4-Benzylaminocyclohexanone is an organic compound characterized by its cyclohexanone structure with a benzylamino group at the 4-position. It typically appears as a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. The compound features a ketone functional group, which contributes to its reactivity, particularly in nucleophilic addition reactions. Its molecular structure allows for potential interactions with biological systems, making it of interest in medicinal chemistry and drug development. The presence of the benzyl group can enhance lipophilicity, potentially influencing its pharmacokinetic properties. Additionally, 4-Benzylaminocyclohexanone may exhibit various physical properties such as solubility in organic solvents and moderate stability under standard conditions. Safety data should be consulted for handling, as compounds with amine and ketone functionalities can pose health risks. Overall, this compound's unique structure and functional groups make it a subject of interest in various chemical research fields.

4-Benzylaminocyclohexanone

142009-99-2: 4-(Benzylamino)Cyclohexanone Hcl, -Benzylaminocyclohexanone

Cyclohexanone, 4-[(phenylmethyl)amino]-

4-(Benzylamino)cyclohexanone is an ester of 4-benzyloxycarbonyloxycyclohexanone and formaldehyde. It is a radical cyclization enol ether that can be synthesized by reacting activated alkenes with trichloroacetamides. The synthesis of this compound involves the intramolecular transfer of an electron to form an intermediate radical, which reacts with a piperidine substituent to form the final product. This compound can also be synthesized synthetically by reacting an alkyne with ethyl nitrite in the presence of base.

CAS 142009-99-2: 4-Benzylaminocyclohexanone

Cyclohexanone, 4-[(phenylmethyl)amino]-

Ref: IN-DA001HJU

4-Benzylaminocyclohexanone

Ref: 10-F036890

4-(Benzylamino)cyclohexanone

Ref: 3D-FB51543