2,3,4-Trifluoroiodobenzene
99%
- Product Code: 43795
CAS:
1190385-23-9
| Molecular Weight: | 257.9797596 g./mol | Molecular Formula: | C₆H₂F₃I |
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| Density: | Storage Condition: | room temperature |
Product Description:
2,3,4-Trifluoroiodobenzene is primarily used as a versatile building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring both fluorine and iodine atoms, makes it a valuable intermediate for introducing trifluoromethyl groups into more complex molecules, which are often sought after for their enhanced stability and biological activity. The compound is also employed in cross-coupling reactions, such as Suzuki and Sonogashira couplings, to create aromatic compounds with specific functional groups. Additionally, it serves as a precursor in the synthesis of liquid crystals and materials for electronic applications due to its ability to modify electronic properties. Its reactivity with various nucleophiles further expands its utility in creating diverse chemical structures for research and industrial purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $173.36 |
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| 25.000 | 10-20 days | $522.77 |
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| 100.000 | 10-20 days | $1,568.86 |
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2,3,4-Trifluoroiodobenzene
2,3,4-Trifluoroiodobenzene is primarily used as a versatile building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring both fluorine and iodine atoms, makes it a valuable intermediate for introducing trifluoromethyl groups into more complex molecules, which are often sought after for their enhanced stability and biological activity. The compound is also employed in cross-coupling reactions, such as Suzuki and Sonogashira couplings, to create aromatic compounds with specific functional groups. Additionally, it serves as a precursor in the synthesis of liquid crystals and materials for electronic applications due to its ability to modify electronic properties. Its reactivity with various nucleophiles further expands its utility in creating diverse chemical structures for research and industrial purposes.
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