
Catalog Number	AR00HFVL
Chemical Name	Nalpha-Fmoc-Nepsilon-Azido-D-Lysine
CAS Number	1198791-53-5
Molecular Formula	C21H22N4O4
Molecular Weight	394.4238
MDL Number	MFCD18427293
SMILES	[N-]=[N+]=NCCCC[C@H](C(=O)O)NC(=O)OCC1c2ccccc2c2c1cccc2

6-Azido-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-norleucine is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. As a key building block in peptide chemistry, this compound plays a crucial role in the development of novel pharmaceuticals and bioactive molecules. Its azido functional group allows for efficient and selective conjugation reactions, making it particularly valuable in the field of bioconjugation and drug delivery.In peptide synthesis, 6-Azido-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-norleucine serves as a key starting material for the construction of peptide sequences with precise control over stereochemistry and side chain functionalities. Its fluorenylmethoxycarbonyl (Fmoc) protecting group enhances the stability and compatibility of the amino acid during solid-phase peptide synthesis, leading to high purity and yield of the desired peptide product.Furthermore, the azido group in this compound enables efficient bioorthogonal chemistry, allowing for specific labeling and modification of biomolecules in complex biological systems. This feature has opened up new opportunities in chemical biology and drug discovery, enabling researchers to probe biological processes with enhanced precision and selectivity.Overall, the application of 6-Azido-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-norleucine in chemical synthesis offers a powerful tool for the design and synthesis of peptides, bioconjugates, and pharmaceutical compounds with tailored properties and functions. Its versatility and reactivity make it an indispensable component in the toolkit of chemists and researchers working at the forefront of organic and medicinal chemistry.