1-Ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
97%
- Product Code: 183522
CAS:
1219741-53-3
| Molecular Weight: | 271.16 g./mol | Molecular Formula: | C₁₆H₂₂BNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18383812 | |
| Melting Point: | Boiling Point: | 380.9°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, stored in inert gas |
Product Description:
Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. It enables the formation of carbon-carbon bonds, particularly in the construction of biaryl or aryl-heteroaryl frameworks found in pharmaceuticals and agrochemicals. The indole moiety makes it valuable for synthesizing bioactive molecules, including drug candidates targeting neurological disorders, inflammation, and cancer. Its boronate ester group offers stability and reactivity under palladium catalysis, making it suitable for late-stage functionalization in complex molecule assembly. Commonly employed in medicinal chemistry and materials science for building nitrogen-containing aromatic systems with tailored electronic properties.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | $71.08 |
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| 250mg | 10-20 days | $122.54 |
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1-Ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. It enables the formation of carbon-carbon bonds, particularly in the construction of biaryl or aryl-heteroaryl frameworks found in pharmaceuticals and agrochemicals. The indole moiety makes it valuable for synthesizing bioactive molecules, including drug candidates targeting neurological disorders, inflammation, and cancer. Its boronate ester group offers stability and reactivity under palladium catalysis, making it suitable for late-stage functionalization in complex molecule assembly. Commonly employed in medicinal chemistry and materials science for building nitrogen-containing aromatic systems with tailored electronic properties.
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