What is the Fmoc-Gly-Gly-OH?

Fmoc-Gly-Gly-OH is , while it's Molecular Formula is C19H18N2O5. Used in Peptide Synthesis: Fmoc-Gly-Gly-OH is used as a peptide linker for the synthesis of larger peptides and proteins. The Fmoc group provides a stable protecting group for the N-terminus, allowing for the stepwise addition of amino acids during solid-phase peptide synthesis. This method is widely employed in the production of therapeutic peptides, vaccines, and other bioactive molecules. Used in Drug Delivery Systems: In the pharmaceutical industry, Fmoc-Gly-Gly-OH is used as a component in the development of drug delivery systems. Its ability to form stable conjugates with various molecules, including drugs, targeting ligands, and imaging agents, makes it a valuable tool for enhancing the specificity, bioavailability, and overall efficacy of drug formulations. Used in Bioconjugation and Molecular Probes: Fmoc-Gly-Gly-OH is employed as a versatile building block in the creation of bioconjugates and molecular probes. Its reactivity and compatibility with various functional groups make it an ideal candidate for the development of novel imaging agents, biosensors, and other diagnostic tools. Used in Research and Development: In academic and industrial research settings, Fmoc-Gly-Gly-OH is used as a key component in the design and synthesis of novel bioactive molecules. Its ability to facilitate the formation of stable conjugates with a wide range of molecules makes it a valuable tool for exploring new chemical space and developing innovative therapeutic strategies. Used in Chemical Synthesis: Fmoc-Gly-Gly-OH is also utilized in various chemical synthesis processes, where its unique properties can be harnessed to create new compounds with potential applications in various industries, including pharmaceuticals, materials science, and agriculture.

What is the CAS number for Fmoc-Gly-Gly-OH?

The CAS number of Fmoc-Gly-Gly-OH is 35665-38-4.

What is Fmoc-Gly-Gly-OH (35665-38-4) used for?

Fmoc-Gly-Gly-OH is a peptide linker. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations.InChI:InChI=1/C19H18N2O5/c22-17(20-10-18(23)24)9-21-19(25)26-11-16-14-7-3-1-5-12(14)13-6-2-4-8-15(13)16/h1-8,16H,9-11H2,(H,20,22)(H,21,25)(H,23,24)