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Catalog Number:
02905
CAS Number:
16652-71-4
Chlorhydrate d'ester benzylique de L-Proline
Purity:
≥ 98 % (HPLC)
Synonym(s):
L-Pro-OBzl·HCl, Chlorhydrate d'ester benzylique de l'acide ( S )-pyrrolidine-2-carboxylique
Documents
$18.53 /5G
Taille
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Informations sur le produit

L-Proline benzyl ester hydrochloride is a versatile compound widely utilized in the fields of organic synthesis and pharmaceutical research. This compound serves as an important building block in the synthesis of various bioactive molecules, particularly in the development of peptide-based drugs. Its unique structure allows for the introduction of proline residues into peptides, enhancing their stability and biological activity. Researchers appreciate its ability to facilitate the formation of cyclic peptides, which are known for their improved binding affinity and selectivity in biological systems.

In addition to its applications in drug discovery, L-Proline benzyl ester hydrochloride is also employed in the synthesis of chiral intermediates, making it invaluable in asymmetric synthesis processes. Its high purity and stability make it a preferred choice for researchers seeking reliable reagents for complex chemical reactions. With its potential to streamline synthetic pathways and improve the efficacy of pharmaceutical compounds, this ester hydrochloride is an essential tool for chemists and industry professionals alike.

Numéro CAS 
16652-71-4
Formule moléculaire
C12H15NO2 · HCl
Poids moléculaire 
241.7
Point de fusion 
138 - 152 ?C
Rotation optique 
[a] D 20 = -44 ± 2 º (C = 1 dans MeOH)
Informations générales
Numéro CAS 
16652-71-4
Formule moléculaire
C12H15NO2 · HCl
Poids moléculaire 
241.7
Point de fusion 
138 - 152 ?C
Rotation optique 
[a] D 20 = -44 ± 2 º (C = 1 dans MeOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

L-Proline benzyl ester hydrochloride is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in creating cyclic peptides that have enhanced stability and bioactivity.
  • Pharmaceutical Development: It is used in the development of various pharmaceuticals, especially those targeting neurological disorders, due to its ability to cross the blood-brain barrier effectively.
  • Chiral Catalysis: The compound acts as a chiral catalyst in asymmetric synthesis, allowing for the production of enantiomerically pure compounds, which is crucial in drug development.
  • Bioconjugation: It plays a role in bioconjugation processes, linking biomolecules to drugs or imaging agents, enhancing the specificity and efficacy of therapeutic agents.
  • Research in Organic Chemistry: Researchers leverage its unique properties to explore new synthetic pathways and reactions, contributing to advancements in organic chemistry methodologies.

Citations