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Catalog Number:
02478
CAS Number:
112883-39-3
Ester β- tert -butylique de l'acide Fmoc-D-aspartique
Purity:
≥ 99,5 % (HPLC chirale)
Synonym(s):
Fmoc-D-Asp(OtBu)-OH
Documents
$20.00 /1G
Taille
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Informations sur le produit

Fmoc-D-aspartic acid b-tert-butyl ester is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which is crucial for the selective protection of the amino group during the synthesis of peptides. Its tert-butyl ester moiety enhances solubility and stability, making it an excellent choice for various organic synthesis applications. Researchers appreciate its role in facilitating the formation of peptide bonds, particularly in the synthesis of complex peptides and proteins, which are essential in pharmaceuticals and biotechnology.

This compound is particularly beneficial in the development of peptide-based therapeutics, where precise control over amino acid sequences is vital. Its unique structure allows for easy deprotection under mild conditions, ensuring that the integrity of sensitive functional groups is maintained throughout the synthesis process. Additionally, Fmoc-D-aspartic acid b-tert-butyl ester can be employed in the preparation of peptide libraries for drug discovery, providing researchers with a powerful tool to explore new therapeutic avenues.

Numéro CAS 
112883-39-3
Formule moléculaire
C 23 H 256
Poids moléculaire 
411.5
Point de fusion 
145 - 160 °C
Rotation optique 
[a] D 20
Informations générales
Numéro CAS 
112883-39-3
Formule moléculaire
C 23 H 256
Poids moléculaire 
411.5
Point de fusion 
145 - 160 °C
Rotation optique 
[a] D 20
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-aspartic acid b-tert-butyl ester 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, allowing researchers to create complex peptide sequences with high efficiency.
  • Drug Development: Its role in drug design is significant, especially in developing neuroactive compounds. The ability to modify its structure can lead to the discovery of new therapeutics targeting neurological disorders.
  • Bioconjugation: This chemical is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial for creating targeted drug delivery systems.
  • Research in Neuroscience: It is employed in studies related to neurotransmitter pathways, helping researchers understand the mechanisms of action for various neuropeptides and their implications in brain function.
  • Modification of Amino Acids: The compound allows for the modification of amino acids in proteins, enhancing their stability and functionality, which is essential for various applications in biotechnology and pharmaceuticals.

Citations