4-Fluoro-2-iodotoluene
98%
- Product Code: 118915
Alias:
4-fluoro-2-iodo-1-methylbenzene
CAS:
13194-67-7
| Molecular Weight: | 236.03 g./mol | Molecular Formula: | IC₆H₃FCH₃ |
|---|---|---|---|
| EC Number: | 236-153-7 | MDL Number: | MFCD00013709 |
| Melting Point: | Boiling Point: | 92-94 °C15 mm Hg(lit.) | |
| Density: | 1.752 g/mL at 25 °C(lit.) | Storage Condition: | room temperature |
Product Description:
4-Fluoro-2-iodotoluene is primarily used in organic synthesis as a versatile building block for the development of more complex chemical compounds. Its structure, featuring both fluorine and iodine substituents, makes it valuable in cross-coupling reactions, such as Suzuki and Sonogashira couplings, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. The presence of the iodine atom allows for easy functionalization, enabling the introduction of various other groups to the aromatic ring. Additionally, the fluorine atom can enhance the biological activity and metabolic stability of the final products, making it particularly useful in drug discovery and development. This compound is also employed in the synthesis of liquid crystals and organic electronic materials, where its unique electronic properties contribute to the desired performance characteristics.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 98-100 |
| Refractive Index N20/D | 1.577-1.581 |
| Specific Gravity (20/20) | 1.809-1.813 |
| Appearance | Colorless To Yellow Liquid |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $14.09 |
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| 5.000 | 10-20 days | $32.41 |
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| 25.000 | 10-20 days | $102.38 |
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| 100.000 | 10-20 days | $397.32 |
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4-Fluoro-2-iodotoluene
4-Fluoro-2-iodotoluene is primarily used in organic synthesis as a versatile building block for the development of more complex chemical compounds. Its structure, featuring both fluorine and iodine substituents, makes it valuable in cross-coupling reactions, such as Suzuki and Sonogashira couplings, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. The presence of the iodine atom allows for easy functionalization, enabling the introduction of various other groups to the aromatic ring. Additionally, the fluorine atom can enhance the biological activity and metabolic stability of the final products, making it particularly useful in drug discovery and development. This compound is also employed in the synthesis of liquid crystals and organic electronic materials, where its unique electronic properties contribute to the desired performance characteristics.
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