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Catalog Number:
38095
CAS Number:
25137-01-3
( R )-(-)-3-piperidinacarboxilato de etilo
Purity:
≥ 98% (GC)
Synonym(s):
( R )-(-)-nipecotato de etilo, Éster etílico del ácido ( R )-(-)-3-piperidinacarboxílico
Documents
$141.41 /5G
Tamaño
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Product Information

Conservar bajo gas inerte.

Synonyms
( R )-(-)-nipecotato de etilo, Éster etílico del ácido ( R )-(-)-3-piperidinacarboxílico
CAS Number
25137-01-3
Purity
≥ 98% (GC)
Molecular Formula
C8H15NO2
Molecular Weight
157.21
MDL Number
MFCD03093637
PubChem ID
98969
Density
1.02
Appearance
Líquido transparente incoloro a casi incoloro.
Boiling Point
109-111 °C / 20 mmHg
Refractive Index
1.46
Optical Rotation
-1,0 a -2,0 grados (puro)
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
( R )-(-)-nipecotato de etilo, Éster etílico del ácido ( R )-(-)-3-piperidinacarboxílico
CAS Number
25137-01-3
Purity
≥ 98% (GC)
Molecular Formula
C8H15NO2
Molecular Weight
157.21
MDL Number
MFCD03093637
PubChem ID
98969
Density
1.02
Appearance
Líquido transparente incoloro a casi incoloro.
Boiling Point
109-111 °C / 20 mmHg
Refractive Index
1.46
Optical Rotation
-1,0 a -2,0 grados (puro)
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
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.