2-methyl-1-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethylpiperidine
95%
- Product Code: 209506
CAS:
2246419-29-2
| Molecular Weight: | 345.28398 g./mol | Molecular Formula: | C₂₀H₃₂BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32206515 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
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 group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable for constructing complex organic molecules. It is especially useful in the development of bioactive compounds and functional materials where precise molecular architecture is required. The presence of the piperidine and ether functionalities allows for further derivatization, enhancing its utility in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿22,080.00 |
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| 1g | 10-20 days | ฿48,000.00 |
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2-methyl-1-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethylpiperidine
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 group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable for constructing complex organic molecules. It is especially useful in the development of bioactive compounds and functional materials where precise molecular architecture is required. The presence of the piperidine and ether functionalities allows for further derivatization, enhancing its utility in medicinal chemistry and drug discovery.
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