(4-(2-(4-((tert-Butyldiphenylsilyl)oxy)piperidin-1-yl)ethoxy)-3-chlorophenyl)boronic acid
98%
- Product Code: 89232
CAS:
1704074-62-3
| Molecular Weight: | 537.97 g./mol | Molecular Formula: | C₂₉H₃₇BClNO₄Si |
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| EC Number: | MDL Number: | MFCD28805757 | |
| 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 the Suzuki-Miyaura reaction. Its boronic acid group enables it to act as a key reagent in forming carbon-carbon bonds, which is essential in constructing complex organic molecules. The tert-butyldiphenylsilyl (TBDPS) protecting group enhances its stability and selectivity during these reactions, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its piperidine moiety contributes to its potential application in medicinal chemistry, where it may be used to develop bioactive compounds targeting specific receptors or enzymes. Its chloro substituent further allows for additional functionalization, expanding its utility in diverse chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | $1,371.82 |
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(4-(2-(4-((tert-Butyldiphenylsilyl)oxy)piperidin-1-yl)ethoxy)-3-chlorophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables it to act as a key reagent in forming carbon-carbon bonds, which is essential in constructing complex organic molecules. The tert-butyldiphenylsilyl (TBDPS) protecting group enhances its stability and selectivity during these reactions, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its piperidine moiety contributes to its potential application in medicinal chemistry, where it may be used to develop bioactive compounds targeting specific receptors or enzymes. Its chloro substituent further allows for additional functionalization, expanding its utility in diverse chemical transformations.
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