CAS 915923-16-9
:2-amino-N-(4-ethylcyclohexyl)benzamide
Description:
2-amino-N-(4-ethylcyclohexyl)benzamide is an organic compound characterized by its amine and amide functional groups. It features a benzene ring substituted with an amino group and an N-alkyl side chain, specifically a 4-ethylcyclohexyl group, which contributes to its hydrophobic properties. The presence of the amino group suggests potential basicity and the ability to form hydrogen bonds, which can influence its solubility in various solvents. The compound's structure indicates it may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular interactions could be significant in drug design, particularly in targeting specific receptors or enzymes. Additionally, the cyclohexyl moiety may provide steric hindrance, affecting the compound's reactivity and binding affinity. Overall, 2-amino-N-(4-ethylcyclohexyl)benzamide presents a unique combination of functional groups that can lead to diverse chemical behavior and potential applications in medicinal chemistry.
Formula:C15H22N2O
InChI:InChI=1/C15H22N2O/c1-2-11-7-9-12(10-8-11)17-15(18)13-5-3-4-6-14(13)16/h3-6,11-12H,2,7-10,16H2,1H3,(H,17,18)
SMILES:CCC1CCC(CC1)N=C(c1ccccc1N)O
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