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Catalog Number:
03737
CAS Number:
111061-56-4
Fmoc- O -trityl-L-sérine
Purity:
≥ 99,5 % (HPLC, pureté chirale)
Synonym(s):
Fmoc-L-Ser(Trt)-OH
Documents
$22.83 /1G
Taille
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Informations sur le produit

Fmoc-O-trityl-L-serine is a highly versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which allows for selective deprotection during the synthesis process, making it an essential building block for the creation of complex peptides. Its trityl (Tr) protection enhances stability and solubility, facilitating its use in various organic reactions. Researchers and industry professionals appreciate its role in solid-phase peptide synthesis, where it enables the efficient assembly of peptides with high purity and yield.

In addition to its applications in peptide synthesis, Fmoc-O-trityl-L-serine is also valuable in the development of pharmaceuticals and bioconjugates. Its unique properties allow for the incorporation of serine residues into peptides, which can be crucial for biological activity and specificity. This compound stands out for its ability to streamline the synthesis process while maintaining the integrity of sensitive functional groups, making it a preferred choice for chemists and researchers in the field.

Numéro CAS 
111061-56-4
Formule moléculaire
C 37 H 315
Poids moléculaire 
569.7
Point de fusion 
200-210 ºC
Rotation optique 
[a] D 20 = + 8 ± 1º (C = 1 dans DMF)
Informations générales
Numéro CAS 
111061-56-4
Formule moléculaire
C 37 H 315
Poids moléculaire 
569.7
Point de fusion 
200-210 ºC
Rotation optique 
[a] D 20 = + 8 ± 1º (C = 1 dans DMF)
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-O-trityl-L-serine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group for the amino acid serine during solid-phase peptide synthesis, allowing for the selective modification of peptides without unwanted reactions.
  • Drug Development: Its role in synthesizing bioactive peptides makes it valuable in pharmaceutical research, particularly in developing new therapeutics targeting various diseases.
  • Bioconjugation: The compound can be used to create bioconjugates, which are essential in developing targeted drug delivery systems, enhancing the efficacy of treatments.
  • Protein Engineering: Researchers utilize it to modify proteins, improving their stability and functionality, which is crucial in biotechnology applications.
  • Analytical Chemistry: Fmoc-O-trityl-L-serine is used in various analytical techniques, including mass spectrometry, to study peptide structures and interactions.

Citations