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Catalog Number:
12396
CAS Number:
204693-22-1
Fmoc-3,5-dibromo-D-tyrosine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-3,5-dibromo-D-tyr-OH
Documents
$58.39 /1G
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Product Information

Fmoc-3,5-dibromo-D-tyrosine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which facilitates the selective modification of the amino acid during solid-phase peptide synthesis. Its dibromo substitution enhances the compound's reactivity and allows for the introduction of additional functional groups, making it an excellent choice for researchers focusing on the development of novel peptides with enhanced biological activity.

In addition to its applications in peptide synthesis, Fmoc-3,5-dibromo-D-tyrosine is also valuable in the study of protein interactions and the design of biomaterials. Its structural properties enable the exploration of new therapeutic agents, particularly in the fields of oncology and neurobiology. Researchers appreciate its ability to provide insights into the mechanisms of action of various compounds, making it a critical tool in both academic and industrial laboratories.

Synonyms
Fmoc-3,5-dibromo-D-tyr-OH
CAS Number
204693-22-1
Purity
≥ 98% (HPLC)
Molecular Formula
C24H18NO5Br2
Molecular Weight
561.2
MDL Number
MFCD01076139
PubChem ID
18321117
Appearance
White powder
Optical Rotation
[a]D25 = - 7 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-3,5-dibromo-D-tyr-OH
CAS Number
204693-22-1
Purity
≥ 98% (HPLC)
Molecular Formula
C24H18NO5Br2
Molecular Weight
561.2
MDL Number
MFCD01076139
PubChem ID
18321117
Appearance
White powder
Optical Rotation
[a]D25 = - 7 ± 2º (C=1 in MeOH)
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

Fmoc-3,5-dibromo-D-tyrosine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing researchers to create complex peptide structures efficiently.
  • Drug Development: Its unique brominated structure enhances the pharmacological properties of peptides, making it valuable in the pharmaceutical industry for developing new therapeutic agents.
  • Bioconjugation: The chemical's functional groups facilitate bioconjugation processes, enabling the attachment of biomolecules to drugs or imaging agents, which is essential in targeted therapy and diagnostics.
  • Research in Neuroscience: It is used in studies related to neurotransmitter pathways, particularly due to its structural similarity to tyrosine, which is a precursor for important neurotransmitters.
  • Fluorescent Labeling: The fluorenyl group in this compound allows for fluorescent labeling, making it useful in various imaging techniques in biological research, enhancing visualization of cellular processes.

Citations