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Catalog Number:
15099
CAS Number:
478183-66-3
Boc-3-iodo-D-phenylalanine
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-D-Phe(3-I)-OH, Boc-3-iodo-D-Phe-OH, (R-Boc-2-amino-3-(3-bromophenyl)propionic acid
Documents
$96.34 /250MG
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Product Information

Boc-3-iodo-D-phenylalanine is a versatile amino acid derivative that plays a significant role in peptide synthesis and medicinal chemistry. This compound is particularly valued for its ability to introduce iodine into peptide structures, which can enhance the biological activity and stability of the resulting peptides. Its unique Boc (tert-butyloxycarbonyl) protecting group allows for selective deprotection, making it an excellent choice for researchers looking to synthesize complex peptides with precision.

In the pharmaceutical industry, Boc-3-iodo-D-phenylalanine is utilized in the development of novel therapeutics, especially in the design of peptide-based drugs targeting specific biological pathways. Its application extends to the field of bioconjugation, where it can be used to create targeted drug delivery systems. The compound's stability and reactivity make it a preferred choice for researchers aiming to explore new avenues in drug design and development, providing a reliable building block for innovative therapeutic solutions.

Synonyms
Boc-D-Phe(3-I)-OH, Boc-3-iodo-D-Phe-OH, (R-Boc-2-amino-3-(3-bromophenyl)propionic acid
CAS Number
478183-66-3
Purity
≥ 99% (HPLC)
Molecular Formula
C14H18INO4
Molecular Weight
391.2
MDL Number
MFCD03840394
PubChem ID
21851057
Melting Point
113-121 °C
Appearance
White powder
Optical Rotation
[α]D25 = -16 ± 1º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-D-Phe(3-I)-OH, Boc-3-iodo-D-Phe-OH, (R-Boc-2-amino-3-(3-bromophenyl)propionic acid
CAS Number
478183-66-3
Purity
≥ 99% (HPLC)
Molecular Formula
C14H18INO4
Molecular Weight
391.2
MDL Number
MFCD03840394
PubChem ID
21851057
Melting Point
113-121 °C
Appearance
White powder
Optical Rotation
[α]D25 = -16 ± 1º (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

Boc-3-iodo-D-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, enabling researchers to create complex molecules for drug development.
  • Drug Design: Its unique structure allows for the exploration of new therapeutic agents, particularly in targeting specific receptors in the body, enhancing the efficacy of pharmaceuticals.
  • Bioconjugation: The compound can be used in bioconjugation techniques, facilitating the attachment of drugs or imaging agents to biomolecules, which is crucial in developing targeted therapies.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, helping researchers understand the mechanisms of action for various neurological disorders.
  • Analytical Chemistry: Its distinct properties make it useful in analytical methods for detecting and quantifying amino acids, aiding in quality control processes in pharmaceutical manufacturing.

Citations