Benzyl (R)-3-fluoro-3-(hydroxymethyl)pyrrolidine-1-carboxylate is a chemical compound characterized by its pyrrolidine ring structure, which is a five-membered nitrogen-containing heterocycle. The presence of a fluorine atom at the 3-position of the pyrrolidine ring contributes to its unique reactivity and potential biological activity. The hydroxymethyl group also enhances its solubility and may influence its interaction with biological targets. As an ester, the carboxylate functional group indicates that it can undergo hydrolysis, making it relevant in various chemical reactions, including those in medicinal chemistry. The benzyl group attached to the carboxylate provides additional hydrophobic character, which can affect the compound's pharmacokinetics and binding affinity in biological systems. This compound may be of interest in drug development, particularly in the context of designing inhibitors or modulators of specific biological pathways. Its specific stereochemistry (R configuration) is crucial for its biological activity, as stereoisomers can exhibit significantly different effects in biological systems.

BENZYL (R)-3-FLUORO-3-(HYDROXYMETHYL)PYRROLIDINE-1-CARBOXYLATE

1893340-48-1: Benzyl (R)-3-fluoro-3-(hydroxymethyl)pyrrolidine-1-carboxylate is a chemical compound characterized by its pyrrolidine ring structure, which is a five-membered nitrogen-containing heterocycle. The presence of a fluorine atom at the 3-position of the pyrrolidine ring contributes to its unique reactivity and potential biological activity. The hydroxymethyl group also enhances its solubility and may influence its interaction with biological targets. As an ester, the carboxylate functional group indicates that it can undergo hydrolysis, making it relevant in various chemical reactions, including those in medicinal chemistry. The benzyl group attached to the carboxylate provides additional hydrophobic character, which can affect the compound's pharmacokinetics and binding affinity in biological systems. This compound may be of interest in drug development, particularly in the context of designing inhibitors or modulators of specific biological pathways. Its specific stereochemistry (R configuration) is crucial for its biological activity, as stereoisomers can exhibit significantly different effects in biological systems.

CAS 1893340-48-1

BENZYL (R)-3-FLUORO-3-(HYDROXYMETHYL)PYRROLIDINE-1-CARBOXYLATE

benzyl (3R)-3-fluoro-3-(hydroxymethyl)pyrrolidine-1-carboxylate

Ref: IN-DA01JU9B

BENZYL (R)-3-FLUORO-3-(HYDROXYMETHYL)PYRROLIDINE-1-CARBOXYLATE

Ref: 10-F537481