(3-Oxo-2,3-dihydro-1H-inden-5-yl)boronic acid
95%
- Product Code: 220951
CAS:
1135871-83-8
| Molecular Weight: | 175.98 g./mol | Molecular Formula: | C₉H₉BO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22191954 | |
| Melting Point: | Boiling Point: | 396.2±52.0 °C(Predicted) | |
| Density: | 1.31±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid functionality allows for efficient coupling with aryl halides, making it valuable in constructing biaryl systems found in bioactive molecules. Commonly employed in the synthesis of indanone derivatives, which are structural motifs in medicinal chemistry for drug discovery targeting inflammation, cancer, and central nervous system disorders. Also utilized in materials science for creating conjugated organic frameworks with potential applications in optoelectronics.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿14,700.00 |
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| 1g | 10-20 days | ฿64,990.00 |
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(3-Oxo-2,3-dihydro-1H-inden-5-yl)boronic acid
Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid functionality allows for efficient coupling with aryl halides, making it valuable in constructing biaryl systems found in bioactive molecules. Commonly employed in the synthesis of indanone derivatives, which are structural motifs in medicinal chemistry for drug discovery targeting inflammation, cancer, and central nervous system disorders. Also utilized in materials science for creating conjugated organic frameworks with potential applications in optoelectronics.
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