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Catalog Number:
25028
CAS Number:
866588-11-6
3-(4-fluorophényl)-1 H -pyrazole-5-carboxylate d'éthyle
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ester éthylique de l'acide 3-(4-fluorophényl)-1 H -pyrazole-5-carboxylique
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$67.60 /100 mg
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Product Information

Ethyl 3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate is a versatile compound known for its potential applications in pharmaceutical research and development. This pyrazole derivative exhibits unique properties that make it a valuable building block in the synthesis of various biologically active molecules. Its structural features allow for modifications that can enhance its efficacy in targeting specific biological pathways, making it an attractive candidate for drug discovery and development.

Researchers have utilized Ethyl 3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate in the design of novel therapeutic agents, particularly in the fields of anti-inflammatory and anti-cancer treatments. Its ability to selectively interact with certain receptors can lead to the development of more effective medications with fewer side effects compared to traditional compounds. Additionally, its stability and ease of synthesis make it a preferred choice for laboratories focused on innovative drug formulations.

Synonyms
Ester éthylique de l'acide 3-(4-fluorophényl)-1 H -pyrazole-5-carboxylique
CAS Number
866588-11-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C12H11FN2O2
Molecular Weight
234.23
MDL Number
MFCD08445938
PubChem ID
583549
Melting Point
154-160 ?C
Appearance
Solide cristallin blanc
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Ester éthylique de l'acide 3-(4-fluorophényl)-1 H -pyrazole-5-carboxylique
CAS Number
866588-11-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C12H11FN2O2
Molecular Weight
234.23
MDL Number
MFCD08445938
PubChem ID
583549
Melting Point
154-160 ?C
Appearance
Solide cristallin blanc
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Ethyl 3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting inflammatory diseases, due to its ability to modulate specific biological pathways.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, providing effective solutions for pest control while minimizing environmental impact, making it a preferred choice for sustainable agriculture.
  • Material Science: The compound is explored for its potential in developing new materials with unique properties, such as enhanced thermal stability and chemical resistance, which are crucial for industrial applications.
  • Biochemical Research: Researchers utilize it in studies related to enzyme inhibition and receptor binding, contributing to a better understanding of various biochemical processes and disease mechanisms.
  • Analytical Chemistry: It is employed as a standard reference material in analytical methods, aiding in the calibration of instruments and ensuring accurate measurement of similar compounds in complex mixtures.

Citations