5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
97%
- Product Code: 240775
CAS:
269410-24-4
| Molecular Weight: | 243.11 g./mol | Molecular Formula: | C₁₄H₁₈BNO₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 120-125°C | Boiling Point: | 396°C |
| Density: | Storage Condition: | 2-8°C |
Product Description:
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds between aromatic systems. Its indole core makes it valuable in the construction of complex indole derivatives, which are common structural motifs in pharmaceuticals and natural products. The boronate ester group provides high stability and reactivity under mild conditions, allowing efficient coupling with aryl or heteroaryl halides. Frequently employed in drug discovery and development for generating libraries of biologically active compounds, especially in the design of serotonin receptor modulators and kinase inhibitors. Also applied in materials science for synthesizing conjugated organic molecules used in optoelectronic devices.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 250mg | 10-20 days | €3.79 |
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| 1g | 10-20 days | €18.45 |
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| 5g | 10-20 days | €58.24 |
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| 50g | 10-20 days | €517.84 |
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| 10g | 10-20 days | €110.16 |
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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds between aromatic systems. Its indole core makes it valuable in the construction of complex indole derivatives, which are common structural motifs in pharmaceuticals and natural products. The boronate ester group provides high stability and reactivity under mild conditions, allowing efficient coupling with aryl or heteroaryl halides. Frequently employed in drug discovery and development for generating libraries of biologically active compounds, especially in the design of serotonin receptor modulators and kinase inhibitors. Also applied in materials science for synthesizing conjugated organic molecules used in optoelectronic devices.
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