(2-Fluoro-3-iodophenyl)boronic acid
97%
- Product Code: 67372
CAS:
1016231-39-2
| Molecular Weight: | 265.82 g./mol | Molecular Formula: | C₆H₅BFIO₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 238-243°C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
(2-Fluoro-3-iodophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound's unique structure, featuring both fluorine and iodine substituents, allows for selective functionalization, enabling the creation of complex molecules. It is also employed in the development of boron-based drugs and as a building block in medicinal chemistry for designing bioactive compounds. Additionally, its utility extends to material science, where it contributes to the synthesis of organic electronic materials and polymers.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | ฿288.00 |
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| 1.000 | 10-20 days | ฿648.00 |
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| 5.000 | 10-20 days | ฿2,637.00 |
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(2-Fluoro-3-iodophenyl)boronic acid
(2-Fluoro-3-iodophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound's unique structure, featuring both fluorine and iodine substituents, allows for selective functionalization, enabling the creation of complex molecules. It is also employed in the development of boron-based drugs and as a building block in medicinal chemistry for designing bioactive compounds. Additionally, its utility extends to material science, where it contributes to the synthesis of organic electronic materials and polymers.
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