Ethyl-[4-(2-hydroxy-ethylamino)-cyclohexyl]-carbamic acid tert-butyl ester, identified by its CAS number 1353988-74-5, is a chemical compound that features a cyclohexyl ring substituted with a hydroxyethylamino group and an ester functional group. This compound is characterized by its potential use in medicinal chemistry, particularly in the development of pharmaceuticals due to its structural properties that may influence biological activity. The presence of the carbamic acid moiety suggests that it may exhibit interactions with biological targets, potentially acting as an inhibitor or modulator in various biochemical pathways. The tert-butyl ester group enhances lipophilicity, which can improve the compound's absorption and distribution in biological systems. Additionally, the hydroxyethylamino group may contribute to solubility and reactivity, making it a versatile candidate for further chemical modifications. Overall, this compound's unique structure and functional groups position it as a subject of interest in drug design and development.

Ethyl-[4-(2-hydroxy-ethylaMino)-cyclohexyl]-carbaMic acid tert-butyl ester

1353988-74-5: Ethyl-[4-(2-hydroxy-ethylamino)-cyclohexyl]-carbamic acid tert-butyl ester, identified by its CAS number 1353988-74-5, is a chemical compound that features a cyclohexyl ring substituted with a hydroxyethylamino group and an ester functional group. This compound is characterized by its potential use in medicinal chemistry, particularly in the development of pharmaceuticals due to its structural properties that may influence biological activity. The presence of the carbamic acid moiety suggests that it may exhibit interactions with biological targets, potentially acting as an inhibitor or modulator in various biochemical pathways. The tert-butyl ester group enhances lipophilicity, which can improve the compound's absorption and distribution in biological systems. Additionally, the hydroxyethylamino group may contribute to solubility and reactivity, making it a versatile candidate for further chemical modifications. Overall, this compound's unique structure and functional groups position it as a subject of interest in drug design and development.

CAS 1353988-74-5

Ethyl-[4-(2-hydroxy-ethylaMino)-cyclohexyl]-carbaMic acid tert-butyl ester