For research use only. Not for therapeutic Use.
N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N-allylglycine(Cat No.:I043024)is a modified glycine derivative where a fluorenylmethoxycarbonyl (Fmoc) group is attached to the amino group, and an allyl group is attached to the nitrogen atom. The Fmoc group serves as a protective group in peptide synthesis, preventing side reactions and allowing selective removal under basic conditions. The allyl group introduces a reactive functionality that can be used for further modifications or crosslinking. This compound is valuable in peptide synthesis, particularly in studies involving glycine residues and the design of functionalized peptides for research or therapeutic applications.
CAS Number | 222725-35-1 |
Synonyms | 2-[9H-fluoren-9-ylmethoxycarbonyl(prop-2-enyl)amino]acetic acid |
Molecular Formula | C20H19NO4 |
Purity | ≥95% |
IUPAC Name | 2-[9H-fluoren-9-ylmethoxycarbonyl(prop-2-enyl)amino]acetic acid |
InChI | InChI=1S/C20H19NO4/c1-2-11-21(12-19(22)23)20(24)25-13-18-16-9-5-3-7-14(16)15-8-4-6-10-17(15)18/h2-10,18H,1,11-13H2,(H,22,23) |
InChIKey | NVNQGCMKCQZFSM-UHFFFAOYSA-N |
SMILES | C=CCN(CC(=O)O)C(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13 |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |