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Catalog Number:
02739
CAS Number:
218769-47-2
Boc-O-benzyl-3,5-dibromo-L-tyrosine
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-3,5-dibromo-L-Tyr(OBzl)-OH
Documents
$43.87 /1G
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Product Information

Boc-O-benzyl-3,5-dibromo-L-tyrosine is a specialized amino acid derivative that plays a significant role in peptide synthesis and medicinal chemistry. This compound features a unique structure that incorporates both bromine substituents and a benzyl group, enhancing its reactivity and versatility in various chemical reactions. Its protective Boc (tert-butyloxycarbonyl) group allows for selective deprotection, making it an ideal choice for researchers focusing on the synthesis of complex peptides and pharmaceuticals.

This compound is particularly valuable in the development of targeted therapies and drug discovery, where it can be utilized to create novel peptide-based drugs with improved efficacy and specificity. Its unique properties enable researchers to explore new avenues in medicinal chemistry, including the design of inhibitors and modulators for various biological targets. With its robust profile, Boc-O-benzyl-3,5-dibromo-L-tyrosine stands out as a crucial building block for innovative research and applications in the pharmaceutical industry.

Synonyms
Boc-3,5-dibromo-L-Tyr(OBzl)-OH
CAS Number
218769-47-2
Purity
≥ 99% (HPLC)
Molecular Formula
C21H23Br2NO5
Molecular Weight
529.2
MDL Number
MFCD00076992
PubChem ID
138114175
Melting Point
143-149 °C
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-3,5-dibromo-L-Tyr(OBzl)-OH
CAS Number
218769-47-2
Purity
≥ 99% (HPLC)
Molecular Formula
C21H23Br2NO5
Molecular Weight
529.2
MDL Number
MFCD00076992
PubChem ID
138114175
Melting Point
143-149 °C
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-benzyl-3,5-dibromo-L-tyrosine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex molecules for drug development.
  • Bioconjugation: It is employed in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, enhancing the functionality of therapeutic agents.
  • Drug Design: The unique bromine substitutions provide specific reactivity, making it advantageous in designing new pharmaceuticals with targeted properties.
  • Research in Neuroscience: Its structural similarity to neurotransmitters allows for studies in neuropharmacology, aiding in the understanding of receptor interactions.
  • Fluorescent Labeling: This compound can be used in fluorescent labeling techniques, helping visualize biological processes in real-time during experiments.

Citations