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Catalog Number:
02686
CAS Number:
117142-26-4
Boc-3-(3'-pyridyl)-L-alanine
Purity:
≥ 99 % (dosage)
Synonym(s):
Boc-L-Ala(3'-pyridyl)-OH, Boc-β-(3'-pyridyl)-Ala-OH, Acide boc-(S)-2-amino-3-(3'-pyridyl)propanoïque
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$88.83 /1G
Taille
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Informations sur le produit

Boc-3-(3'-pyridyl)-L-alanine is a versatile amino acid derivative that plays a significant role in the synthesis of peptide-based pharmaceuticals and bioactive compounds. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers engaged in peptide synthesis and drug development. Its unique pyridine ring structure contributes to its ability to interact with various biological targets, thus opening avenues for applications in medicinal chemistry and biochemistry.

In addition to its utility in peptide synthesis, Boc-3-(3'-pyridyl)-L-alanine can serve as a building block for the development of novel ligands and inhibitors in drug discovery. Its favorable properties, such as enhanced lipophilicity and bioavailability, make it a valuable candidate for formulating new therapeutic agents. Researchers can leverage this compound in studies focused on enzyme inhibition, receptor binding, and other biochemical interactions, thereby advancing their projects with a reliable and effective tool.

Numéro CAS 
117142-26-4
Formule moléculaire
C13H18N2O4
Poids moléculaire 
266.3
Point de fusion 
135 - 138 °C (lit.)
Rotation optique 
[a] D 20 = 16 ± 3 °
Informations générales
Numéro CAS 
117142-26-4
Formule moléculaire
C13H18N2O4
Poids moléculaire 
266.3
Point de fusion 
135 - 138 °C (lit.)
Rotation optique 
[a] D 20 = 16 ± 3 °
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
-
Applications

Boc-3-(3'-pyridyl)-L-alanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those with specific biological activities. Its protective Boc group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: In pharmaceutical research, it is used to design and develop new drugs targeting neurological disorders, leveraging its pyridine moiety for improved receptor binding.
  • Bioconjugation: The compound facilitates the conjugation of biomolecules, such as proteins and antibodies, to enhance their stability and efficacy in therapeutic applications.
  • Research on Neurotransmitters: It plays a role in studying neurotransmitter systems, aiding researchers in understanding their mechanisms and potential therapeutic targets.
  • Analytical Chemistry: Used as a standard in analytical methods, it helps in the quantification of related compounds, ensuring accuracy in research findings.

Citations