(3-(4-((tert-Butyldimethylsilyl)oxy)piperidin-1-yl)-5-fluorophenyl)boronic acid
98%
- Product Code: 65475
CAS:
1704073-45-9
| Molecular Weight: | 353.32 g./mol | Molecular Formula: | C₁₇H₂₉BFNO₃Si |
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| EC Number: | MDL Number: | MFCD28384238 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyldimethylsilyl (TBDMS) protecting group on the piperidine moiety enhances its stability during reactions, allowing for selective deprotection and further functionalization. This compound is especially useful in medicinal chemistry for constructing biologically active molecules, including potential drug candidates targeting various diseases. Its fluorine substituent can influence the pharmacokinetic properties of the resulting compounds, such as metabolic stability and bioavailability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft540,860.22 |
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(3-(4-((tert-Butyldimethylsilyl)oxy)piperidin-1-yl)-5-fluorophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyldimethylsilyl (TBDMS) protecting group on the piperidine moiety enhances its stability during reactions, allowing for selective deprotection and further functionalization. This compound is especially useful in medicinal chemistry for constructing biologically active molecules, including potential drug candidates targeting various diseases. Its fluorine substituent can influence the pharmacokinetic properties of the resulting compounds, such as metabolic stability and bioavailability.
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