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Catalog Number:
05585
CAS Number:
103882-09-3
Boc-4-iodo-DL-phénylalanine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-DL-Phe(4-I)-OH, Boc - p-iodo-DL-Phe-OH, ( Acide RS -Boc-2-amino-3-(4-iodophényl)propionique
Documents
$58.39 /1G
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Product Information

Boc-4-iodo-DL-phenylalanine is a versatile amino acid derivative that plays a significant role in peptide synthesis and drug development. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and usability in various chemical reactions. Its unique structure, characterized by the presence of an iodine atom, allows for specific applications in medicinal chemistry, particularly in the design of novel therapeutics and radiolabeled compounds for imaging studies. Researchers appreciate its utility in the synthesis of peptides that require the introduction of iodine for biological activity or as a tracer in biological assays.

In addition to its applications in pharmaceutical research, Boc-4-iodo-DL-phenylalanine is also valuable in the study of protein interactions and enzyme mechanisms. Its ability to serve as a building block for more complex molecules makes it an essential tool for chemists and biochemists alike. By incorporating this compound into their research, professionals can explore new pathways in drug discovery and development, ultimately leading to innovative solutions in healthcare.

Synonyms
Boc-DL-Phe(4-I)-OH, Boc - p-iodo-DL-Phe-OH, ( Acide RS -Boc-2-amino-3-(4-iodophényl)propionique
CAS Number
103882-09-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C 14 H 18 INO 4
Molecular Weight
391.2
MDL Number
MFCD00176869
PubChem ID
3409757
Melting Point
163-169º C
Conditions
Conserver à 0-8°C
General Information
Synonyms
Boc-DL-Phe(4-I)-OH, Boc - p-iodo-DL-Phe-OH, ( Acide RS -Boc-2-amino-3-(4-iodophényl)propionique
CAS Number
103882-09-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C 14 H 18 INO 4
Molecular Weight
391.2
MDL Number
MFCD00176869
PubChem ID
3409757
Melting Point
163-169º C
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-4-iodo-DL-phenylalanine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those that require specific modifications for enhanced stability or activity.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for designing novel drugs, especially in targeting specific biological pathways.
  • Bioconjugation: The iodine atom in its structure allows for effective labeling and tracking in bioconjugation applications, aiding in the development of diagnostic tools.
  • Research in Neuroscience: It is used in studies related to neurotransmitter activity, helping researchers understand the role of amino acids in brain function.
  • Protein Engineering: The compound is instrumental in modifying proteins to enhance their functions, making it a vital tool in biotechnology and synthetic biology.

Citations