N-(4-Chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide
98%
- Product Code: 219647
CAS:
1218789-92-4
| Molecular Weight: | 295.57 g./mol | Molecular Formula: | C₁₄H₁₉BClNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD15143594 | |
| Melting Point: | Boiling Point: | 454.6±40.0 °C at 760 mmHg | |
| Density: | 1.16±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, dry |
Product Description:
Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research for constructing biaryl scaffolds. The acetamide functionality can act as a directing or protecting group during transformations, enhancing selectivity. It is particularly useful in medicinal chemistry for building substituted aromatic systems found in bioactive compounds.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿2,630.00 |
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| 250mg | 10-20 days | ฿4,270.00 |
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| 1g | 10-20 days | ฿11,500.00 |
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| 5g | 10-20 days | ฿40,250.00 |
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N-(4-Chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide
Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research for constructing biaryl scaffolds. The acetamide functionality can act as a directing or protecting group during transformations, enhancing selectivity. It is particularly useful in medicinal chemistry for building substituted aromatic systems found in bioactive compounds.
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