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Catalog Number:
41576
CAS Number:
114636-37-2
( S )-(-)-1-Boc-3-acétamidopyrrolidine
Purity:
≥ 97% (CG)
Synonym(s):
tert -butyl(3 S )-3-(acétylamino)-1-pyrrolidinecarboxylate
Documents
$131.90 /1G
Taille
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Informations sur le produit

(S)-(-)-1-Boc-3-acetamidopyrrolidine is a versatile compound widely utilized in the pharmaceutical and chemical industries. This chiral building block is essential for the synthesis of various bioactive molecules, particularly in the development of pharmaceuticals targeting neurological disorders and other therapeutic areas. Its unique structure, featuring a tert-butyl carbamate protecting group, enhances its stability and reactivity, making it an ideal candidate for complex organic synthesis. Researchers appreciate its ability to facilitate the formation of intricate molecular architectures while maintaining high enantiomeric purity.

In addition to its applications in drug development, (S)-(-)-1-Boc-3-acetamidopyrrolidine serves as a valuable intermediate in the synthesis of peptide and heterocyclic compounds. Its compatibility with various coupling reactions allows for efficient incorporation into larger molecular frameworks, streamlining the synthesis process. This compound's favorable properties and practical applications make it an essential tool for chemists and researchers aiming to innovate in the fields of medicinal chemistry and organic synthesis.

Numéro CAS 
114636-37-2
Formule moléculaire
C11H20N2O3
Poids moléculaire 
228.29
Point de fusion 
86 - 90 °C
Rotation optique 
[ á]20/D = -18 ° (C = 3,5 dans le méthanol)
Informations générales
Numéro CAS 
114636-37-2
Formule moléculaire
C11H20N2O3
Poids moléculaire 
228.29
Point de fusion 
86 - 90 °C
Rotation optique 
[ á]20/D = -18 ° (C = 3,5 dans le méthanol)
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

(S)-(-)-1-Boc-3-acetamidopyrrolidine is widely utilized in research focused on

  • Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly in the development of drugs targeting neurological disorders.
  • Peptide Synthesis: It is used in the preparation of peptide-based therapeutics, enhancing the stability and bioavailability of the resulting compounds.
  • Chiral Building Block: As a chiral building block, it plays a crucial role in asymmetric synthesis, allowing chemists to create compounds with specific stereochemistry, which is vital in drug design.
  • Research in Medicinal Chemistry: It is employed in medicinal chemistry research to explore new drug candidates, particularly those that require modification of amino acid structures.
  • Bioconjugation Techniques: The compound can be utilized in bioconjugation methods, facilitating the attachment of drugs to biomolecules, which can improve targeted delivery in therapeutic applications.

Citations