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Catalog Number:
38095
CAS Number:
25137-01-3
( R )-(-)-3-pipéridinecarboxylate d'éthyle
Purity:
≥ 98% (CG)
Synonym(s):
( R )-(-)-nipécotate d'éthyle, Ester éthylique de l'acide ( R )-(-)-3-pipéridinecarboxylique
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Informations sur le produit

Conserver sous gaz inerte

Numéro CAS 
25137-01-3
Formule moléculaire
C 8 H 15 NO 2
Poids moléculaire 
157.21
Indice de réfraction 
1.46
Rotation optique 
-1,0 à -2,0 degrés (pur)
Informations générales
Numéro CAS 
25137-01-3
Formule moléculaire
C 8 H 15 NO 2
Poids moléculaire 
157.21
Indice de réfraction 
1.46
Rotation optique 
-1,0 à -2,0 degrés (pur)
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 
-
Applications

Ethyl (R)-(-)-3-piperidinecarboxylate is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as an important intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological disorders. Its chiral nature allows for the development of enantiomerically pure drugs, enhancing therapeutic efficacy.
  • Development of Agrochemicals: It is used in the formulation of agrochemicals, providing effective solutions for pest control. Its unique structure contributes to the development of safer and more efficient agricultural products.
  • Research in Organic Chemistry: As a versatile building block, it is employed in organic synthesis, allowing chemists to create complex molecules. This application is crucial for developing new materials and compounds in various research projects.
  • Biochemical Studies: The compound is utilized in biochemical research to study enzyme interactions and metabolic pathways. Its role in these studies helps researchers understand biological processes better, leading to potential medical advancements.
  • Chiral Catalysis: Ethyl (R)-(-)-3-piperidinecarboxylate is valuable in chiral catalysis, where it aids in the production of other chiral compounds. This application is significant in creating drugs with specific desired effects while minimizing side effects.

Citations