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Catalog Number:
25073
CAS Number:
14678-87-6
5-amino-1-(4-chlorophényl)-pyrazole-4-carboxylate d'éthyle
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ester éthylique de l'acide 5-amino-1-(4-chloro-phényl)-1 H -pyrazole-4-carboxylique
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Product Information

Ethyl 5-amino-1-(4-chlorophenyl)-pyrazole-4-carboxylate is a versatile compound with significant applications in pharmaceuticals and agrochemicals. This compound is recognized for its potential as an intermediate in the synthesis of various bioactive molecules, particularly in the development of anti-inflammatory and analgesic agents. Its unique structure, featuring a pyrazole ring and a chlorophenyl group, enhances its reactivity and allows for modifications that can lead to the discovery of new therapeutic agents. Researchers have utilized this compound in the design of novel drugs, showcasing its importance in medicinal chemistry.

In addition to its pharmaceutical relevance, Ethyl 5-amino-1-(4-chlorophenyl)-pyrazole-4-carboxylate has shown promise in agricultural applications, particularly as a building block for herbicides and fungicides. Its ability to inhibit specific biological pathways makes it a valuable asset in crop protection formulations. The compound's favorable solubility and stability further enhance its usability in various formulations, making it an attractive choice for researchers and industry professionals seeking effective solutions in both health and agriculture.

Synonyms
Ester éthylique de l'acide 5-amino-1-(4-chloro-phényl)-1 H -pyrazole-4-carboxylique
CAS Number
14678-87-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C12H12ClN3O2
Molecular Weight
265.7
MDL Number
MFCD00973905
PubChem ID
4101804
Melting Point
148-154 ?C
Appearance
Poudre blanche
Conditions
Conserver à 0-8°C
General Information
Synonyms
Ester éthylique de l'acide 5-amino-1-(4-chloro-phényl)-1 H -pyrazole-4-carboxylique
CAS Number
14678-87-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C12H12ClN3O2
Molecular Weight
265.7
MDL Number
MFCD00973905
PubChem ID
4101804
Melting Point
148-154 ?C
Appearance
Poudre blanche
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 5-amino-1-(4-chlorophenyl)-pyrazole-4-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and analgesic drugs.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, enhancing crop protection products by acting as a herbicide or fungicide.
  • Biochemical Research: Researchers employ this compound to study its effects on biological pathways, contributing to the understanding of disease mechanisms and potential therapeutic targets.
  • Material Science: This chemical is explored for its potential in creating novel materials with specific properties, such as improved thermal stability and chemical resistance.
  • Analytical Chemistry: It is utilized as a reference standard in analytical methods, aiding in the accurate detection and quantification of related compounds in various samples.

Citations