Imidodicarbonic acid, 2-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyrimidinyl]-, 1,3-bis(1,1-dimethylethyl) ester
≥95%
- Product Code: 200249
CAS:
1190423-36-9
| Molecular Weight: | 419.32 g./mol | Molecular Formula: | C₂₂H₃₄BNO₆ |
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| EC Number: | MDL Number: | MFCD12913985 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, stored in inert gas |
Product Description:
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester functionality allows for efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of protecting groups enhances stability and selectivity during reaction processes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 100mg | 10-20 days | $65.56 |
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| 250mg | 10-20 days | $94.57 |
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| 1g | 10-20 days | $236.43 |
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| 5g | 10-20 days | $787.17 |
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Imidodicarbonic acid, 2-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyrimidinyl]-, 1,3-bis(1,1-dimethylethyl) ester
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester functionality allows for efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of protecting groups enhances stability and selectivity during reaction processes.
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