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Catalog Number:
12797
CAS Number:
170848-34-7
Boc-3-iodo-D-alanine methyl ester
Purity:
≥ 99.5% (Chiral HPLC)
Synonym(s):
Boc-β-iodo-D-Ala-OMe
Documents
$113.87 /1G
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Product Information

Boc-3-iodo-D-alanine methyl ester is a versatile amino acid derivative that plays a crucial role in peptide synthesis and medicinal chemistry. This compound is particularly valued for its ability to introduce iodine into peptide sequences, which can enhance biological activity and facilitate the development of novel therapeutics. Its unique Boc (tert-butyloxycarbonyl) protecting group allows for selective deprotection, making it an ideal choice for researchers looking to manipulate peptide structures with precision.

In the pharmaceutical industry, Boc-3-iodo-D-alanine methyl ester is utilized in the design of bioactive compounds, including potential drug candidates targeting various diseases. Its application extends to the synthesis of radiolabeled peptides for imaging studies, providing insights into biological processes. Researchers benefit from its stability and ease of handling, which streamline the synthesis process and improve overall yields. This compound stands out among similar derivatives due to its specific iodine incorporation, which can significantly influence the pharmacokinetic properties of the resulting peptides.

Synonyms
Boc-β-iodo-D-Ala-OMe
CAS Number
170848-34-7
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C9H16INO4
Molecular Weight
329.14
MDL Number
MFCD00216580
PubChem ID
5051066
Melting Point
57 - 61 °C
Appearance
Pale yellow or white to off-white solid
Optical Rotation
[a]20D = -43 ± 2 º (C=1 in CHCl3)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-β-iodo-D-Ala-OMe
CAS Number
170848-34-7
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C9H16INO4
Molecular Weight
329.14
MDL Number
MFCD00216580
PubChem ID
5051066
Melting Point
57 - 61 °C
Appearance
Pale yellow or white to off-white solid
Optical Rotation
[a]20D = -43 ± 2 º (C=1 in CHCl3)
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-alanine methyl ester 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 incorporation of iodine, which can improve the pharmacological properties of drug candidates, making them more effective.
  • Bioconjugation: The compound is used in bioconjugation techniques, where it can be attached to biomolecules, aiding in the development of targeted therapies and diagnostic tools.
  • Research in Neuroscience: Due to its ability to mimic amino acids, it is employed in studies related to neurotransmitter function and receptor interactions, contributing to advancements in understanding neurological disorders.
  • Material Science: The compound can be utilized in the development of functional materials, such as hydrogels, which have applications in drug delivery systems and tissue engineering.

Citations