
CAS 654670-89-0
:Fmoc-Dap(Mtt)-OH
Description:
Fmoc-Dap(Mtt)-OH, also known as Fmoc-2,3-diaminopropionic acid (Mtt refers to a specific protecting group), is a chemical compound commonly used in peptide synthesis and research. It features a fluorenylmethyloxycarbonyl (Fmoc) group, which serves as a protective group for the amino functionality, allowing for selective reactions during peptide assembly. The presence of the Mtt (4-methyltrityl) group provides additional protection for the amino group, enhancing the stability of the compound during synthesis. This compound is typically utilized in solid-phase peptide synthesis, where it facilitates the formation of peptide bonds while preventing unwanted side reactions. Fmoc-Dap(Mtt)-OH is characterized by its ability to form stable amide bonds, making it valuable in the development of peptides with specific sequences and functionalities. Its solubility in organic solvents and compatibility with various coupling reagents further contribute to its utility in synthetic chemistry. Overall, Fmoc-Dap(Mtt)-OH is an important building block in the field of peptide chemistry, enabling the creation of complex peptide structures for research and therapeutic applications.
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Found 4 products.
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-[[(4-methylphenyl)diphenylmethyl]amino]-L-alanine
CAS:Formula:C38H34N2O4Purity:97%Color and Shape:SolidMolecular weight:582.6876Fmoc-Dap(Mtt)-OH
CAS:Controlled Product<p>Applications Fmoc-Dap(Mtt)-OH is used in the synthesis of cyclic peptides as inhibitors targeting substrate recruitment site of cyclin-dependent kinase complexes.<br>References Andrews, M., et al.: Org. Biomol. Chem., 2, 2735 (2004);<br></p>Formula:C38H34N2O4Color and Shape:NeatMolecular weight:582.7




