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Catalog Number:
41588
CAS Number:
131852-53-4
( S )-(-)-1-Benzyl-3-(Boc-amino)pyrrolidine
Purity:
≥ 97%
Synonym(s):
( S )-(-)-1-Benzyl-3-( tert -butoxycarbonylamino)pyrrolidine
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$104.26 /1G
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Informations sur le produit

(S)-(-)-1-Benzyl-3-(Boc-amino)pyrrolidine is a versatile compound widely utilized in pharmaceutical research and organic synthesis. This chiral pyrrolidine derivative features a benzyl group and a tert-butoxycarbonyl (Boc) protecting group, making it an essential building block in the development of various bioactive molecules. Its unique structure allows for the synthesis of complex compounds, particularly in the creation of peptide mimetics and other medicinal chemistry applications. Researchers appreciate its ability to enhance solubility and stability in formulations, which is crucial for drug development.

In addition to its role in synthetic chemistry, (S)-(-)-1-Benzyl-3-(Boc-amino)pyrrolidine has shown potential in the development of novel therapeutic agents, particularly in the fields of neuropharmacology and anti-cancer research. Its chiral nature provides an advantage in producing enantiomerically pure compounds, which are often required for optimal biological activity. This compound's relevance in current research trends underscores its importance for professionals seeking reliable and effective intermediates in their work.

Numéro CAS 
131852-53-4
Formule moléculaire
C16H24N2O2
Poids moléculaire 
276.37
Point de fusion 
77 - 81 °C (lit.)
Rotation optique 
[ á]20/D = -6 ° (C = 1 dans le chloroforme)
Informations générales
Numéro CAS 
131852-53-4
Formule moléculaire
C16H24N2O2
Poids moléculaire 
276.37
Point de fusion 
77 - 81 °C (lit.)
Rotation optique 
[ á]20/D = -6 ° (C = 1 dans le chloroforme)
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-Benzyl-3-(Boc-amino)pyrrolidine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly in the development of novel drugs targeting neurological disorders.
  • Peptide Synthesis: It is commonly used in peptide coupling reactions, enhancing the efficiency of synthesizing complex peptides that are crucial for drug discovery and development.
  • Chiral Catalysis: The compound acts as a chiral auxiliary in asymmetric synthesis, helping researchers create specific enantiomers that are often more effective in therapeutic applications.
  • Research in Neuroscience: It is utilized in studies exploring the mechanisms of action of neurotransmitters, aiding in the understanding of brain function and the development of treatments for mental health disorders.
  • Material Science: This chemical is also applied in the formulation of advanced materials, contributing to innovations in drug delivery systems and biocompatible polymers.

Citations