1-Fluoro-4-nitronaphthalene
95% (HPLC)
- Product Code: 39886
CAS:
341-92-4
| Molecular Weight: | 191.16 g./mol | Molecular Formula: | C₁₀H₆FNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00156398 | |
| Melting Point: | Boiling Point: | 314.6°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
1-Fluoro-4-nitronaphthalene is primarily used in organic synthesis as an intermediate for the preparation of more complex chemical compounds. Its structure, featuring both a nitro group and a fluorine atom, makes it a valuable building block in the development of pharmaceuticals, agrochemicals, and dyes. The nitro group allows for further functionalization through reduction or substitution reactions, while the fluorine atom can enhance the stability and biological activity of the resulting molecules. Additionally, it is utilized in research settings to study electrophilic aromatic substitution reactions, providing insights into the reactivity and selectivity of aromatic systems. Its application extends to material science, where it contributes to the synthesis of organic electronic materials and fluorescent dyes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿783.00 |
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| 0.250 | 10-20 days | ฿1,566.00 |
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| 1.000 | 10-20 days | ฿2,484.00 |
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| 5.000 | 10-20 days | ฿10,287.00 |
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1-Fluoro-4-nitronaphthalene
1-Fluoro-4-nitronaphthalene is primarily used in organic synthesis as an intermediate for the preparation of more complex chemical compounds. Its structure, featuring both a nitro group and a fluorine atom, makes it a valuable building block in the development of pharmaceuticals, agrochemicals, and dyes. The nitro group allows for further functionalization through reduction or substitution reactions, while the fluorine atom can enhance the stability and biological activity of the resulting molecules. Additionally, it is utilized in research settings to study electrophilic aromatic substitution reactions, providing insights into the reactivity and selectivity of aromatic systems. Its application extends to material science, where it contributes to the synthesis of organic electronic materials and fluorescent dyes.
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