(3-((Isopropoxycarbonyl)amino)phenyl)boronic acid
98%
- Product Code: 200767
CAS:
1638329-69-7
Molecular Weight: | 223.03 g./mol | Molecular Formula: | C₁₀H₁₄BNO₄ |
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EC Number: | MDL Number: | MFCD22375024 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Its boronic acid functionality allows it to react with aryl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical research for developing complex aromatic molecules. The isopropoxycarbonyl-protected amine group enhances stability and solubility during reaction processes, and can be deprotected to release the free amine for further functionalization. This compound is especially useful in medicinal chemistry for building drug-like scaffolds and bioactive molecules.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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100mg | 10-20 days | $55.19 |
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250mg | 10-20 days | $130.11 |
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5g | 10-20 days | $1,405.94 |
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1g | 10-20 days | $435.04 |
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(3-((Isopropoxycarbonyl)amino)phenyl)boronic acid
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Its boronic acid functionality allows it to react with aryl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical research for developing complex aromatic molecules. The isopropoxycarbonyl-protected amine group enhances stability and solubility during reaction processes, and can be deprotected to release the free amine for further functionalization. This compound is especially useful in medicinal chemistry for building drug-like scaffolds and bioactive molecules.
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