logo
Home  > Life Science  > Amino acids  > Amino acid derivatives  > Fmoc-L-Lys(Alloc)-OH

AB46179

146982-27-6 | Fmoc-L-Lys(Alloc)-OH

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $10.00 $7.00 -   +
5g 98% in stock $16.00 $11.00 -   +
10g 98% in stock $20.00 $14.00 -   +
25g 98% in stock $42.00 $29.00 -   +
100g 98% in stock $163.00 $114.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB46179
Chemical Name: Fmoc-L-Lys(Alloc)-OH
CAS Number: 146982-27-6
Molecular Formula: C25H28N2O6
Molecular Weight: 452.4996
MDL Number: MFCD00190872
SMILES: C=CCOC(=O)NCCCC[C@@H](C(=O)O)NC(=O)OCC1c2ccccc2c2c1cccc2

 

Computed Properties
Complexity: 662  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 33  
Hydrogen Bond Acceptor Count: 6  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 13  
XLogP3: 4.1  

 

 

Upstream Synthesis Route
  • The compound N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-L-lysine, is a versatile building block utilized in chemical synthesis for the creation of peptide-based materials. Specifically, this compound functions as a protected lysine derivative, providing a means to incorporate the amino acid lysine into peptide sequences with precise control over its reactivity. Its unique structure allows for selective deprotection and subsequent functionalization, enabling the synthesis of complex peptide structures with tailored properties and functionalities. In addition, the incorporation of the fluorenylmethoxycarbonyl (Fmoc) and allyloxycarbonyl (Alloc) protecting groups offers enhanced stability and strategic handling during peptide assembly processes. This compound plays a crucial role in the efficient and controlled synthesis of peptides for various applications in drug development, materials science, and biological research.
FEATURED PRODUCTS