Z-D-Ala-Gly-OH, also known as Z-D-Alanine-Glycine, is a dipeptide derivative characterized by the presence of a Z (benzyloxycarbonyl) protecting group on the amino group of D-Alanine. This compound is typically used in peptide synthesis and research due to its structural properties that allow for the study of peptide interactions and biological activity. The Z group enhances the stability and solubility of the peptide, making it easier to handle in various chemical reactions. Z-D-Ala-Gly-OH is generally soluble in polar solvents, such as water and methanol, and exhibits typical peptide bond characteristics, including the ability to participate in hydrogen bonding and other interactions relevant to protein structure and function. Its CAS number, 34286-66-3, is a unique identifier that facilitates the identification and procurement of this compound in chemical databases and research settings. Overall, Z-D-Ala-Gly-OH serves as a valuable tool in the fields of biochemistry and medicinal chemistry for the synthesis of more complex peptide structures.

Z-D-Ala-Gly-OH

34286-66-3: Z-D-Ala-Gly-OH, also known as Z-D-Alanine-Glycine, is a dipeptide derivative characterized by the presence of a Z (benzyloxycarbonyl) protecting group on the amino group of D-Alanine. This compound is typically used in peptide synthesis and research due to its structural properties that allow for the study of peptide interactions and biological activity. The Z group enhances the stability and solubility of the peptide, making it easier to handle in various chemical reactions. Z-D-Ala-Gly-OH is generally soluble in polar solvents, such as water and methanol, and exhibits typical peptide bond characteristics, including the ability to participate in hydrogen bonding and other interactions relevant to protein structure and function. Its CAS number, 34286-66-3, is a unique identifier that facilitates the identification and procurement of this compound in chemical databases and research settings. Overall, Z-D-Ala-Gly-OH serves as a valuable tool in the fields of biochemistry and medicinal chemistry for the synthesis of more complex peptide structures.

CAS 34286-66-3

Z-D-Ala-Gly-OH

Z-D-Ala-Gly-OH

Ref: IN-DA007GVD

(R)-2-(2-(((Benzyloxy)carbonyl)amino)propanamido)acetic acid

Ref: 10-F324289