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Catalog Number:
01390
CAS Number:
2130-96-3
Boc -O -benzyl-L-tyrosine
Purity:
99%
Synonym(s):
Boc-L-Tyr(Bzl)-OH
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Informations sur le produit

Boc-O-benzyl-L-tyrosine is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal choice for researchers working on complex peptide sequences. Its unique structure allows for selective reactions, facilitating the incorporation of tyrosine into peptides, which is crucial for developing biologically active compounds and therapeutic agents.

In addition to its applications in peptide synthesis, Boc-O-benzyl-L-tyrosine serves as a valuable building block in the design of enzyme inhibitors and drug candidates. Its ability to mimic natural amino acids while providing enhanced stability makes it particularly advantageous in medicinal chemistry. Researchers can leverage this compound to explore new therapeutic pathways, especially in the fields of oncology and neurology, where tyrosine derivatives play a significant role in drug development.

Numéro CAS 
2130-96-3
Formule moléculaire
C 21 H 255
Poids moléculaire 
371.4
Rotation optique 
=+27°±1°(c=2% AcOH)
Informations générales
Numéro CAS 
2130-96-3
Formule moléculaire
C 21 H 255
Poids moléculaire 
371.4
Rotation optique 
=+27°±1°(c=2% AcOH)
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 
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Applications

Boc-O-benzyl-L-tyrosine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids. Its stability under various conditions makes it a preferred choice for chemists.
  • Drug Development: In pharmaceutical research, it is used to create more effective drug candidates by modifying the structure of biologically active peptides, enhancing their efficacy and stability.
  • Bioconjugation: The compound can be employed in bioconjugation processes, linking biomolecules to therapeutic agents, which is crucial in developing targeted therapies in oncology and other fields.
  • Research in Neuroscience: It is used in studies involving neurotransmitter systems, particularly in the development of compounds that can influence dopamine pathways, which are vital in treating disorders like Parkinson's disease.
  • Material Science: The compound finds applications in creating functionalized polymers and materials, which can be used in drug delivery systems, enhancing the performance of medical devices.

Citations