFFFAOYSA-N

SMILES: N(C(OCC(F)(F)F)=O)C1CCCCC1

Synonyms:

• Carbamic acid, cyclohexyl-, 2,2,2-trifluoroethyl ester
• Carbamic acid, N-cyclohexyl-, 2,2,2-trifluoroethyl ester
• 2,2,2-Trifluoroethyl N-cyclohexylcarbamate

2,2,2-Trifluoroethyl N-cyclohexylcarbamate

CAS: 201487-98-1

2,2,2-Trifluoroethyl N-cyclohexylcarbamate is a research tool that has been shown to inhibit ion channels. It can be used for the study of protein interactions and receptor activation. This product is also a ligand and acts as an agonist of peptides. 2,2,2-Trifluoroethyl N-cyclohexylcarbamate has CAS number 201487-98-1.

Formula: C₉H₁₄F₃NO₂

Purity: Min. 95%

Molecular weight: 225.21 g/mol

Ref: 3D-BIA48798