2-(2,6-Difluoro-3,5-dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
97%
- Product Code: 41287
CAS:
1614233-69-0
| Molecular Weight: | 300.1061 g./mol | Molecular Formula: | C₁₄H₁₉BF₂O₄ |
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| EC Number: | MDL Number: | MFCD30067285 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile boron-containing reagent. It plays a crucial role in cross-coupling reactions, particularly Suzuki-Miyaura coupling, which is widely employed in the formation of carbon-carbon bonds. Its stability and reactivity make it a valuable intermediate in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is used in the development of organic electronic materials due to its ability to facilitate the creation of conjugated systems. Its fluorine and methoxy substituents further enhance its utility in fine-tuning the electronic properties of target molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $233.60 |
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2-(2,6-Difluoro-3,5-dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This compound is primarily utilized in organic synthesis as a versatile boron-containing reagent. It plays a crucial role in cross-coupling reactions, particularly Suzuki-Miyaura coupling, which is widely employed in the formation of carbon-carbon bonds. Its stability and reactivity make it a valuable intermediate in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is used in the development of organic electronic materials due to its ability to facilitate the creation of conjugated systems. Its fluorine and methoxy substituents further enhance its utility in fine-tuning the electronic properties of target molecules.
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