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Catalog Number:
07270
CAS Number:
127132-38-1
Boc -O -allyl-L-tyrosine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-L-Tyr(Tous)-OH
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$29.34 /1G
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Informations sur le produit

Boc-O-allyl-L-tyrosine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Its unique allyl substitution allows for selective reactions, facilitating the incorporation of this amino acid into various peptide sequences. This property is particularly beneficial in the design of targeted therapeutics and biologically active compounds.

In addition to its applications in peptide synthesis, Boc-O-allyl-L-tyrosine is also utilized in the development of novel materials and as a building block in organic synthesis. Its ability to undergo further functionalization opens up pathways for creating complex molecular architectures. Researchers appreciate its compatibility with various coupling reactions, which streamlines the synthesis process. With its favorable properties and broad applicability, Boc-O-allyl-L-tyrosine stands out as a valuable tool for advancing research and innovation in chemical and pharmaceutical industries.

Numéro CAS 
127132-38-1
Formule moléculaire
C 17 H 235
Poids moléculaire 
321.4
Rotation optique 
[a] D 20 = +17 ± 2º (C=1 dans MeOH)
Informations générales
Numéro CAS 
127132-38-1
Formule moléculaire
C 17 H 235
Poids moléculaire 
321.4
Rotation optique 
[a] D 20 = +17 ± 2º (C=1 dans MeOH)
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-allyl-L-tyrosine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of therapeutic proteins and vaccines, enhancing the efficiency of the process.
  • Drug Development: It plays a significant role in medicinal chemistry, where its unique structure aids in the design of novel drugs that target specific biological pathways, potentially leading to more effective treatments.
  • Bioconjugation: The compound is used in bioconjugation techniques, allowing researchers to attach biomolecules to drugs or imaging agents, improving the specificity and efficacy of therapies.
  • Research in Neuroscience: Its derivatives are explored in neuroscience research for their potential to modulate neurotransmitter activity, offering insights into neurological disorders.
  • Cosmetic Formulations: The compound is also being investigated for use in cosmetic products, where it may contribute to skin health and anti-aging formulations due to its antioxidant properties.

Citations