Tert-butyl 4-fluoro-3-(hydroxymethyl)piperidine-1-carboxylate is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The presence of a tert-butyl group contributes to its hydrophobic characteristics, while the 4-fluoro substituent introduces a polar functional group that can influence its reactivity and interaction with biological systems. The hydroxymethyl group at the 3-position adds a hydroxyl functional group, enhancing its potential for hydrogen bonding and solubility in polar solvents. As an ester, the carboxylate moiety indicates that it can undergo hydrolysis and other reactions typical of carboxylic acid derivatives. This compound may exhibit interesting pharmacological properties due to its structural features, making it a candidate for further research in medicinal chemistry. Its specific applications and behavior would depend on its interactions with biological targets, which could be influenced by the steric and electronic effects of its substituents.

tert-butyl 4-fluoro-3-(hydroxyMethyl)piperidine-1-carboxylate

1303972-97-5: Tert-butyl 4-fluoro-3-(hydroxymethyl)piperidine-1-carboxylate is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The presence of a tert-butyl group contributes to its hydrophobic characteristics, while the 4-fluoro substituent introduces a polar functional group that can influence its reactivity and interaction with biological systems. The hydroxymethyl group at the 3-position adds a hydroxyl functional group, enhancing its potential for hydrogen bonding and solubility in polar solvents. As an ester, the carboxylate moiety indicates that it can undergo hydrolysis and other reactions typical of carboxylic acid derivatives. This compound may exhibit interesting pharmacological properties due to its structural features, making it a candidate for further research in medicinal chemistry. Its specific applications and behavior would depend on its interactions with biological targets, which could be influenced by the steric and electronic effects of its substituents.

CAS 1303972-97-5

tert-butyl 4-fluoro-3-(hydroxyMethyl)piperidine-1-carboxylate

tert-Butyl 4-fluoro-3-(hydroxymethyl)piperidine-1-carboxylate

Ref: IN-DA000UCM

tert-Butyl 4-fluoro-3-(hydroxymethyl)piperidine-1-carboxylate

Ref: 54-PC430125