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Catalog Number:
33425
CAS Number:
171778-06-6
Acide Fmoc-3-amino-3-(2-nitro-phényl)-propionique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Lien ANP, Lien Fmoc-ANP
Documents
$80.00 /250 mg
Taille
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Informations sur le produit

Fmoc-3-amino-3-(2-nitro-phenyl)-propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. 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, characterized by the presence of a nitrophenyl group, enhances its reactivity and allows for the introduction of various functional groups, making it an invaluable tool for researchers in the development of novel therapeutic agents.

In practical applications, Fmoc-3-amino-3-(2-nitro-phenyl)-propionic acid is particularly beneficial in the synthesis of bioactive peptides and drug candidates, where precision and efficiency are paramount. Its ability to facilitate the formation of peptide bonds while maintaining stability under various reaction conditions makes it a preferred choice among chemists. Additionally, the compound's compatibility with solid-phase peptide synthesis (SPPS) techniques further underscores its significance in pharmaceutical research and development, enabling the streamlined production of complex peptide structures.

Numéro CAS 
171778-06-6
Formule moléculaire
C24H20N2O6
Poids moléculaire 
432.43
Informations générales
Numéro CAS 
171778-06-6
Formule moléculaire
C24H20N2O6
Poids moléculaire 
432.43
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Fmoc-3-amino-3-(2-nitro-phenyl)-propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis. Its protective Fmoc group allows for selective deprotection, facilitating the assembly of complex peptide structures.
  • Drug Development: The unique structural features of this compound make it valuable in the development of new pharmaceuticals, especially in creating compounds that target specific biological pathways or receptors.
  • Bioconjugation: It is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, enhancing the functionality of therapeutic agents or diagnostic tools.
  • Research in Neuroscience: The nitrophenyl group can be utilized in studies related to neurotransmitter activity, making it relevant for researchers exploring neurological disorders and potential treatments.
  • Material Science: This compound can be incorporated into polymer matrices, leading to the development of advanced materials with tailored properties for applications in coatings, adhesives, and drug delivery systems.

Citations