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Catalog Number:
17340
CAS Number:
20583-31-7
3-(4-Nitrofenil)-1H - pirazol
Purity:
≥ 99 % (HPLC)
Synonym(s):
3-(4-Nitrofenil)pirazol
Documents
$52.88 /250 mg
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Product Information

3-(4-Nitrophenyl)-1H-pyrazole is a versatile compound recognized for its significant applications in various fields, particularly in pharmaceuticals and agrochemicals. This compound features a nitrophenyl group, which enhances its reactivity and makes it a valuable intermediate in the synthesis of bioactive molecules. Researchers often utilize 3-(4-Nitrophenyl)-1H-pyrazole in the development of novel pharmaceuticals, including anti-inflammatory and antimicrobial agents, due to its ability to modulate biological activity effectively. Additionally, its unique structure allows for the exploration of new agrochemical formulations aimed at improving crop protection and yield.

The compound's stability and reactivity make it an excellent candidate for further functionalization, enabling the creation of tailored derivatives with enhanced properties. Its application in the synthesis of pyrazole-based ligands has also garnered attention in coordination chemistry, where it plays a crucial role in developing catalysts and materials for various industrial processes. Overall, 3-(4-Nitrophenyl)-1H-pyrazole stands out for its potential to drive innovation in both research and industrial applications.

Synonyms
3-(4-Nitrofenil)pirazol
CAS Number
20583-31-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C9H7N3O2
Molecular Weight
189.17
MDL Number
MFCD00665859
PubChem ID
2737071
Melting Point
192-198 °C
Appearance
Agujas amarillas
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
3-(4-Nitrofenil)pirazol
CAS Number
20583-31-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C9H7N3O2
Molecular Weight
189.17
MDL Number
MFCD00665859
PubChem ID
2737071
Melting Point
192-198 °C
Appearance
Agujas amarillas
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-(4-Nitrophenyl)-1H-pyrazole is widely utilized in research focused on:

  • Agricultural Chemistry: This compound serves as an effective herbicide, helping to control unwanted plant growth in various crops, thus improving yield and quality.
  • Pharmaceutical Development: It is used in the synthesis of novel pharmaceutical agents, particularly in the development of anti-inflammatory and analgesic drugs.
  • Material Science: The compound finds applications in creating advanced materials, such as polymers and coatings, that require specific chemical properties for enhanced durability and performance.
  • Analytical Chemistry: It acts as a reagent in various analytical methods, aiding in the detection and quantification of other chemical substances in complex mixtures.
  • Biochemical Research: Researchers utilize it to study enzyme inhibition and receptor interactions, contributing to a better understanding of biological processes and disease mechanisms.

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