1-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethanone
97%
- Product Code: 241546
CAS:
214360-49-3
| Molecular Weight: | 246.1099 g./mol | Molecular Formula: | C₁₄H₁₉BO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD05863923 | |
| Melting Point: | Boiling Point: | 362.5°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8℃ |
Product Description:
Used primarily in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable for constructing biaryl compounds commonly found in pharmaceuticals, agrochemicals, and advanced materials. The ketone functional group allows for further derivatization, such as reduction to alcohols or conversion to imines, enhancing its utility in multi-step synthesis. Commonly employed in the development of active pharmaceutical ingredients (APIs) and conjugated systems for optoelectronic materials.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $146.01 |
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| 10.000 | 10-20 days | $249.05 |
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1-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethanone
Used primarily in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable for constructing biaryl compounds commonly found in pharmaceuticals, agrochemicals, and advanced materials. The ketone functional group allows for further derivatization, such as reduction to alcohols or conversion to imines, enhancing its utility in multi-step synthesis. Commonly employed in the development of active pharmaceutical ingredients (APIs) and conjugated systems for optoelectronic materials.
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