2-methoxy-N-[3-(tetramethyl-1，3，2-dioxaborolan-2-yl)phenyl]acetamide
95%
- Product Code: 42174
CAS:
1853185-35-9
| Molecular Weight: | 291.15 g./mol | Molecular Formula: | C₁₅H₂₂BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31916416 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a tetramethyl dioxaborolane group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in complex molecules. Additionally, the methoxy and acetamide functionalities enhance its reactivity and selectivity in various chemical transformations, enabling the synthesis of biologically active compounds. Its application extends to materials science, where it contributes to the development of advanced polymers and organic electronic materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿3,672.00 |
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| 0.100 | 10-20 days | ฿10,998.00 |
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2-methoxy-N-[3-(tetramethyl-1，3，2-dioxaborolan-2-yl)phenyl]acetamide
This compound is primarily utilized in organic synthesis as a versatile intermediate, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a tetramethyl dioxaborolane group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in complex molecules. Additionally, the methoxy and acetamide functionalities enhance its reactivity and selectivity in various chemical transformations, enabling the synthesis of biologically active compounds. Its application extends to materials science, where it contributes to the development of advanced polymers and organic electronic materials.
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