4-Bromo-1-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-indole
95%
- Product Code: 129903
CAS:
2247798-73-6
| Molecular Weight: | 336.03 g./mol | Molecular Formula: | C₁₅H₁₉BBrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16995792 | |
| Melting Point: | Boiling Point: | 436.0±25.0 °C(Predicted) | |
| Density: | 1.31±0.1 g/cm3(Predicted) | Storage Condition: | -20°C, Sealed, Inert Gas |
Product Description:
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex indole derivatives. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. Commonly applied in the development of bioactive molecules and functional materials where indole scaffolds are required. The presence of bromine and the boronate moiety allows for selective and sequential coupling reactions, enhancing synthetic versatility.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $625.90 |
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| 0.250 | 10-20 days | $234.71 |
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4-Bromo-1-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-indole
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex indole derivatives. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. Commonly applied in the development of bioactive molecules and functional materials where indole scaffolds are required. The presence of bromine and the boronate moiety allows for selective and sequential coupling reactions, enhancing synthetic versatility.
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