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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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Product Information

Conserver sous gaz inerte

Synonyms
( R )-(-)-nipécotate d'éthyle, Ester éthylique de l'acide ( R )-(-)-3-pipéridinecarboxylique
CAS Number
25137-01-3
Purity
≥ 98% (CG)
Molecular Formula
C 8 H 15 NO 2
Molecular Weight
157.21
MDL Number
MFCD03093637
PubChem ID
98969
Density
1.02
Appearance
Liquide clair incolore à presque incolore
Boiling Point
109 - 111 °C / 20 mmHg
Refractive Index
1.46
Optical Rotation
-1,0 à -2,0 degrés (pur)
Conditions
Conserver entre 2 et 8°C
General Information
Synonyms
( R )-(-)-nipécotate d'éthyle, Ester éthylique de l'acide ( R )-(-)-3-pipéridinecarboxylique
CAS Number
25137-01-3
Purity
≥ 98% (CG)
Molecular Formula
C 8 H 15 NO 2
Molecular Weight
157.21
MDL Number
MFCD03093637
PubChem ID
98969
Density
1.02
Appearance
Liquide clair incolore à presque incolore
Boiling Point
109 - 111 °C / 20 mmHg
Refractive Index
1.46
Optical Rotation
-1,0 à -2,0 degrés (pur)
Conditions
Conserver entre 2 et 8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
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.