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Catalog Number:
07866
CAS Number:
138774-98-8
Boc- N -méthyl- O -benzyl-D-tyrosine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc- N -Me-D-Tyr(Bzl)-OH
Documents
$110.57 /250 mg
Taille
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Informations sur le produit

Boc-N-methyl-O-benzyl-D-tyrosine is a versatile amino acid derivative that plays a significant 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 working on complex peptide sequences. Its unique structure, characterized by the N-methyl and O-benzyl modifications, allows for improved selectivity and efficiency in various chemical reactions, particularly in the synthesis of biologically active peptides.

In pharmaceutical research, Boc-N-methyl-O-benzyl-D-tyrosine is utilized in the development of targeted therapies and drug candidates, especially in the fields of oncology and neurology. Its ability to serve as a building block for more complex structures enables researchers to explore new therapeutic avenues. Additionally, the compound's favorable properties, such as its compatibility with various coupling reagents, make it a valuable asset in the toolkit of synthetic chemists and biochemists alike, streamlining the process of peptide synthesis and enhancing the overall yield of desired products.

Numéro CAS 
138774-98-8
Formule moléculaire
C 22 H 275
Poids moléculaire 
385.46
Point de fusion 
127 - 129 ?C
Rotation optique 
[a] 20 D = 75 ± 1 ° (C=1 dans MeOH)
Informations générales
Numéro CAS 
138774-98-8
Formule moléculaire
C 22 H 275
Poids moléculaire 
385.46
Point de fusion 
127 - 129 ?C
Rotation optique 
[a] 20 D = 75 ± 1 ° (C=1 dans MeOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

Boc-N-methyl-O-benzyl-D-tyrosine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of therapeutic agents. Its protective groups allow for selective reactions, enhancing yield and purity.
  • Drug Development: Researchers leverage this compound in the design of novel drugs, especially in oncology and neurology, where modifications to amino acids can lead to improved efficacy and reduced side effects.
  • Bioconjugation: It is used in bioconjugation processes, allowing for the attachment of drugs or imaging agents to biomolecules, which is crucial in targeted therapy and diagnostics.
  • Research in Neuroscience: The compound's structural properties make it a candidate for studying neurotransmitter interactions, aiding in the understanding of various neurological disorders.
  • Custom Synthesis Services: Many chemical suppliers offer custom synthesis of this compound, catering to specific research needs, which provides flexibility and tailored solutions for scientists.

Citations