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

Catalog Number:
03912
CAS Number:
201484-26-6
Fmoc-3,5-dibromo-L-tyrosine
Purity:
≥ 99% (TLC)
Synonym(s):
Fmoc-3,5-dibromo-L-Tyr-OH
Documents
$60.39 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

Fmoc-3,5-dibromo-L-tyrosine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued in the field of medicinal chemistry for its unique brominated phenolic structure, which enhances the biological activity of peptides. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide chains, making it an essential building block for researchers focused on developing novel therapeutics.

The compound's distinctive properties, such as its increased hydrophobicity and potential for enhanced receptor binding, make it an attractive choice for the synthesis of bioactive peptides. Fmoc-3,5-dibromo-L-tyrosine has been successfully utilized in the design of peptide-based drugs targeting various diseases, including cancer and neurodegenerative disorders. Its ability to improve the stability and efficacy of peptide formulations positions it as a valuable asset in pharmaceutical research and development.

Synonyms
Fmoc-3,5-dibromo-L-Tyr-OH
CAS Number
201484-26-6
Purity
≥ 99% (TLC)
Molecular Formula
C24H19Br2NO5
Molecular Weight
561.2
MDL Number
MFCD00065686
PubChem ID
18321117
Melting Point
184-193 ºC
Appearance
White cyrstals
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-3,5-dibromo-L-Tyr-OH
CAS Number
201484-26-6
Purity
≥ 99% (TLC)
Molecular Formula
C24H19Br2NO5
Molecular Weight
561.2
MDL Number
MFCD00065686
PubChem ID
18321117
Melting Point
184-193 ºC
Appearance
White cyrstals
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-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, particularly in solid-phase peptide synthesis, allowing for the incorporation of brominated tyrosine residues that can enhance the properties of the resulting peptides.
  • Drug Development: Its unique structure makes it valuable in the design of novel pharmaceuticals, especially in targeting specific biological pathways, which can lead to more effective treatments with fewer side effects.
  • Bioconjugation: The presence of bromine atoms allows for selective reactions in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other compounds, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: This compound can be used to study the effects of brominated amino acids on neurotransmitter activity, providing insights into neurological functions and potential therapeutic targets for neurodegenerative diseases.
  • Fluorescent Labeling: Fmoc-3,5-dibromo-L-tyrosine can be utilized in the development of fluorescent probes, enhancing imaging techniques in biological research and allowing for real-time monitoring of cellular processes.

Citations