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AB51435

103365-47-5 | (S)-N-Boc-3-amino-3-phenylpropanoic acid

Packsize Purity Availability Price Discounted Price    Quantity
1g 97% in stock $90.00 $63.00 -   +
5g 98% in stock $168.00 $118.00 -   +
25g 97% in stock $760.00 $532.00 -   +
100g 97% in stock $1,879.00 $1,316.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB51435
Chemical Name: (S)-N-Boc-3-amino-3-phenylpropanoic acid
CAS Number: 103365-47-5
Molecular Formula: C14H19NO4
Molecular Weight: 265.3050
MDL Number: MFCD01860892
SMILES: O=C(OC(C)(C)C)N[C@H](c1ccccc1)CC(=O)O

 

Computed Properties
Complexity: 316  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 19  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 6  
XLogP3: 2  

 

 

Upstream Synthesis Route
  • The (S)-N-Boc-3-Amino-3-phenylpropanoic acid is a versatile compound utilized in various chemical synthesis processes. One significant application of this compound is as a key intermediate in the synthesis of pharmaceuticals and complex organic molecules. Due to its unique structure and functional groups, (S)-N-Boc-3-Amino-3-phenylpropanoic acid serves as a valuable building block for the creation of diverse compounds with biological activity.In peptide synthesis, this compound can be employed as a chiral starting material to introduce specific stereochemistry into peptide chains. Its Boc (tert-butoxycarbonyl) protecting group allows for selective deprotection under mild conditions, enabling precise control over the reactions involved in peptide bond formation. Additionally, the amino and phenyl groups present in the molecule can participate in various bonding interactions, facilitating the creation of intricate peptide structures.Moreover, (S)-N-Boc-3-Amino-3-phenylpropanoic acid can be utilized in the synthesis of peptidomimetics and drug-like molecules. By incorporating this compound into the molecular design, chemists can explore new avenues for drug discovery and development by modulating the properties of the resulting compounds. Its versatile nature makes it a valuable tool for fine-tuning the biological activity and pharmacokinetic profile of potential drug candidates.Overall, the (S)-N-Boc-3-Amino-3-phenylpropanoic acid plays a crucial role in chemical synthesis, particularly in the preparation of complex molecules with therapeutic potential. Its strategic use in peptide and drug synthesis underscores its importance in the field of medicinal chemistry and organic synthesis.
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