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Catalog Number:
25767
CAS Number:
155377-19-8
Ethyl 3-(trifluoromethyl)-1H-pyrazole-4-carboxylate
Purity:
≥ 99% (HPLC)
Synonym(s):
3-(Trifluoromethyl)pyrazole-4-carboxylic acid ethyl ester
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Product Information

Ethyl 3-(trifluoromethyl)-1H-pyrazole-4-carboxylate is a versatile compound recognized for its unique trifluoromethyl group, which enhances its reactivity and solubility in various organic solvents. This compound is particularly valuable in the pharmaceutical and agrochemical industries, where it serves as a key intermediate in the synthesis of bioactive molecules. Its ability to modify biological activity makes it an essential building block for developing new drugs and crop protection agents. Researchers have utilized this compound in the design of novel pyrazole derivatives, which have shown promising results in anti-inflammatory and anti-cancer studies.

In addition to its applications in drug discovery, Ethyl 3-(trifluoromethyl)-1H-pyrazole-4-carboxylate is also employed in materials science for the development of advanced polymers and coatings. Its trifluoromethyl group imparts desirable properties such as increased thermal stability and chemical resistance, making it suitable for high-performance applications. With its broad range of applications and unique properties, this compound is an excellent choice for researchers and industry professionals looking to innovate in their respective fields.

Synonyms
3-(Trifluoromethyl)pyrazole-4-carboxylic acid ethyl ester
CAS Number
155377-19-8
Purity
≥ 99% (HPLC)
Molecular Formula
C7H7F3N2O2
Molecular Weight
208.14
MDL Number
MFCD00052083
PubChem ID
596095
Melting Point
143-146 ?C
Appearance
White crystalline powder
Conditions
Store at 0-8°C
General Information
Synonyms
3-(Trifluoromethyl)pyrazole-4-carboxylic acid ethyl ester
CAS Number
155377-19-8
Purity
≥ 99% (HPLC)
Molecular Formula
C7H7F3N2O2
Molecular Weight
208.14
MDL Number
MFCD00052083
PubChem ID
596095
Melting Point
143-146 ?C
Appearance
White crystalline powder
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-(trifluoromethyl)-1H-pyrazole-4-carboxylate is widely utilized in research focused on:

  • Agricultural Chemistry: This compound serves as a key intermediate in the synthesis of agrochemicals, particularly fungicides and herbicides, enhancing crop protection and yield.
  • Pharmaceutical Development: It is used in the design of novel pharmaceuticals, especially in developing anti-inflammatory and analgesic agents, contributing to pain management solutions.
  • Material Science: The compound finds applications in creating advanced materials, such as polymers and coatings, that require specific thermal and chemical resistance properties.
  • Fluorine Chemistry: Its trifluoromethyl group makes it valuable in fluorine chemistry, allowing researchers to explore new fluorinated compounds with unique properties for various applications.
  • Research and Development: It is often employed in academic and industrial laboratories for synthesizing new chemical entities, facilitating innovation in various fields of chemistry.

Citations