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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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Product Information

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.

Synonyms
Boc-L-Tyr(Bzl)-OH
CAS Number
2130-96-3
Purity
99%
Molecular Formula
C21H25NO5
Molecular Weight
371.4
MDL Number
MFCD00065597
PubChem ID
294897
Optical Rotation
=+27°±1°(c=2% AcOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-L-Tyr(Bzl)-OH
CAS Number
2130-96-3
Purity
99%
Molecular Formula
C21H25NO5
Molecular Weight
371.4
MDL Number
MFCD00065597
PubChem ID
294897
Optical Rotation
=+27°±1°(c=2% AcOH)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
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