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Catalog Number:
02454
CAS Number:
71989-33-8
Fmoc- O - tert -butyl-L-sérine
Purity:
≥ 99,5 % (HPLC chirale, HPLC)
Synonym(s):
Fmoc-L-Ser(tBu)-OH
Documents
$25.00 /5G
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Informations sur le produit

Fmoc-O-tert-butyl-L-serine is a versatile amino acid derivative widely utilized in peptide synthesis and bioconjugation applications. This compound features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which allows for selective deprotection during the synthesis of peptides, making it an essential building block for researchers in the field of medicinal chemistry and drug development. Its tert-butyl group enhances solubility and stability, facilitating smoother reactions and improving yields in complex synthetic pathways.

Researchers and industry professionals appreciate Fmoc-O-tert-butyl-L-serine for its role in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. This compound is particularly advantageous in solid-phase peptide synthesis (SPPS), where its protective groups can be easily removed under mild conditions, allowing for the efficient assembly of peptides. Its unique properties make it a preferred choice for those looking to streamline their synthesis processes while achieving high purity and functionality in their final products.

Numéro CAS 
71989-33-8
Formule moléculaire
C 22 H 255
Poids moléculaire 
383.4
Point de fusion 
125 - 140 °C
Rotation optique 
[a] D 20 = 25 ± 3 º (C = 1 dans EtOAc)
Informations générales
Numéro CAS 
71989-33-8
Formule moléculaire
C 22 H 255
Poids moléculaire 
383.4
Point de fusion 
125 - 140 °C
Rotation optique 
[a] D 20 = 25 ± 3 º (C = 1 dans EtOAc)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
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Applications

Fmoc-O-tert-butyl-L-serine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group for the amino acid serine during peptide synthesis, allowing for the selective modification of other amino acids without affecting serine.
  • Drug Development: It plays a crucial role in the design of peptide-based therapeutics, particularly in the development of drugs targeting specific biological pathways.
  • Bioconjugation: Researchers use it to facilitate the attachment of biomolecules to surfaces or other molecules, enhancing the efficacy of diagnostics and therapeutics.
  • Protein Engineering: The compound is used in the modification of proteins to improve their stability and functionality, which is essential in various biotechnological applications.
  • Research in Neuroscience: It is applied in studies involving neurotransmitter systems, where modified peptides can help in understanding receptor interactions and signaling pathways.

Citations