N,N-dimethyl-L-phenylalanine丨CAS 17469-89-5

N,N-dimethyl-L-phenylalanine丨CAS 17469-89-5
Product Introduction:
Catalog No.: SS131202
CAS No.: 17469-89-5
Purity(HPLC): 95% min
Product Name: N,N-dimethyl-L-phenylalanine
Molecular Formula: C11H15NO2
Molecular Weight: 193.24
Synonym(s): Alanine, N,N-dimethyl-3-phenyl-, L-
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Technical Parameters
Description

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Specifications

 

Appearance Off-white to white powder
Purity (HPLC) 95% min
Identification NMR (H)
Total impurity 5% max
Single impurity 3% max
Water content 0.5% max

 

 

 

Applications

 

N,N-Dimethyl-L-phenylalanine is primarily used as a chiral building block and intermediate in pharmaceutical and medicinal chemistry. It serves in the synthesis of peptide analogs, bioactive compounds, and modified amino acids for drug development. The compound's dimethylated amino group provides steric and electronic effects that are valuable in studying structure-activity relationships (SAR) and optimizing pharmacological properties of peptide-based therapeutics. It is also employed in research focused on enzyme inhibitors, receptor modulators, and other biologically active molecules.

 

Benefits

 

The key benefits of N,N-Dimethyl-L-phenylalanine include its enhanced chemical stability and its ability to impart steric hindrance and lipophilicity to peptide structures. The N,N-dimethyl modification can improve metabolic stability, membrane permeability, and bioavailability in pharmaceutical applications. Its chirality ensures enantioselective synthesis, which is critical for producing compounds with desired biological activity. Additionally, it provides synthetic flexibility, allowing for selective reactions at the amino and carboxyl sites for multi-step chemical transformations.

 

Conclusion

 

N,N-Dimethyl-L-phenylalanine is a valuable intermediate for the synthesis of modified peptides, bioactive molecules, and pharmaceutical candidates. Its chemical stability, chirality, and functional versatility make it essential in medicinal chemistry research and drug development, supporting the creation of compounds with enhanced biological and pharmacological properties.

 

 

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