(1-Tert-Butoxycarbonylamino-cyclohexyl)-acetic acid, identified by its CAS number 187610-56-6, is an organic compound characterized by the presence of a tert-butoxycarbonyl (Boc) protecting group attached to an amino group, which is further linked to a cyclohexyl moiety and an acetic acid functional group. This compound typically exhibits properties associated with amino acids, including potential solubility in polar solvents due to the presence of the carboxylic acid group. The Boc group serves as a protective group for the amino functionality, making it useful in peptide synthesis and organic synthesis applications. The cyclohexyl ring contributes to the compound's hydrophobic characteristics, influencing its overall solubility and reactivity. Additionally, the presence of both the amino and carboxylic acid functional groups allows for potential interactions such as hydrogen bonding, which can affect the compound's stability and reactivity in various chemical environments. Overall, this compound is of interest in medicinal chemistry and synthetic organic chemistry for its structural features and potential applications.

(1-TERT-BUTOXYCARBONYLAMINO-CYCLOHEXYL)-ACETIC ACID

187610-56-6: (1-Tert-Butoxycarbonylamino-cyclohexyl)-acetic acid, identified by its CAS number 187610-56-6, is an organic compound characterized by the presence of a tert-butoxycarbonyl (Boc) protecting group attached to an amino group, which is further linked to a cyclohexyl moiety and an acetic acid functional group. This compound typically exhibits properties associated with amino acids, including potential solubility in polar solvents due to the presence of the carboxylic acid group. The Boc group serves as a protective group for the amino functionality, making it useful in peptide synthesis and organic synthesis applications. The cyclohexyl ring contributes to the compound's hydrophobic characteristics, influencing its overall solubility and reactivity. Additionally, the presence of both the amino and carboxylic acid functional groups allows for potential interactions such as hydrogen bonding, which can affect the compound's stability and reactivity in various chemical environments. Overall, this compound is of interest in medicinal chemistry and synthetic organic chemistry for its structural features and potential applications.

CAS 187610-56-6

(1-TERT-BUTOXYCARBONYLAMINO-CYCLOHEXYL)-ACETIC ACID

(1-(tert-Butoxycarbonylamino)cyclohexyl)-acetic acid

Ref: IN-DA00AOOY

(1-Boc-aminocyclohexyl)acetic acid

Ref: 54-OR961369

2-(1-((tert-Butoxycarbonyl)amino)cyclohexyl)acetic acid

Ref: 10-F239807