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Catalog Number:
25559
CAS Number:
160436-48-6
Ethyl 3-amino-6-phenyl-4-(trifluoromethyl)furo(2,3-bpyridine-2-carboxylate
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Product Information

Ethyl 3-amino-6-phenyl-4-(trifluoromethyl)furo(2,3-b)pyridine-2-carboxylate is a versatile compound with significant applications in pharmaceutical research and development. This compound is recognized for its unique trifluoromethyl group, which enhances its biological activity and lipophilicity, making it an attractive candidate for drug design. Researchers have explored its potential in synthesizing novel therapeutic agents, particularly in the fields of oncology and neurology, where it may contribute to the development of targeted treatments.

Additionally, the compound's furo-pyridine structure provides a scaffold for further modifications, allowing chemists to tailor its properties for specific applications. Its ability to act as a building block in complex organic synthesis opens avenues for the creation of diverse chemical entities. Ethyl 3-amino-6-phenyl-4-(trifluoromethyl)furo(2,3-b)pyridine-2-carboxylate stands out for its potential to facilitate advancements in medicinal chemistry, making it a valuable resource for researchers and industry professionals alike.

CAS Number
160436-48-6
Molecular Formula
C17H13F3N2O3
Molecular Weight
350.3
MDL Number
MFCD03934051
PubChem ID
4457188
Conditions
Store at 0-8°C
General Information
CAS Number
160436-48-6
Molecular Formula
C17H13F3N2O3
Molecular Weight
350.3
MDL Number
MFCD03934051
PubChem ID
4457188
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 3-amino-6-phenyl-4-(trifluoromethyl)furo(2,3-b)pyridine-2-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, offering potential benefits in pest control due to its unique chemical structure that enhances efficacy against specific pests.
  • Material Science: The compound is explored for its properties in creating advanced materials, particularly in coatings that require enhanced durability 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.
  • Fluorinated Compound Research: Its trifluoromethyl group makes it a subject of interest in the study of fluorinated compounds, which are known for their unique chemical properties and applications in various fields.

Citations