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AB47686

109425-55-0 | Fmoc-Orn(Boc)-OH

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% HPLC in stock $6.00 $4.00 -   +
5g 98% in stock $8.00 $5.00 -   +
10g 98% HPLC in stock $10.00 $7.00 -   +
25g 98% HPLC in stock $19.00 $14.00 -   +
100g 98% HPLC in stock $61.00 $43.00 -   +
500g 98% HPLC in stock $302.00 $211.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB47686
Chemical Name: Fmoc-Orn(Boc)-OH
CAS Number: 109425-55-0
Molecular Formula: C25H30N2O6
Molecular Weight: 454.5155
MDL Number: MFCD00065668
SMILES: O=C(N[C@H](C(=O)O)CCCNC(=O)OC(C)(C)C)OCC1c2ccccc2c2c1cccc2

 

Computed Properties
Complexity: 669  
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: 11  
XLogP3: 4.1  

 

 

Upstream Synthesis Route
  • Fmoc-Orn(Boc)-OH, or N-(9-fluorenylmethoxycarbonyl)-Ornithine(Boc)-OH, is a key building block in the field of chemical synthesis. This compound is commonly used for the solid-phase peptide synthesis (SPPS) of peptides and proteins due to its ability to protect the amino group of ornithine while allowing for selective deprotection and subsequent coupling reactions.In chemical synthesis, Fmoc-Orn(Boc)-OH serves as a versatile tool for the controlled assembly of peptide sequences with high purity and efficiency. The Fmoc (9-fluorenylmethyloxycarbonyl) protecting group shields the N-terminal amine of ornithine, preventing unwanted side reactions during peptide elongation. On the other hand, the Boc (tert-butoxycarbonyl) protecting group on the side chain of ornithine ensures its stability and compatibility with various coupling reagents and conditions.By strategically incorporating Fmoc-Orn(Boc)-OH into solid-phase peptide synthesis protocols, chemists can efficiently construct complex peptide structures with precise control over sequence, length, and functionality. This compound enables the synthesis of biologically active peptides, pharmaceuticals, and peptide-based materials with tailored properties for research and industrial applications.
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