N-Methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
95%
- Product Code: 215581
CAS:
1204742-77-7
| Molecular Weight: | 277.12 g./mol | Molecular Formula: | C₁₄H₂₀BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18383933 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.11±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions, allowing for the construction of biaryl and heterobiaryl systems. The N-methoxy amide moiety enhances stability and can act as a directing group or be further modified in multistep syntheses. Its structural features make it valuable in medicinal chemistry for building drug-like scaffolds with high functional group tolerance.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿1,200.00 |
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| 5g | 10-20 days | ฿3,800.00 |
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N-Methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions, allowing for the construction of biaryl and heterobiaryl systems. The N-methoxy amide moiety enhances stability and can act as a directing group or be further modified in multistep syntheses. Its structural features make it valuable in medicinal chemistry for building drug-like scaffolds with high functional group tolerance.
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