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Catalog Number:
16877
CAS Number:
1213571-65-3
Boc-O-Allyl-D-m-tyrosine
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-D-m-Tyr(All)-OH, Boc-D-3-Allyloxyphenylalanine
Documents
$105.00 /100MG
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Product Information

Boc-O-Allyl-D-m-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 reactivity, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Its unique structure allows for the incorporation of allyl and aromatic functionalities, facilitating the design of novel peptides with enhanced biological activity.

In practical applications, Boc-O-Allyl-D-m-tyrosine is utilized in the synthesis of bioactive peptides, which can serve as potential therapeutics in treating various diseases. Its ability to undergo selective reactions makes it a valuable building block for creating complex molecular architectures. Researchers appreciate its compatibility with various coupling methods, which streamlines the synthesis process. With its favorable properties and broad applicability, Boc-O-Allyl-D-m-tyrosine stands out as a key compound for advancing peptide-based research and development.

Synonyms
Boc-D-m-Tyr(All)-OH, Boc-D-3-Allyloxyphenylalanine
CAS Number
1213571-65-3
Purity
≥ 98% (HPLC)
Molecular Formula
C17H23NO5
Molecular Weight
321.37
MDL Number
MFCD08061616
PubChem ID
11163013
Appearance
Yellow oil
Optical Rotation
[a]D25 = - 24 ± 2 ° (C=1 in Ethanol)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-D-m-Tyr(All)-OH, Boc-D-3-Allyloxyphenylalanine
CAS Number
1213571-65-3
Purity
≥ 98% (HPLC)
Molecular Formula
C17H23NO5
Molecular Weight
321.37
MDL Number
MFCD08061616
PubChem ID
11163013
Appearance
Yellow oil
Optical Rotation
[a]D25 = - 24 ± 2 ° (C=1 in Ethanol)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-O-Allyl-D-m-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 novel therapeutic agents. Its unique structure allows for the incorporation of specific functionalities that enhance biological activity.
  • Drug Development: Researchers leverage its properties to create potential drug candidates, especially in the field of cancer therapy, where modifications to amino acids can lead to improved efficacy and reduced side effects.
  • Bioconjugation: The compound is utilized in bioconjugation processes, allowing for the attachment of drugs or imaging agents to proteins, which is essential in targeted drug delivery systems and diagnostic applications.
  • Research in Neuroscience: It plays a role in studies related to neurotransmitter systems, particularly in understanding the function of tyrosine derivatives in brain chemistry, which can lead to insights into neurological disorders.
  • Material Science: The compound is explored in the development of smart materials due to its ability to undergo chemical transformations, making it suitable for applications in responsive coatings and drug delivery systems.

Citations