(3-Chloro-4-(2-(4-methylpiperidin-1-yl)ethoxy)phenyl)boronic acid
98%
- Product Code: 89133
CAS:
1704074-00-9
| Molecular Weight: | 297.59 g./mol | Molecular Formula: | C₁₄H₂₁BClNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384316 | |
| 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 key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of drugs targeting various diseases, as well as in the synthesis of advanced materials. Additionally, its structural features may contribute to its use in designing compounds with specific biological activities, such as enzyme inhibitors or receptor modulators.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿51,810.00 |
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(3-Chloro-4-(2-(4-methylpiperidin-1-yl)ethoxy)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 key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of drugs targeting various diseases, as well as in the synthesis of advanced materials. Additionally, its structural features may contribute to its use in designing compounds with specific biological activities, such as enzyme inhibitors or receptor modulators.
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