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

Catalog Number:
15285
CAS Number:
269396-71-6
Boc-4-iodo-D-β-homophénylalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-D-β-HomoPhe(4-I)-OH, Acide boc-( R -3-amino-4-(4-iodophényl)butyrique
Documents
$93.14 /100 mg
Taille
Request Bulk Quote
Product Information

Boc-4-iodo-D-b-homophenylalanine is a valuable amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a unique Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for various synthetic applications. Its iodo substitution allows for further functionalization, enabling researchers to explore diverse chemical transformations and modifications.

In the field of medicinal chemistry, Boc-4-iodo-D-b-homophenylalanine serves as a crucial building block for the development of peptide-based therapeutics, particularly in the design of targeted drug delivery systems and biologically active peptides. Its ability to facilitate the introduction of iodine into peptide structures opens avenues for radiolabeling and imaging applications, enhancing the potential for diagnostic and therapeutic innovations. This compound's unique properties and versatility make it an essential tool for researchers aiming to advance their work in peptide chemistry and drug development.

Synonyms
Boc-D-β-HomoPhe(4-I)-OH, Acide boc-( R -3-amino-4-(4-iodophényl)butyrique
CAS Number
269396-71-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C 15 H 20 INO 4
Molecular Weight
405.23
MDL Number
MFCD01860963
PubChem ID
53397944
Melting Point
153-159 ?C
Appearance
Poudre blanche
Optical Rotation
[a] D 22 = +15 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-D-β-HomoPhe(4-I)-OH, Acide boc-( R -3-amino-4-(4-iodophényl)butyrique
CAS Number
269396-71-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C 15 H 20 INO 4
Molecular Weight
405.23
MDL Number
MFCD01860963
PubChem ID
53397944
Melting Point
153-159 ?C
Appearance
Poudre blanche
Optical Rotation
[a] D 22 = +15 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-4-iodo-D-b-homophenylalanine 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 peptides that can enhance biological activity.
  • Drug Development: Its unique structure allows for the design of novel pharmaceuticals, especially in targeting specific receptors or pathways in diseases, making it a key player in medicinal chemistry.
  • Bioconjugation: The presence of the iodine atom facilitates bioconjugation processes, enabling researchers to attach biomolecules for imaging or therapeutic purposes, which is crucial in biochemistry and molecular biology.
  • Research in Neuroscience: This compound can be utilized in studies related to neurotransmitter functions, providing insights into neurological disorders and potential treatments.
  • Material Science: Its properties can be exploited in the development of new materials, particularly in creating polymers or composites with specific functionalities, appealing to industries focused on advanced materials.

Citations