4-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
95%
- Product Code: 192683
CAS:
1072811-21-2
| Molecular Weight: | 273.14 g./mol | Molecular Formula: | C₁₅H₂₀BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11858387 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, Sealed, Inert Gas |
Product Description:
Used primarily as a key intermediate in pharmaceutical and agrochemical synthesis, this compound enables the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. Its boronate ester group facilitates mild and selective coupling with aryl or heteroaryl halides, making it valuable in constructing complex indole derivatives. These derivatives are commonly found in bioactive molecules, including drug candidates targeting inflammation, cancer, and neurological disorders. The methoxy group enhances electronic properties and stability, improving reaction efficiency and selectivity. It is also employed in materials science for developing organic semiconductors and fluorescent probes due to the indole core’s favorable photophysical characteristics.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 G | 10-20 days | ฿4,930.00 |
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| 1.000 G | 10-20 days | ฿13,300.00 |
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4-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
Used primarily as a key intermediate in pharmaceutical and agrochemical synthesis, this compound enables the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. Its boronate ester group facilitates mild and selective coupling with aryl or heteroaryl halides, making it valuable in constructing complex indole derivatives. These derivatives are commonly found in bioactive molecules, including drug candidates targeting inflammation, cancer, and neurological disorders. The methoxy group enhances electronic properties and stability, improving reaction efficiency and selectivity. It is also employed in materials science for developing organic semiconductors and fluorescent probes due to the indole core’s favorable photophysical characteristics.
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