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Catalog Number:
03132
CAS Number:
2812-46-6
Ester tert -butylique de L-Proline
Purity:
≥ 98 % (HPLC)
Synonym(s):
L-Pro-OtBu, ( Ester tert -butylique de l'acide S -pyrrolidine-2-carboxylique
Documents
$22.83 /1G
Taille
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Informations sur le produit

L-Proline tert-butyl ester is a versatile compound widely utilized in the synthesis of various pharmaceuticals and agrochemicals. This ester derivative of proline is particularly valued for its role as a chiral building block in asymmetric synthesis, enabling the production of enantiomerically pure compounds. Its unique structure allows for enhanced solubility and stability, making it an ideal candidate for applications in peptide synthesis and drug formulation. Researchers appreciate its utility in the development of novel therapeutic agents, especially in the fields of medicinal chemistry and biochemistry.

Additionally, L-Proline tert-butyl ester serves as an effective intermediate in the preparation of proline-based catalysts and ligands, which are crucial in various catalytic processes. Its favorable properties, such as low toxicity and high reactivity, position it as a preferred choice for professionals looking to streamline their synthesis routes while maintaining high yields. The compound's ability to facilitate complex reactions with minimal side products further underscores its significance in both academic and industrial settings.

Numéro CAS 
2812-46-6
Formule moléculaire
C 9 H 17 NO 2
Poids moléculaire 
171.2
Rotation optique 
[a] D 20 = - 42 ± 2 º (C=1 dans EtOH)
Informations générales
Numéro CAS 
2812-46-6
Formule moléculaire
C 9 H 17 NO 2
Poids moléculaire 
171.2
Rotation optique 
[a] D 20 = - 42 ± 2 º (C=1 dans EtOH)
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

L-Proline tert-butyl ester is widely utilized in research focused on:

  • Synthesis of Peptides: This compound serves as a valuable building block in peptide synthesis, allowing researchers to create specific sequences for pharmaceuticals and biologically active compounds.
  • Chiral Auxiliary in Organic Reactions: It acts as a chiral auxiliary, enhancing the selectivity of reactions in asymmetric synthesis, which is crucial for producing enantiomerically pure compounds in medicinal chemistry.
  • Drug Development: The ester form improves the solubility and bioavailability of proline derivatives, making it beneficial in the formulation of new drugs.
  • Biochemical Research: It is used in studies involving protein folding and enzyme activity, helping scientists understand the role of proline in biological systems.
  • Material Science: This compound is explored for its potential in developing new polymers and materials due to its unique structural properties.

Citations