The chemical substance with the name "(2S)-2-(tert-butoxycarbonylamino)-4-hydroxy-butanoic acid; N,N-diethylethanamine" and CAS number 796072-25-8 is a compound that features both an amino acid structure and an amine component. It contains a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in organic synthesis to protect amine functionalities during chemical reactions. The presence of a hydroxy group indicates potential for hydrogen bonding and reactivity, while the butanoic acid moiety suggests it has acidic properties. The N,N-diethylethanamine part of the molecule introduces basic characteristics due to the presence of nitrogen atoms, which can participate in protonation and nucleophilic reactions. This compound may be utilized in peptide synthesis or as an intermediate in pharmaceutical development, given its structural features that allow for further functionalization. Its stereochemistry, indicated by the (2S) designation, suggests specific spatial arrangements that can influence biological activity and interactions. Overall, this compound exemplifies the complexity and versatility of organic molecules in medicinal chemistry.

(2S)-2-(tert-butoxycarbonylamino)-4-hydroxy-butanoic acid; N,N-diethylethanamine

796072-25-8: The chemical substance with the name "(2S)-2-(tert-butoxycarbonylamino)-4-hydroxy-butanoic acid; N,N-diethylethanamine" and CAS number 796072-25-8 is a compound that features both an amino acid structure and an amine component. It contains a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in organic synthesis to protect amine functionalities during chemical reactions. The presence of a hydroxy group indicates potential for hydrogen bonding and reactivity, while the butanoic acid moiety suggests it has acidic properties. The N,N-diethylethanamine part of the molecule introduces basic characteristics due to the presence of nitrogen atoms, which can participate in protonation and nucleophilic reactions. This compound may be utilized in peptide synthesis or as an intermediate in pharmaceutical development, given its structural features that allow for further functionalization. Its stereochemistry, indicated by the (2S) designation, suggests specific spatial arrangements that can influence biological activity and interactions. Overall, this compound exemplifies the complexity and versatility of organic molecules in medicinal chemistry.

CAS 796072-25-8

(2S)-2-(tert-butoxycarbonylamino)-4-hydroxy-butanoic acid; N,N-diethylethanamine

(S)-N-Boc-L-homoserine triethylammonium salt

Ref: 7W-GM8117