2-(3-Bromo-5-(cyclopropylmethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
- Product Code: 152406
CAS:
1218789-49-1
| Molecular Weight: | 353.06 g./mol | Molecular Formula: | C₁₆H₂₂BBrO₃ |
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| EC Number: | MDL Number: | MFCD12546588 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry |
Product Description:
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl systems. The presence of a bromo substituent allows for sequential functionalization, offering flexibility in multi-step syntheses. The cyclopropylmethoxy group contributes to electronic and steric properties that can influence reaction selectivity and biological activity in final compounds.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 50mg | 10-20 days | $53.25 |
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| 250mg | 10-20 days | $143.05 |
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2-(3-Bromo-5-(cyclopropylmethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl systems. The presence of a bromo substituent allows for sequential functionalization, offering flexibility in multi-step syntheses. The cyclopropylmethoxy group contributes to electronic and steric properties that can influence reaction selectivity and biological activity in final compounds.
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