Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
02514
Boc-O-2-bromo-Z-D-tyrosine 4-oxymethylphenylacetamidomethyl resin
Synonym(s):
Boc-D-Tyr(2-Br-Z)-PAM resin
Documents
$60.39 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

Boc-O-2-bromo-Z-D-tyrosine 4-oxymethylphenylacetamidomethyl is a specialized compound that plays a crucial role in peptide synthesis and medicinal chemistry. This compound, characterized by its unique structure, is particularly valuable for researchers focused on developing novel therapeutics. Its bromo and Boc (tert-butyloxycarbonyl) groups enhance its reactivity and stability, making it an ideal candidate for various chemical transformations.

In practical applications, Boc-O-2-bromo-Z-D-tyrosine is utilized in the synthesis of biologically active peptides, which can be pivotal in drug discovery and development. Its ability to facilitate the introduction of specific amino acid residues allows for the creation of tailored peptides that can target specific biological pathways. This compound is also advantageous in the field of bioconjugation, where it can be used to link peptides to other biomolecules, enhancing their therapeutic efficacy. Researchers and industry professionals will find this compound invaluable for advancing their projects in peptide-based drug development and related fields.

Synonyms
Boc-D-Tyr(2-Br-Z)-PAM resin
MDL Number
MFCD00801189
Substitution
0.3-0.8 meq/g
Mesh Size
100-200 mesh
Conditions
Store at 0-8°C
%DVB
1% DVB
General Information
Synonyms
Boc-D-Tyr(2-Br-Z)-PAM resin
MDL Number
MFCD00801189
Substitution
0.3-0.8 meq/g
Mesh Size
100-200 mesh
Conditions
Store at 0-8°C
%DVB
1% DVB
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-O-2-bromo-Z-D-tyrosine 4-oxymethylphenylacetamidomethyl is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in creating modified amino acids that enhance the stability and bioactivity of therapeutic peptides.
  • Drug Development: It plays a crucial role in medicinal chemistry for developing new drugs, especially in targeting specific receptors due to its unique structural properties that can improve binding affinity.
  • Bioconjugation: The compound is used in bioconjugation techniques, allowing researchers to attach biomolecules to drugs or imaging agents, enhancing their efficacy and specificity in targeted therapies.
  • Research in Neuroscience: This chemical is valuable in neuroscience research for studying the effects of modified tyrosine derivatives on neurotransmitter systems, potentially leading to new insights in neuropharmacology.
  • Diagnostic Applications: It can be utilized in the development of diagnostic tools, where its unique properties allow for the creation of more sensitive assays for detecting specific biomolecules in clinical samples.

Citations