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Catalog Number:
14786
CAS Number:
93267-04-0
Boc-β-iodo-Ala-OMe
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-β-iodo-L-Ala-OMe
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Product Information

Boc-b-iodo-Ala-OMe is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This amino acid derivative features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and reactivity, making it an ideal building block for the development of complex peptides and pharmaceuticals. Its unique structure, characterized by the presence of an iodine atom, allows for selective functionalization, providing researchers with the ability to introduce various modifications that can enhance biological activity or improve pharmacokinetic properties.

In the pharmaceutical industry, Boc-b-iodo-Ala-OMe is particularly valuable in the synthesis of peptide-based drugs, where precise control over the amino acid sequence is crucial. Its application extends to the development of targeted therapies and biologics, where the incorporation of iodine can facilitate imaging and tracking in biological systems. Researchers appreciate its ease of use and the efficiency it brings to synthetic pathways, making it a preferred choice for those looking to innovate in drug design and development.

Synonyms
Boc-β-iodo-L-Ala-OMe
CAS Number
93267-04-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 9 H 16 INO 4
Molecular Weight
329.14
MDL Number
MFCD00216579
PubChem ID
5051066
Melting Point
45 - 55 ?C
Appearance
Cristaux blancs à jaune clair
Optical Rotation
[a] D 20 = -4 ± 1 º (C = 2 dans MeOH)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Boc-β-iodo-L-Ala-OMe
CAS Number
93267-04-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 9 H 16 INO 4
Molecular Weight
329.14
MDL Number
MFCD00216579
PubChem ID
5051066
Melting Point
45 - 55 ?C
Appearance
Cristaux blancs à jaune clair
Optical Rotation
[a] D 20 = -4 ± 1 º (C = 2 dans MeOH)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-b-iodo-Ala-OMe is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of modified amino acids that enhance the stability and bioactivity of therapeutic peptides.
  • Drug Development: Its unique structure allows researchers to explore new drug candidates, especially in the field of oncology, where iodine-containing compounds can improve the targeting of cancer cells.
  • Bioconjugation: The presence of the iodo group facilitates bioconjugation reactions, enabling the attachment of biomolecules to surfaces or other compounds, which is crucial in creating targeted drug delivery systems.
  • Diagnostic Imaging: The iodine atom can be utilized in imaging techniques, such as PET scans, helping in the visualization of biological processes in real-time, which is essential for both research and clinical diagnostics.
  • Research in Chemical Biology: This compound is instrumental in studying protein interactions and modifications, providing insights into cellular mechanisms and potential therapeutic targets.

Citations