4-Fluoroiodobenzene
99%, including 0.01% copper stabilizer
- Product Code: 118941
Alias:
4-fluoroiodobenzene; p-fluoroiodobenzene, 1-fluoro-4-iodobenzene
CAS:
352-34-1
| Molecular Weight: | 222 g./mol | Molecular Formula: | C₆H₄FI |
|---|---|---|---|
| EC Number: | 206-522-7 | MDL Number: | MFCD00001052 |
| Melting Point: | −20 °C(lit.) | Boiling Point: | 182-184 °C(lit.) |
| Density: | 1.925 g/mL at 25 °C(lit.) | Storage Condition: | Room temperature, away from light, dry |
Product Description:
4-Fluoroiodobenzene is widely used as a versatile intermediate in organic synthesis, particularly in the preparation of complex molecules. It serves as a key building block in the development of pharmaceuticals, where it is employed in cross-coupling reactions such as Suzuki, Sonogashira, and Heck reactions to introduce aromatic fluorine and iodine substituents. These reactions are crucial for creating biologically active compounds, including potential drug candidates. Additionally, it is utilized in material science for synthesizing advanced organic materials, such as liquid crystals and polymers, due to its ability to modify electronic and structural properties. Its role in agrochemical research is also notable, as it aids in the development of novel pesticides and herbicides.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 99-100 |
| Refractive Index N20/D | 1.582-1.584 |
| Specific Gravity (20/20) | 1.91-1.921 |
| Appearance | Colorless To Light Yellow Clear Liquid |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿290.00 |
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| 25.000 | 10-20 days | ฿890.00 |
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| 100.000 | 10-20 days | ฿2,450.00 |
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| 500.000 | 10-20 days | ฿9,860.00 |
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4-Fluoroiodobenzene
4-Fluoroiodobenzene is widely used as a versatile intermediate in organic synthesis, particularly in the preparation of complex molecules. It serves as a key building block in the development of pharmaceuticals, where it is employed in cross-coupling reactions such as Suzuki, Sonogashira, and Heck reactions to introduce aromatic fluorine and iodine substituents. These reactions are crucial for creating biologically active compounds, including potential drug candidates. Additionally, it is utilized in material science for synthesizing advanced organic materials, such as liquid crystals and polymers, due to its ability to modify electronic and structural properties. Its role in agrochemical research is also notable, as it aids in the development of novel pesticides and herbicides.
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