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Catalog Number:
03620
CAS Number:
125043-04-1
Ester pentafluorophénylique de Fmoc-D-alanine
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-D-Ala-OPfp
Documents
$52.88 /1G
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Informations sur le produit

Fmoc-D-alanine pentafluorophenyl ester is a highly versatile compound widely utilized in peptide synthesis and drug development. This compound serves as a valuable building block for the preparation of peptides, particularly in solid-phase peptide synthesis (SPPS), due to its stability and ease of handling. The presence of the Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection under mild conditions, making it an ideal choice for researchers aiming to construct complex peptide sequences efficiently. Its pentafluorophenyl ester moiety enhances the reactivity and solubility of the compound, facilitating smoother reactions and higher yields in synthetic processes.

In addition to its applications in peptide synthesis, Fmoc-D-alanine pentafluorophenyl ester is also relevant in the development of pharmaceuticals and biologically active compounds. Its unique properties allow for the incorporation of D-amino acids into peptides, which can significantly influence the biological activity and stability of the resulting molecules. This compound is particularly beneficial for researchers focused on designing peptides with enhanced therapeutic potential, making it a crucial tool in the fields of medicinal chemistry and biochemistry.

Numéro CAS 
125043-04-1
Formule moléculaire
C 24 H 16 F 5 NON 4
Poids moléculaire 
477.4
Point de fusion 
173-179 °C
Rotation optique 
[α] D = +20 ± 2º (C=1 dans CHCl3)
Informations générales
Numéro CAS 
125043-04-1
Formule moléculaire
C 24 H 16 F 5 NON 4
Poids moléculaire 
477.4
Point de fusion 
173-179 °C
Rotation optique 
[α] D = +20 ± 2º (C=1 dans CHCl3)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Fmoc-D-alanine pentafluorophenyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, enabling researchers to create complex molecules for drug development and biological studies.
  • Protein Engineering: Its unique structure allows for the selective modification of amino acids in proteins, facilitating the design of proteins with enhanced stability and functionality.
  • Drug Discovery: By using this ester in high-throughput screening, pharmaceutical companies can identify potential drug candidates more efficiently, speeding up the development process.
  • Bioconjugation: The pentafluorophenyl group provides excellent reactivity for bioconjugation applications, allowing for the attachment of various biomolecules, which is crucial in creating targeted therapies.
  • Analytical Chemistry: It is utilized in analytical methods for the detection and quantification of peptides, aiding researchers in characterizing new compounds and understanding their properties.

Citations