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Catalog Number:
04716
CAS Number:
185379-39-9
Fmoc-3-(2'-piridil)-D-alanina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-Ala(2'-piridil)-OH, Fmoc-b-(2'-piridil)-D-Ala-OH
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Product Information

Fmoc-3-(2'-pyridyl)-D-alanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, incorporating a pyridine ring, enhances the compound's ability to participate in various chemical reactions, making it a valuable building block in the creation of bioactive peptides and pharmaceuticals. Researchers appreciate its stability and compatibility with standard coupling reagents, which streamlines the synthesis process and improves yields.

In addition to its role in peptide synthesis, Fmoc-3-(2'-pyridyl)-D-alanine has potential applications in the development of targeted therapies and drug delivery systems. Its distinctive properties allow for the design of peptides with enhanced biological activity and specificity, which is crucial in the fields of medicinal chemistry and biochemistry. This compound stands out among similar derivatives due to its favorable reactivity and the ability to introduce functional groups that can modulate biological interactions, making it an essential tool for researchers aiming to innovate in peptide-based therapeutics.

Synonyms
Fmoc-D-Ala(2'-piridil)-OH, Fmoc-b-(2'-piridil)-D-Ala-OH
CAS Number
185379-39-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C23H20N2O4
Molecular Weight
388.4
MDL Number
MFCD00672565
PubChem ID
4600724
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-D-Ala(2'-piridil)-OH, Fmoc-b-(2'-piridil)-D-Ala-OH
CAS Number
185379-39-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C23H20N2O4
Molecular Weight
388.4
MDL Number
MFCD00672565
PubChem ID
4600724
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-3-(2'-pyridyl)-D-alanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase 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 pyridine moiety can facilitate the conjugation of biomolecules, enhancing the delivery and efficacy of therapeutic agents in targeted therapies.
  • Research in Neuroscience: This compound is used in studies exploring neuroactive peptides, contributing to the understanding of neurological functions and potential treatments for disorders.
  • Analytical Chemistry: It aids in the development of analytical methods for detecting and quantifying peptides, providing researchers with reliable tools for their studies.

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