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Catalog Number:
25121
CAS Number:
618070-50-1
3-(4-bromophényl)-1-méthyl-1 H -pyrazole-5-carboxylate d'éthyle
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ester éthylique de l'acide 3-(4-bromophényl)-1-méthyl-1 H -pyrazole-5-carboxylique
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$110.57 /100 mg
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Product Information

Ethyl 3-(4-bromophenyl)-1-methyl-1H-pyrazole-5-carboxylate is a versatile compound recognized for its significant applications in pharmaceutical research and development. This compound features a unique pyrazole structure, which contributes to its potential as a building block in the synthesis of various bioactive molecules. Its bromophenyl group enhances its reactivity, making it an attractive candidate for medicinal chemistry, particularly in the development of new therapeutic agents targeting various diseases.

Researchers have utilized Ethyl 3-(4-bromophenyl)-1-methyl-1H-pyrazole-5-carboxylate in the design of novel anti-inflammatory and analgesic compounds, showcasing its efficacy in drug discovery. Additionally, its properties lend themselves well to applications in agrochemicals, where it can be employed in the formulation of effective crop protection agents. The compound's stability and ease of modification further enhance its appeal, allowing for tailored applications in diverse fields.

Synonyms
Ester éthylique de l'acide 3-(4-bromophényl)-1-méthyl-1 H -pyrazole-5-carboxylique
CAS Number
618070-50-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C13H13BrN2O2
Molecular Weight
309.16
MDL Number
MFCD03933290
PubChem ID
4605409
Melting Point
89-95 ?C
Appearance
Poudre blanche
Conditions
Conserver à 0-8°C
General Information
Synonyms
Ester éthylique de l'acide 3-(4-bromophényl)-1-méthyl-1 H -pyrazole-5-carboxylique
CAS Number
618070-50-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C13H13BrN2O2
Molecular Weight
309.16
MDL Number
MFCD03933290
PubChem ID
4605409
Melting Point
89-95 ?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 3-(4-bromophenyl)-1-methyl-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 in developing anti-inflammatory and analgesic medications.
  • Agricultural Chemistry: It is used in formulating agrochemicals, contributing to the development of effective pesticides and herbicides that target specific pests while minimizing environmental impact.
  • Material Science: The compound is explored for its potential in creating novel materials, including polymers and coatings, that exhibit enhanced durability and resistance to environmental stressors.
  • Biochemical Research: Researchers utilize it to study enzyme interactions and metabolic pathways, aiding in the understanding of biological processes and disease mechanisms.
  • Analytical Chemistry: It is employed as a standard reference material in analytical methods, ensuring accuracy and reliability in the quantification of similar compounds in various samples.

Citations