(1-(tert-Butoxycarbonyl)-6-cyano-1H-indol-2-yl)boronic acid
98%
- Product Code: 39716
CAS:
913835-67-3
Molecular Weight: | 286.0900 g./mol | Molecular Formula: | C₁₄H₁₅BN₂O₄ |
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EC Number: | MDL Number: | MFCD08436056 | |
Melting Point: | Boiling Point: | 509.1 °C at 760 mmHg | |
Density: | 1.21g/cm3 | Storage Condition: | -20°C |
Product Description:
This chemical is primarily used in organic synthesis, particularly in the preparation of complex molecules through cross-coupling reactions. It serves as a key intermediate in the development of pharmaceuticals, especially in the synthesis of indole-based compounds, which are important in drug discovery. The boronic acid group enables it to participate in Suzuki-Miyaura coupling reactions, a widely used method for forming carbon-carbon bonds. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthesis, making it valuable in the construction of biologically active molecules. Its applications are particularly relevant in the production of potential therapeutic agents targeting various diseases.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $100.16 |
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(1-(tert-Butoxycarbonyl)-6-cyano-1H-indol-2-yl)boronic acid
This chemical is primarily used in organic synthesis, particularly in the preparation of complex molecules through cross-coupling reactions. It serves as a key intermediate in the development of pharmaceuticals, especially in the synthesis of indole-based compounds, which are important in drug discovery. The boronic acid group enables it to participate in Suzuki-Miyaura coupling reactions, a widely used method for forming carbon-carbon bonds. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthesis, making it valuable in the construction of biologically active molecules. Its applications are particularly relevant in the production of potential therapeutic agents targeting various diseases.
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