Tert-butyl (3R)-3-({[(benzyloxy)carbonyl]amino}methyl)pyrrolidine-1-carboxylate is a chemical compound characterized by its complex structure, which includes a pyrrolidine ring, a tert-butyl group, and a benzyloxycarbonyl amino group. This compound is typically classified as an amino acid derivative due to the presence of the carboxylate functional group. Its molecular structure contributes to its potential applications in medicinal chemistry, particularly in the synthesis of peptide-based drugs. The tert-butyl group enhances the compound's lipophilicity, which can influence its solubility and permeability in biological systems. The benzyloxycarbonyl moiety serves as a protective group for the amino functionality, making it useful in various synthetic pathways. Additionally, the stereochemistry at the 3-position of the pyrrolidine ring is significant, as it can affect the compound's biological activity and interaction with target proteins. Overall, this compound exemplifies the intricate design often found in pharmaceutical chemistry, where specific functional groups are strategically incorporated to achieve desired properties.

tert-butyl (3R)-3-({[(benzyloxy)carbonyl]amino}methyl)pyrrolidine-1-carboxylate

879275-54-4: Tert-butyl (3R)-3-({[(benzyloxy)carbonyl]amino}methyl)pyrrolidine-1-carboxylate is a chemical compound characterized by its complex structure, which includes a pyrrolidine ring, a tert-butyl group, and a benzyloxycarbonyl amino group. This compound is typically classified as an amino acid derivative due to the presence of the carboxylate functional group. Its molecular structure contributes to its potential applications in medicinal chemistry, particularly in the synthesis of peptide-based drugs. The tert-butyl group enhances the compound's lipophilicity, which can influence its solubility and permeability in biological systems. The benzyloxycarbonyl moiety serves as a protective group for the amino functionality, making it useful in various synthetic pathways. Additionally, the stereochemistry at the 3-position of the pyrrolidine ring is significant, as it can affect the compound's biological activity and interaction with target proteins. Overall, this compound exemplifies the intricate design often found in pharmaceutical chemistry, where specific functional groups are strategically incorporated to achieve desired properties.

CAS 879275-54-4

tert-butyl (3R)-3-({[(benzyloxy)carbonyl]amino}methyl)pyrrolidine-1-carboxylate

tert-Butyl (3R)-3-(([(benzyloxy)carbonyl]amino)methyl)pyrrolidine-1-carboxylate

Ref: IN-DA00ILC8

tert-butyl (3R)-3-({[(benzyloxy)carbonyl]amino}methyl)pyrrolidine-1-carboxylate

Ref: 10-F519130