N-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methacrylamide
98%
- Product Code: 218031
CAS:
1056904-42-7
| Molecular Weight: | 287.16178 g./mol | Molecular Formula: | C₁₆H₂₂BNO₃ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 448.5±37.0℃ at 760 mmHg | |
| Density: | 1.06±0.1 g/cm3 | Storage Condition: | Room temperature, sealed, dry |
Product Description:
Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of functionalized amides and conjugated polymers. Its boronate ester group enables efficient carbon-carbon bond formation under palladium catalysis, making it valuable in pharmaceutical development and materials science. The methacrylamide functionality allows for subsequent radical polymerization, enabling the creation of stimuli-responsive polymers and functional coatings. It is also employed in the preparation of boron-containing organic frameworks for sensing and catalytic applications.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 250mg | 10-20 days | £29.15 |
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| 1g | 10-20 days | £79.42 |
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| 5g | 10-20 days | £328.26 |
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N-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methacrylamide
Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of functionalized amides and conjugated polymers. Its boronate ester group enables efficient carbon-carbon bond formation under palladium catalysis, making it valuable in pharmaceutical development and materials science. The methacrylamide functionality allows for subsequent radical polymerization, enabling the creation of stimuli-responsive polymers and functional coatings. It is also employed in the preparation of boron-containing organic frameworks for sensing and catalytic applications.
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