2-fluoro-N-isopropyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
95%
- Product Code: 90602
CAS:
1689511-55-4
| Molecular Weight: | 307.1681232 g./mol | Molecular Formula: | C₁₆H₂₃BFNO₃ |
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| EC Number: | MDL Number: | MFCD31653840 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. The presence of the tetramethyl-1,3,2-dioxaborolane group makes it a valuable building block in Suzuki-Miyaura coupling reactions, which are widely used to form carbon-carbon bonds. Its application extends to the development of complex organic molecules, including those with potential therapeutic properties. Additionally, it is employed in the synthesis of boron-containing compounds, which are of interest in materials science and medicinal chemistry due to their unique properties and reactivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿9,612.00 |
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| 1.000 | 10-20 days | ฿28,080.00 |
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2-fluoro-N-isopropyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
This compound is primarily utilized in the field of organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. The presence of the tetramethyl-1,3,2-dioxaborolane group makes it a valuable building block in Suzuki-Miyaura coupling reactions, which are widely used to form carbon-carbon bonds. Its application extends to the development of complex organic molecules, including those with potential therapeutic properties. Additionally, it is employed in the synthesis of boron-containing compounds, which are of interest in materials science and medicinal chemistry due to their unique properties and reactivity.
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