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AE10880

1175973-95-1 | Fmoc-O-allyl-L-m-tyrosine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $37.00 $26.00 -   +
250mg 98% in stock $44.00 $31.00 -   +
5g 97% in stock $853.00 $597.00 -   +
10g 97% in stock $1,319.00 $923.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE10880
Chemical Name: Fmoc-O-allyl-L-m-tyrosine
CAS Number: 1175973-95-1
Molecular Formula: C27H25NO5
Molecular Weight: 443.4911
MDL Number: MFCD08061623
SMILES: C=CCOc1cccc(c1)C[C@@H](C(=O)O)NC(=O)OCC1c2ccccc2c2c1cccc2

 

Computed Properties
Complexity: 659  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 33  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 10  
XLogP3: 5.3  

 

 

Upstream Synthesis Route
  • (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-(allyloxy)phenyl)propanoic acid is a valuable compound utilized in chemical synthesis due to its versatile applications. One of the key uses of this compound is in the preparation of peptide-based molecules through solid-phase peptide synthesis (SPPS). In peptide synthesis, this compound acts as a crucial amino acid derivative that can be incorporated into peptide chains with high efficiency.Additionally, (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-(allyloxy)phenyl)propanoic acid is employed in the synthesis of bioactive peptides and pharmaceuticals due to its specific stereochemistry and structural properties. Its unique structure allows for precise control over the stereochemistry of the resulting peptides, making it a valuable tool in the development of new drug candidates.Furthermore, this compound plays a significant role in the synthesis of peptide mimetics and peptidomimetics, which are compounds designed to mimic the structure and function of peptides while possessing improved stability and bioavailability. By incorporating (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-(allyloxy)phenyl)propanoic acid into the backbone of these molecules, chemists can create novel compounds with enhanced biological activity and therapeutic potential.
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