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Catalog Number:
15097
CAS Number:
261360-77-4
Boc-3-bromo-D-phenylalanine
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-D-Phe(3-Br)-OH, Boc-m-bromo-D-Phe-OH
Documents
$58.39 /1G
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Product Information

Boc-3-bromo-D-phenylalanine is a valuable amino acid derivative widely utilized in peptide synthesis and medicinal chemistry. This compound features a bromine atom on the phenyl ring, which enhances its reactivity and versatility in various chemical reactions. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective deprotection, making it an ideal choice for researchers looking to create complex peptide structures with precision.

This compound is particularly relevant in the development of pharmaceuticals, where it can serve as a building block for bioactive peptides. Its unique properties enable the synthesis of compounds with potential therapeutic applications, including those targeting neurological disorders and cancer. Researchers appreciate its stability and ease of handling, which facilitate efficient synthesis processes. Overall, Boc-3-bromo-D-phenylalanine stands out as a crucial tool for professionals in the fields of organic chemistry and drug development, offering significant advantages in the creation of innovative therapeutic agents.

Synonyms
Boc-D-Phe(3-Br)-OH, Boc-m-bromo-D-Phe-OH
CAS Number
261360-77-4
Purity
≥ 98% (HPLC)
Molecular Formula
C14H18BrNO4
Molecular Weight
344.2
MDL Number
MFCD01317704
PubChem ID
11695862
Appearance
Off-white solid
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-D-Phe(3-Br)-OH, Boc-m-bromo-D-Phe-OH
CAS Number
261360-77-4
Purity
≥ 98% (HPLC)
Molecular Formula
C14H18BrNO4
Molecular Weight
344.2
MDL Number
MFCD01317704
PubChem ID
11695862
Appearance
Off-white solid
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-3-bromo-D-phenylalanine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of biologically active compounds. Its protective Boc group allows for selective reactions, making it easier to manipulate during synthesis.
  • Drug Development: In pharmaceutical research, it is used to create novel drug candidates, especially in the field of cancer therapy. The incorporation of bromine can enhance the biological activity of the resulting compounds.
  • Bioconjugation: The unique structure of this amino acid derivative facilitates bioconjugation processes, allowing researchers to attach drugs or imaging agents to proteins, which is crucial in targeted therapy and diagnostics.
  • Research in Neuroscience: Its analogs are studied for their potential effects on neurotransmitter systems, providing insights into neurological disorders and paving the way for new treatment options.
  • Custom Synthesis: This compound is valuable in custom synthesis projects for academic and industrial labs, allowing for tailored solutions in research and development, particularly in medicinal chemistry.

Citations