1-Boc-6-methylindole-3-boronic acid pinacol ester
95%
- Product Code: 39717
CAS:
1256359-86-0
| Molecular Weight: | 375.27 g./mol | Molecular Formula: | C₂₀H₃₀BNO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16295108 | |
| Melting Point: | Boiling Point: | 469.6 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8℃, dry, airtight |
Product Description:
This compound is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a key building block for constructing complex molecules. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The Boc (tert-butoxycarbonyl) protecting group enhances its stability during reactions and allows for selective deprotection when needed. Additionally, its indole core is significant in the synthesis of biologically active compounds, including drug candidates targeting various diseases. Its application extends to the development of organic electronic materials due to the unique properties of the indole moiety.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $247.71 |
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| 1.000 | 10-20 days | $495.88 |
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| 5.000 | 10-20 days | $1,487.64 |
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1-Boc-6-methylindole-3-boronic acid pinacol ester
This compound is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a key building block for constructing complex molecules. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The Boc (tert-butoxycarbonyl) protecting group enhances its stability during reactions and allows for selective deprotection when needed. Additionally, its indole core is significant in the synthesis of biologically active compounds, including drug candidates targeting various diseases. Its application extends to the development of organic electronic materials due to the unique properties of the indole moiety.
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