1-(tert-Butyl) 4-methyl 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1,4-dicarboxylate
97%
- Product Code: 192508
CAS:
2377607-84-4
| Molecular Weight: | 401.26 g./mol | Molecular Formula: | C₂₁H₂₈BNO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28101648 | |
| Melting Point: | Boiling Point: | 519.2±60.0 °C(Predicted) | |
| Density: | 1.14±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Used primarily as a key intermediate in pharmaceutical and agrochemical synthesis, this compound enables the formation of complex indole derivatives through Suzuki-Miyaura cross-coupling reactions. Its boronate ester functionality allows for efficient carbon-carbon bond formation, making it valuable in the development of bioactive molecules and functional materials. The tert-butyl and methyl protecting groups enhance stability and selectivity during multi-step syntheses, particularly in the construction of drug-like scaffolds. It is especially useful in research settings for generating novel indole-based compounds with potential therapeutic activity.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 G | 10-20 days | ฿12,000.00 |
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| 0.250 G | 10-20 days | ฿4,500.00 |
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1-(tert-Butyl) 4-methyl 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1,4-dicarboxylate
Used primarily as a key intermediate in pharmaceutical and agrochemical synthesis, this compound enables the formation of complex indole derivatives through Suzuki-Miyaura cross-coupling reactions. Its boronate ester functionality allows for efficient carbon-carbon bond formation, making it valuable in the development of bioactive molecules and functional materials. The tert-butyl and methyl protecting groups enhance stability and selectivity during multi-step syntheses, particularly in the construction of drug-like scaffolds. It is especially useful in research settings for generating novel indole-based compounds with potential therapeutic activity.
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