(1-Oxo-2,3-dihydro-1H-inden-5-yl)boronic acid
98%
- Product Code: 220955
CAS:
221006-64-0
| Molecular Weight: | 175.97 g./mol | Molecular Formula: | C₉H₉BO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22414434 | |
| Melting Point: | Boiling Point: | 410.2±55.0 °C(Predicted) | |
| Density: | 1.31±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct biaryl compounds. Its boronic acid functionality allows for efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research for developing complex aromatic structures. The indanone-derived scaffold contributes to enhanced stability and reactivity in coupling processes. Commonly employed in the synthesis of bioactive molecules and functional materials where substituted indanone motifs are required.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | $145.26 |
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| 1g | 10-20 days | $558.70 |
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(1-Oxo-2,3-dihydro-1H-inden-5-yl)boronic acid
Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct biaryl compounds. Its boronic acid functionality allows for efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research for developing complex aromatic structures. The indanone-derived scaffold contributes to enhanced stability and reactivity in coupling processes. Commonly employed in the synthesis of bioactive molecules and functional materials where substituted indanone motifs are required.
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