2-(4-Methoxy-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
96%
- Product Code: 212192
CAS:
554411-20-0
| Molecular Weight: | 279.1 g./mol | Molecular Formula: | C₁₃H₁₈BNO₅ |
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| EC Number: | MDL Number: | MFCD06795663 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, 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 facilitates palladium-catalyzed coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl scaffolds. The methoxy and nitro substituents provide sites for further functionalization or act as directing groups in synthesis. Stable and easy to handle, it supports efficient and selective transformations in modern organic chemistry workflows.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿2,160.00 |
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| 1g | 10-20 days | ฿5,720.00 |
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| 5g | 10-20 days | ฿20,270.00 |
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| 10g | 10-20 days | ฿36,670.00 |
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2-(4-Methoxy-3-nitrophenyl)-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 facilitates palladium-catalyzed coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl scaffolds. The methoxy and nitro substituents provide sites for further functionalization or act as directing groups in synthesis. Stable and easy to handle, it supports efficient and selective transformations in modern organic chemistry workflows.
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