(5-((4-((tert-Butyldiphenylsilyl)oxy)piperidin-1-yl)sulfonyl)-2-methoxyphenyl)boronic aci
98%
- Product Code: 89329
CAS:
1704081-35-5
| Molecular Weight: | 553.5599999999999 g./mol | Molecular Formula: | C₂₈H₃₆BNO₆SSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28805772 | |
| 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 functional group enables it to act as a key intermediate in forming carbon-carbon bonds, which is essential in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyldiphenylsilyl (TBDPS) protecting group in its structure helps to stabilize the piperidinyl moiety during reactions, ensuring selective transformations. This chemical is often employed in the development of drug candidates, where precise functionalization of aromatic rings is required. Additionally, its sulfonyl group can enhance the reactivity and solubility of the compound, making it suitable for use in various catalytic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿42,100.00 |
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(5-((4-((tert-Butyldiphenylsilyl)oxy)piperidin-1-yl)sulfonyl)-2-methoxyphenyl)boronic aci
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables it to act as a key intermediate in forming carbon-carbon bonds, which is essential in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyldiphenylsilyl (TBDPS) protecting group in its structure helps to stabilize the piperidinyl moiety during reactions, ensuring selective transformations. This chemical is often employed in the development of drug candidates, where precise functionalization of aromatic rings is required. Additionally, its sulfonyl group can enhance the reactivity and solubility of the compound, making it suitable for use in various catalytic processes.
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