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Catalog Number:
29433
CAS Number:
1067915-34-7
Ethyl 1-benzyl-5,5-difluoro-4-oxopiperidine-3-carboxylate
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$208.31 /100MG
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Product Information

Ethyl 1-benzyl-5,5-difluoro-4-oxopiperidine-3-carboxylate is a versatile compound known for its unique structural features, making it a valuable asset in pharmaceutical research and development. This compound exhibits significant potential in the synthesis of novel therapeutic agents, particularly in the fields of medicinal chemistry and drug discovery. Its difluorinated piperidine structure enhances biological activity, providing a promising scaffold for the development of new drugs targeting various diseases.

Researchers have utilized Ethyl 1-benzyl-5,5-difluoro-4-oxopiperidine-3-carboxylate in the design of inhibitors and modulators, showcasing its ability to influence biological pathways effectively. Its favorable properties, such as stability and reactivity, allow for straightforward modifications, enabling chemists to tailor compounds for specific applications. This compound stands out in comparison to similar derivatives due to its enhanced lipophilicity and potential for improved bioavailability, making it an attractive choice for professionals in the pharmaceutical industry seeking innovative solutions.

CAS Number
1067915-34-7
Molecular Formula
C15H17F2NO3
Molecular Weight
297.3
MDL Number
MFCD16036533
PubChem ID
49761228
Conditions
Store at 0-8°C
General Information
CAS Number
1067915-34-7
Molecular Formula
C15H17F2NO3
Molecular Weight
297.3
MDL Number
MFCD16036533
PubChem ID
49761228
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ethyl 1-benzyl-5,5-difluoro-4-oxopiperidine-3-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of novel pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, providing enhanced efficacy in pest control products, which can lead to improved crop yields.
  • Material Science: The compound can be incorporated into polymer formulations, enhancing properties such as flexibility and resistance to environmental factors.
  • Biochemical Research: Researchers utilize it in studies related to enzyme inhibition, helping to understand metabolic pathways and develop new therapeutic strategies.
  • Fluorine Chemistry: Its unique difluoro group makes it valuable in fluorine chemistry research, offering insights into the behavior of fluorinated compounds in various applications.

Citations