(R)-Ethyl 2-amino-6-((tert-butoxycarbonyl)amino)hexanoate hydrochloride is a chiral amino acid derivative that serves as an important intermediate in the synthesis of peptides and pharmaceuticals. This compound features a hexanoate backbone with an ethyl ester group, which contributes to its solubility and reactivity. The presence of the tert-butoxycarbonyl (Boc) protecting group on the amino functionality allows for selective reactions, making it valuable in synthetic organic chemistry. As a hydrochloride salt, it is typically more stable and soluble in aqueous solutions, facilitating its use in biological and chemical applications. The compound's chirality, indicated by the (R) configuration, is crucial for its biological activity, as many biological processes are sensitive to the stereochemistry of amino acids. Overall, this substance is characterized by its utility in peptide synthesis, its stability as a hydrochloride salt, and its chiral nature, which is essential for its function in biological systems.

(R)-Ethyl 2-aMino-6-((tert-butoxycarbonyl)aMino)hexanoate hydrochloride

1313278-02-2: (R)-Ethyl 2-amino-6-((tert-butoxycarbonyl)amino)hexanoate hydrochloride is a chiral amino acid derivative that serves as an important intermediate in the synthesis of peptides and pharmaceuticals. This compound features a hexanoate backbone with an ethyl ester group, which contributes to its solubility and reactivity. The presence of the tert-butoxycarbonyl (Boc) protecting group on the amino functionality allows for selective reactions, making it valuable in synthetic organic chemistry. As a hydrochloride salt, it is typically more stable and soluble in aqueous solutions, facilitating its use in biological and chemical applications. The compound's chirality, indicated by the (R) configuration, is crucial for its biological activity, as many biological processes are sensitive to the stereochemistry of amino acids. Overall, this substance is characterized by its utility in peptide synthesis, its stability as a hydrochloride salt, and its chiral nature, which is essential for its function in biological systems.

CAS 1313278-02-2

(R)-Ethyl 2-aMino-6-((tert-butoxycarbonyl)aMino)hexanoate hydrochloride

(R)-Ethyl 2-amino-6-((tert-butoxycarbonyl)amino)hexanoate hydrochloride

Ref: IN-DA000VXI

Ethyl 6-N-Boc-D-lysinate hydrochloride

Ref: 10-F049990