CAS 1286263-90-8
:1,1-Dimethylethyl N-[trans-4-[(cyclohexylmethyl)amino]cyclohexyl]carbamate
Description:
1,1-Dimethylethyl N-[trans-4-[(cyclohexylmethyl)amino]cyclohexyl]carbamate, identified by its CAS number 1286263-90-8, is a chemical compound characterized by its complex structure, which includes a carbamate functional group. This substance features a tert-butyl group (1,1-dimethylethyl) attached to a nitrogen atom, which is further connected to a cyclohexylmethylamino group. The presence of cyclohexyl rings contributes to its hydrophobic characteristics, potentially influencing its solubility and interaction with biological membranes. The compound's structure suggests it may exhibit specific pharmacological properties, making it of interest in medicinal chemistry. Its stability and reactivity can be influenced by the steric hindrance provided by the bulky tert-butyl group. Additionally, the presence of the carbamate moiety may impart certain biological activities, such as enzyme inhibition or modulation of receptor interactions. Overall, this compound's unique structural features suggest potential applications in drug development and therapeutic research, although specific biological activities would require further investigation.
Formula:C18H34N2O2
InChI:InChI=1/C18H34N2O2/c1-18(2,3)22-17(21)20-16-11-9-15(10-12-16)19-13-14-7-5-4-6-8-14/h14-16,19H,4-13H2,1-3H3,(H,20,21)/t15-,16-
InChI key:InChIKey=IRDRDVLZZPOHHG-WKILWMFINA-N
SMILES:N(CC1CCCCC1)[C@H]2CC[C@H](NC(OC(C)(C)C)=O)CC2
Synonyms:- 1,1-Dimethylethyl N-[trans-4-[(cyclohexylmethyl)amino]cyclohexyl]carbamate
- Carbamic acid, N-[trans-4-[(cyclohexylmethyl)amino]cyclohexyl]-, 1,1-dimethylethyl ester
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