N-Methyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide
98%
- Product Code: 219558
CAS:
1256359-34-8
| Molecular Weight: | 275.15 g./mol | Molecular Formula: | C₁₅H₂₂BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16660303 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its boron-containing group enables the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and functional materials. The presence of the acetamide moiety can act as a directing group or contribute to biological activity in drug discovery intermediates. It is especially useful for constructing biaryl structures under palladium catalysis. Its stability and reactivity profile make it suitable for late-stage functionalization in complex molecule synthesis.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿2,630.00 |
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| 250mg | 10-20 days | ฿4,450.00 |
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| 1g | 10-20 days | ฿11,500.00 |
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| 5g | 10-20 days | ฿40,250.00 |
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N-Methyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide
Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its boron-containing group enables the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and functional materials. The presence of the acetamide moiety can act as a directing group or contribute to biological activity in drug discovery intermediates. It is especially useful for constructing biaryl structures under palladium catalysis. Its stability and reactivity profile make it suitable for late-stage functionalization in complex molecule synthesis.
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