
Catalog Number	AR00VRCV
Chemical Name	N-alpha-(9-Fluorenylmethyloxycarbonyl)-L-methionyl-glycine
CAS Number	77275-43-5
Molecular Formula	C22H24N2O5S
Molecular Weight	428.5014
MDL Number	MFCD31380728
SMILES	CSCC[C@@H](C(=O)NCC(=O)O)NC(=O)OCC1c2ccccc2-c2c1cccc2

(S)-2-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(methylthio)butanamido)acetic acid, is a unique and versatile compound that finds significant application in chemical synthesis. This compound serves as a key building block in the creation of various peptide structures due to its specific chemical properties.In chemical synthesis, (S)-2-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(methylthio)butanamido)acetic acid is commonly employed as a chiral amino acid derivative. Its chiral nature enables it to impart stereochemistry and specificity to peptide chains being synthesized. This compound acts as a crucial component in the formation of peptide bonds, facilitating the creation of complex peptide structures with desired biological activities or functions.Moreover, owing to its structural features, this acid can also serve as a stabilizing agent for peptide assemblies and assist in the controlled assembly of peptide-based materials. Its precise chemical structure allows for selective interactions with other molecules during chemical reactions, enhancing the efficiency and accuracy of peptide synthesis processes.Overall, the application of (S)-2-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(methylthio)butanamido)acetic acid in chemical synthesis is instrumental in the production of tailored peptide compounds with specific functionalities, making it a valuable tool for researchers and chemists in the field of organic chemistry and biochemistry.