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Catalog Number:
05495
CAS Number:
65717-64-8
Nα-Boc-Nim-benzyl-D-histidine
Purity:
≥ 99% (TLC)
Synonym(s):
Boc-D-His(Bzl)-OH
Documents
$74.81 /1G
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Product Information

Na-Boc-Nim-benzyl-D-histidine is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a unique Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers focusing on the synthesis of complex peptides and biologically active compounds. Its structure, characterized by the benzyl and imidazole moieties, allows for versatile applications in medicinal chemistry, particularly in the design of peptide-based therapeutics and enzyme inhibitors.

In the pharmaceutical industry, Na-Boc-Nim-benzyl-D-histidine is utilized for its ability to facilitate the formation of peptide bonds, thereby streamlining the synthesis of bioactive peptides. This compound is particularly advantageous in the development of targeted therapies, where precision and efficacy are paramount. Researchers appreciate its compatibility with various coupling reagents and its ability to enhance the overall yield of peptide synthesis. With its unique properties and practical applications, Na-Boc-Nim-benzyl-D-histidine stands out as a valuable tool for professionals in the fields of biochemistry and pharmaceutical research.

Synonyms
Boc-D-His(Bzl)-OH
CAS Number
65717-64-8
Purity
≥ 99% (TLC)
Molecular Formula
C18H23N3O4
Molecular Weight
345.4
MDL Number
MFCD00038628
PubChem ID
89402
Melting Point
180-184º
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-D-His(Bzl)-OH
CAS Number
65717-64-8
Purity
≥ 99% (TLC)
Molecular Formula
C18H23N3O4
Molecular Weight
345.4
MDL Number
MFCD00038628
PubChem ID
89402
Melting Point
180-184º
Appearance
White powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Boc-Nim-benzyl-D-histidine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure makes it valuable in the design of novel pharmaceuticals, particularly in creating compounds that target specific biological pathways.
  • Bioconjugation: The compound can be used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in diagnostics and therapeutic applications.
  • Research on Protein Interactions: It aids in studying protein-protein interactions, helping researchers understand cellular mechanisms and develop targeted therapies.
  • Custom Synthesis: Its versatility allows for tailored synthesis in laboratories, meeting specific research needs in various fields such as biochemistry and molecular biology.

Citations