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Catalog Number:
15115
CAS Number:
244028-70-4
Fmoc-3-iodo-D-tyrosine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-m-iodo-D-Tyr-OH
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$65.40 /250MG
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Product Information

Fmoc-3-iodo-D-tyrosine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, characterized by the presence of iodine, enhances its reactivity and allows for the incorporation of iodine into peptides, which can be beneficial for various applications, including radiolabeling in imaging studies and the development of novel therapeutic agents.

Researchers and industry professionals appreciate Fmoc-3-iodo-D-tyrosine for its role in the synthesis of bioactive peptides and its potential in medicinal chemistry. Its ability to facilitate the introduction of iodine into peptide sequences opens up new avenues for the design of targeted therapies and diagnostic tools. The compound's stability and compatibility with standard peptide synthesis protocols make it an ideal choice for laboratories focused on peptide research and development.

Synonyms
Fmoc-m-iodo-D-Tyr-OH
CAS Number
244028-70-4
Purity
≥ 98% (HPLC)
Molecular Formula
C24H20NO5I
Molecular Weight
529.2
MDL Number
MFCD03840398
PubChem ID
53414213
Melting Point
147 - 157 ?C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = 10 ± 4 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-m-iodo-D-Tyr-OH
CAS Number
244028-70-4
Purity
≥ 98% (HPLC)
Molecular Formula
C24H20NO5I
Molecular Weight
529.2
MDL Number
MFCD03840398
PubChem ID
53414213
Melting Point
147 - 157 ?C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = 10 ± 4 º (C=1 in DMF)
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-iodo-D-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 custom sequences for various applications in drug development and biochemistry.
  • Bioconjugation: Its unique structure facilitates the attachment of biomolecules, making it valuable for creating targeted drug delivery systems and diagnostic tools in the pharmaceutical industry.
  • Fluorescent Probes: The incorporation of iodo groups enables the development of fluorescent probes for imaging applications, enhancing the visualization of cellular processes in research settings.
  • Antibody Production: Used in the design of immunogens, it aids in the generation of specific antibodies for research and therapeutic purposes, particularly in oncology and immunology.
  • Drug Design: The compound's properties allow for modifications that can improve the efficacy and selectivity of new drug candidates, addressing challenges in treating complex diseases.