4-Fluoro-N-methylaniline
98%
- Product Code: 56743
CAS:
459-59-6
| Molecular Weight: | 125.15 g./mol | Molecular Formula: | C₇FH₈N |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00017942 | |
| Melting Point: | 79-80°C | Boiling Point: | |
| Density: | 1.1057g/mL | Storage Condition: | room temperature, dry |
Product Description:
4-Fluoro-N-methylaniline is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its structure makes it valuable for introducing fluorine and methylamine groups into more complex molecules, which can enhance the biological activity and stability of the final compounds. In the pharmaceutical industry, it is often employed in the production of drugs targeting central nervous system disorders, due to its ability to cross the blood-brain barrier. Additionally, it serves as a building block in the development of dyes and pigments, where its aromatic amine group contributes to color formation. The compound is also utilized in research and development for creating novel chemical entities with potential therapeutic applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | yellow to black liquid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿2,180.00 |
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| 25.000 | 10-20 days | ฿10,620.00 |
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4-Fluoro-N-methylaniline
4-Fluoro-N-methylaniline is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its structure makes it valuable for introducing fluorine and methylamine groups into more complex molecules, which can enhance the biological activity and stability of the final compounds. In the pharmaceutical industry, it is often employed in the production of drugs targeting central nervous system disorders, due to its ability to cross the blood-brain barrier. Additionally, it serves as a building block in the development of dyes and pigments, where its aromatic amine group contributes to color formation. The compound is also utilized in research and development for creating novel chemical entities with potential therapeutic applications.
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