4-((1H-Pyrazol-1-yl)methyl)aniline
95%
- Product Code: 46004
CAS:
142335-61-3
| Molecular Weight: | 173.2144 g./mol | Molecular Formula: | C₁₀H₁₁N₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03422514 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex chemical structures. Its pyrazole and aniline functional groups make it particularly valuable in the synthesis of pharmaceutical compounds, especially those targeting specific biological pathways. Additionally, it is employed in the creation of agrochemicals, where its structural features contribute to the development of pesticides and herbicides with enhanced efficacy. The compound’s ability to act as a building block for heterocyclic compounds also makes it relevant in material science, particularly in the design of organic electronic materials and polymers. Its applications are driven by its reactivity and the potential to introduce specific functional groups into target molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $75.66 |
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4-((1H-Pyrazol-1-yl)methyl)aniline
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex chemical structures. Its pyrazole and aniline functional groups make it particularly valuable in the synthesis of pharmaceutical compounds, especially those targeting specific biological pathways. Additionally, it is employed in the creation of agrochemicals, where its structural features contribute to the development of pesticides and herbicides with enhanced efficacy. The compound’s ability to act as a building block for heterocyclic compounds also makes it relevant in material science, particularly in the design of organic electronic materials and polymers. Its applications are driven by its reactivity and the potential to introduce specific functional groups into target molecules.
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