1-Boc-6-methoxyindole-3-boronic acid pinacol ester
95%
- Product Code: 39718
CAS:
1256360-00-5
| Molecular Weight: | 373.25 g./mol | Molecular Formula: | C₂₀H₂₈BNO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14155740 | |
| Melting Point: | Boiling Point: | 485.6 °C at 760 mmHg | |
| Density: | Storage Condition: | -20℃, inert gas |
Product Description:
Used in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in pharmaceutical research. It is valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to construct indole derivatives. These derivatives are often explored for their potential biological activities, such as anticancer, anti-inflammatory, or antimicrobial properties. Additionally, it serves as a building block in the development of drug candidates targeting various diseases, leveraging the indole scaffold's versatility in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $352.51 |
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| 0.250 | 10-20 days | $663.18 |
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| 1.000 | 10-20 days | $1,631.95 |
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1-Boc-6-methoxyindole-3-boronic acid pinacol ester
Used in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in pharmaceutical research. It is valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to construct indole derivatives. These derivatives are often explored for their potential biological activities, such as anticancer, anti-inflammatory, or antimicrobial properties. Additionally, it serves as a building block in the development of drug candidates targeting various diseases, leveraging the indole scaffold's versatility in medicinal chemistry.
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