9-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinoline
≥98%
- Product Code: 238167
CAS:
1262331-13-4
Molecular Weight: | 299.22 g./mol | Molecular Formula: | C₁₈H₂₆BNO₂ |
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EC Number: | MDL Number: | MFCD30737792 | |
Melting Point: | Boiling Point: | 462.1±44.0 °C(Predicted) | |
Density: | 1.10±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or heteroaryl halides, making it valuable in pharmaceutical and agrochemical research. It is particularly useful in constructing polycyclic and nitrogen-containing frameworks found in bioactive compounds. The rigid, fused ring structure enhances selectivity and stability during reactions, improving yields in target molecule assembly.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿10,010.00 |
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1.000 | 10-20 days | ฿41,500.00 |
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9-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinoline
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or heteroaryl halides, making it valuable in pharmaceutical and agrochemical research. It is particularly useful in constructing polycyclic and nitrogen-containing frameworks found in bioactive compounds. The rigid, fused ring structure enhances selectivity and stability during reactions, improving yields in target molecule assembly.
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