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Catalog Number:
25471
CAS Number:
618070-61-4
Ethyl 5-(trifluoromethyl)-1-(2-fluorophenyl)-1H-pyrazole-4-carboxylate
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$103.56 /100MG
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Product Information

Ethyl 5-(trifluoromethyl)-1-(2-fluorophenyl)-1H-pyrazole-4-carboxylate is a versatile compound known for its unique trifluoromethyl and fluorophenyl substituents, which enhance its reactivity and potential applications in various fields. This compound is particularly valuable in medicinal chemistry, where it serves as a key intermediate in the synthesis of bioactive molecules, including pharmaceuticals and agrochemicals. Its distinct structure allows for the development of compounds with improved efficacy and selectivity, making it an essential building block for researchers focused on drug discovery and development.

In addition to its applications in pharmaceuticals, Ethyl 5-(trifluoromethyl)-1-(2-fluorophenyl)-1H-pyrazole-4-carboxylate is also utilized in materials science and chemical research. Its unique properties can lead to the creation of innovative materials with specific functionalities. Researchers and industry professionals can leverage this compound to explore new avenues in their projects, benefiting from its high reactivity and the potential for diverse applications.

CAS Number
618070-61-4
Molecular Formula
C13H10F4N2O2
Molecular Weight
302.23
MDL Number
MFCD03934804
PubChem ID
5085411
Conditions
Store at 0-8°C
General Information
CAS Number
618070-61-4
Molecular Formula
C13H10F4N2O2
Molecular Weight
302.23
MDL Number
MFCD03934804
PubChem ID
5085411
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 5-(trifluoromethyl)-1-(2-fluorophenyl)-1H-pyrazole-4-carboxylate is widely utilized in research focused on:

  • Agricultural Chemistry: This compound is used in the development of new agrochemicals, particularly as a potential herbicide or fungicide, due to its ability to inhibit specific biological pathways in plants.
  • Pharmaceutical Development: It serves as a key intermediate in the synthesis of novel pharmaceuticals, particularly in the search for new anti-inflammatory or analgesic agents, leveraging its unique molecular structure.
  • Material Science: The compound is explored for its properties in creating advanced materials, such as polymers with enhanced thermal stability and chemical resistance, which are valuable in various industrial applications.
  • Biochemical Research: Researchers utilize it to study enzyme interactions and metabolic pathways, providing insights into disease mechanisms and potential therapeutic targets.
  • Fluorine Chemistry: Its trifluoromethyl group makes it a valuable tool in fluorine chemistry, allowing scientists to explore new fluorinated compounds that exhibit unique reactivity and stability.

Citations