[4-(tert-butylcarbamoyl)-3-chloro-phenyl]boronic acid
97%
- Product Code: 242013
CAS:
850589-46-7
| Molecular Weight: | 255.5057 g./mol | Molecular Formula: | C₁₁H₁₅BClNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07363771 | |
| Melting Point: | 130-134 °C | Boiling Point: | |
| Density: | 1.24 g/cm3 | Storage Condition: | 2-8°C, dry |
Product Description:
Used in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. The presence of a tert-butylcarbamoyl group enhances stability and influences electronic properties, improving selectivity in coupling reactions. Commonly employed in the development of active pharmaceutical ingredients (APIs) where chloro-substituted aromatic systems are required as intermediates. Also utilized in materials science for constructing conjugated organic frameworks with tailored electronic characteristics.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | $44.87 |
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| 250mg | 10-20 days | $104.71 |
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| 1g | 10-20 days | $409.94 |
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[4-(tert-butylcarbamoyl)-3-chloro-phenyl]boronic acid
Used in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. The presence of a tert-butylcarbamoyl group enhances stability and influences electronic properties, improving selectivity in coupling reactions. Commonly employed in the development of active pharmaceutical ingredients (APIs) where chloro-substituted aromatic systems are required as intermediates. Also utilized in materials science for constructing conjugated organic frameworks with tailored electronic characteristics.
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