(1-(tert-Butoxycarbonyl)-6-(methoxycarbonyl)-1H-indol-2-yl)boronic acid
98%
- Product Code: 117002
CAS:
848357-46-0
| Molecular Weight: | 319.12 g./mol | Molecular Formula: | C₁₅H₁₈BNO₆ |
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| EC Number: | MDL Number: | MFCD11616319 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the construction of complex molecules. It serves as a key intermediate in the development of pharmaceuticals, especially in the synthesis of indole-based compounds. The boronic acid moiety enables its use in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This makes it valuable in the production of biologically active molecules, including potential drug candidates. Additionally, its tert-butoxycarbonyl (Boc) and methoxycarbonyl protecting groups enhance its stability and reactivity during multi-step synthetic processes, allowing for precise modifications in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $322.56 |
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(1-(tert-Butoxycarbonyl)-6-(methoxycarbonyl)-1H-indol-2-yl)boronic acid
This chemical is primarily utilized in organic synthesis, particularly in the construction of complex molecules. It serves as a key intermediate in the development of pharmaceuticals, especially in the synthesis of indole-based compounds. The boronic acid moiety enables its use in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This makes it valuable in the production of biologically active molecules, including potential drug candidates. Additionally, its tert-butoxycarbonyl (Boc) and methoxycarbonyl protecting groups enhance its stability and reactivity during multi-step synthetic processes, allowing for precise modifications in medicinal chemistry research.
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