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Catalog Number:
04028
CAS Number:
20866-55-1
Ester de boc-L-tyrosine 4-nitrophényle
Purity:
≥ 99 % (CCM)
Synonym(s):
Boc-L-Tyr-ONp
Documents
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Informations sur le produit

Boc-L-tyrosine 4-nitrophenyl ester is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This derivative of tyrosine features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal choice for various applications in organic synthesis. Its unique structure allows for selective reactions, facilitating the incorporation of tyrosine into peptides and proteins, which are crucial in drug development and biochemistry.

In addition to its role in peptide synthesis, Boc-L-tyrosine 4-nitrophenyl ester serves as a valuable intermediate in the production of bioactive compounds and pharmaceuticals. Its ability to undergo further transformations while maintaining the integrity of the tyrosine moiety makes it a preferred choice among researchers and industry professionals. The compound's favorable properties, such as its high purity and reactivity, contribute to its effectiveness in developing novel therapeutics and conducting biochemical assays. Whether in academic research or industrial applications, Boc-L-tyrosine 4-nitrophenyl ester stands out as a reliable and efficient reagent for advancing scientific discovery.

Numéro CAS 
20866-55-1
Formule moléculaire
C20H22N2O7
Poids moléculaire 
402.4
Point de fusion 
146-155 °C
Rotation optique 
[a] D 24 = -5,5 ± 2º (C = 1 % dans l'acétone)
Informations générales
Numéro CAS 
20866-55-1
Formule moléculaire
C20H22N2O7
Poids moléculaire 
402.4
Point de fusion 
146-155 °C
Rotation optique 
[a] D 24 = -5,5 ± 2º (C = 1 % dans l'acétone)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
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Applications

Boc-L-tyrosine 4-nitrophenyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, particularly in the development of pharmaceuticals and biologically active compounds.
  • Drug Development: Its unique properties allow for the modification of drug candidates, enhancing their solubility and stability, which is essential in the formulation of effective medications.
  • Bioconjugation: The compound is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is vital in creating targeted therapies and diagnostic tools.
  • Research in Neuroscience: Due to its structural similarity to neurotransmitters, it is employed in studies exploring the role of tyrosine derivatives in brain function and neuropharmacology.
  • Fluorescent Labeling: Boc-L-tyrosine 4-nitrophenyl ester can be utilized in fluorescent labeling techniques, aiding in the visualization of biological samples in various research applications.

Citations