Boc-Leu-Gly-OH, also known as Boc-Leucine-Glycine-OH, is a peptide derivative characterized by the presence of a tert-butyloxycarbonyl (Boc) protecting group on the leucine residue. This compound is typically utilized in peptide synthesis and research due to its role as a building block in the formation of larger peptides. The Boc group serves to protect the amino group during synthesis, allowing for selective reactions at other functional groups. The structure includes a leucine (Leu) and glycine (Gly) amino acid sequence, contributing to its properties as a dipeptide. It is generally soluble in organic solvents and exhibits stability under standard laboratory conditions. The compound's CAS number, 32991-17-6, is a unique identifier that facilitates its identification in chemical databases. In terms of applications, Boc-Leu-Gly-OH is often employed in the synthesis of more complex peptides and can be used in various biochemical studies, including those related to protein structure and function.

Boc-Leu-Gly-OH

32991-17-6: Boc-Leu-Gly-OH, also known as Boc-Leucine-Glycine-OH, is a peptide derivative characterized by the presence of a tert-butyloxycarbonyl (Boc) protecting group on the leucine residue. This compound is typically utilized in peptide synthesis and research due to its role as a building block in the formation of larger peptides. The Boc group serves to protect the amino group during synthesis, allowing for selective reactions at other functional groups. The structure includes a leucine (Leu) and glycine (Gly) amino acid sequence, contributing to its properties as a dipeptide. It is generally soluble in organic solvents and exhibits stability under standard laboratory conditions. The compound's CAS number, 32991-17-6, is a unique identifier that facilitates its identification in chemical databases. In terms of applications, Boc-Leu-Gly-OH is often employed in the synthesis of more complex peptides and can be used in various biochemical studies, including those related to protein structure and function.

CAS 32991-17-6

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