N-(4-Methoxyphenyl)pyridin-4-amine
95%
- Product Code: 50245
CAS:
35488-09-6
| Molecular Weight: | 200.2400 g./mol | Molecular Formula: | C₁₂H₁₂N₂O |
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| EC Number: | MDL Number: | MFCD00982631 | |
| 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 key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring both pyridine and methoxyphenyl groups, makes it a versatile building block for the development of compounds with potential biological activity. Specifically, it is often employed in the synthesis of molecules that exhibit antimicrobial, anti-inflammatory, or anticancer properties. Additionally, its use extends to material science, where it can be incorporated into the design of organic electronic materials, such as organic light-emitting diodes (OLEDs) or conductive polymers, due to its electron-donating characteristics. The compound’s ability to participate in diverse chemical reactions also makes it valuable in research and development for creating novel chemical entities with tailored properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,439.00 |
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N-(4-Methoxyphenyl)pyridin-4-amine
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring both pyridine and methoxyphenyl groups, makes it a versatile building block for the development of compounds with potential biological activity. Specifically, it is often employed in the synthesis of molecules that exhibit antimicrobial, anti-inflammatory, or anticancer properties. Additionally, its use extends to material science, where it can be incorporated into the design of organic electronic materials, such as organic light-emitting diodes (OLEDs) or conductive polymers, due to its electron-donating characteristics. The compound’s ability to participate in diverse chemical reactions also makes it valuable in research and development for creating novel chemical entities with tailored properties.
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