tert-Butyl 3-formyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
98%
- Product Code: 118187
CAS:
1025707-92-9
| Molecular Weight: | 371.24 g./mol | Molecular Formula: | C₂₀H₂₆BNO₅ |
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| EC Number: | MDL Number: | MFCD07364063 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, inert gas |
Product Description:
This compound is primarily used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the construction of complex molecules, especially those involving indole derivatives. The presence of the formyl group and the boronate ester moiety makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. Additionally, its tert-butyl carboxylate group provides stability and facilitates selective deprotection in multi-step synthetic processes. This chemical is also employed in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Its versatility in functional group transformations makes it a valuable tool in medicinal chemistry and material science research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,971.00 |
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| 0.250 | 10-20 days | ฿3,339.00 |
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| 1.000 | 10-20 days | ฿9,000.00 |
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tert-Butyl 3-formyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
This compound is primarily used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the construction of complex molecules, especially those involving indole derivatives. The presence of the formyl group and the boronate ester moiety makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. Additionally, its tert-butyl carboxylate group provides stability and facilitates selective deprotection in multi-step synthetic processes. This chemical is also employed in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Its versatility in functional group transformations makes it a valuable tool in medicinal chemistry and material science research.
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