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AA94398

175453-07-3 | Fmoc-L-(3-pyridyl)alanine

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $7.00 $5.00 -   +
1g 98% in stock $10.00 $7.00 -   +
5g 98% in stock $46.00 $32.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA94398
Chemical Name: Fmoc-L-(3-pyridyl)alanine
CAS Number: 175453-07-3
Molecular Formula: C23H20N2O4
Molecular Weight: 388.4159
MDL Number: MFCD00144887
SMILES: O=C(N[C@H](C(=O)O)Cc1cccnc1)OCC1c2ccccc2c2c1cccc2

 

Computed Properties
Complexity: 561  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 29  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 7  
XLogP3: 3.6  

 

 

Upstream Synthesis Route
  • N-Fmoc-3-(3-pyridyl)-L-alanine, a versatile component commonly utilized in chemical synthesis, serves as a crucial building block in the creation of complex organic molecules. This compound plays a significant role in solid-phase peptide synthesis (SPPS), a method widely employed in the production of peptides with high purity and efficiency.N-Fmoc-3-(3-pyridyl)-L-alanine offers chemists the ability to selectively protect the amino group of the alanine residue during peptide synthesis, facilitating the stepwise assembly of peptide chains. Its Fmoc (9-fluorenylmethyloxycarbonyl) protective group can be easily removed under mild conditions, allowing for subsequent peptide chain elongation while minimizing side reactions and protecting the integrity of the peptide backbone.Furthermore, the 3-(3-pyridyl) functionality in N-Fmoc-3-(3-pyridyl)-L-alanine provides a unique handle for selective chemical modifications or conjugations, enabling tailored modifications to diversify the structure and properties of synthesized peptides. This compound's strategic placement within peptide sequences allows for the introduction of specific chemical functionalities or probes for various research and pharmaceutical applications.In summary, the strategic incorporation of N-Fmoc-3-(3-pyridyl)-L-alanine in chemical synthesis not only enhances the efficiency and precision of peptide assembly but also offers opportunities for further functionalization and customization, making it a valuable tool for scientists and researchers in the development of novel peptides and bioactive compounds.
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