(4-(((1-(tert-butoxycarbonyl)piperidin-4-yl)oxy)methyl)phenyl)boronic acid (4-(((1-(tert-Butoxycarbonyl)piperidin-4-yl)oxy)methyl)phenyl)boronic acid
98%
- Product Code: 89168
CAS:
1224449-13-1
| Molecular Weight: | 335.21 g./mol | Molecular Formula: | C₁₇H₂₆BNO₅ |
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| EC Number: | MDL Number: | MFCD28400568 | |
| 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. It serves as a boronic acid derivative, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protected piperidine moiety, makes it valuable in medicinal chemistry for the development of drug candidates. The Boc group provides stability during synthetic processes, while the boronic acid functionality allows for versatile coupling with aryl or vinyl halides. This compound is often employed in the preparation of biologically active molecules, including pharmaceuticals and agrochemicals, where precise control over molecular architecture is essential. Additionally, its application extends to materials science, where it contributes to the design of advanced organic materials with tailored properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿11,430.00 |
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(4-(((1-(tert-butoxycarbonyl)piperidin-4-yl)oxy)methyl)phenyl)boronic acid (4-(((1-(tert-Butoxycarbonyl)piperidin-4-yl)oxy)methyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid derivative, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protected piperidine moiety, makes it valuable in medicinal chemistry for the development of drug candidates. The Boc group provides stability during synthetic processes, while the boronic acid functionality allows for versatile coupling with aryl or vinyl halides. This compound is often employed in the preparation of biologically active molecules, including pharmaceuticals and agrochemicals, where precise control over molecular architecture is essential. Additionally, its application extends to materials science, where it contributes to the design of advanced organic materials with tailored properties.
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