2-(4-Methylpiperidin-1-yl)-5-(trifluoromethyl)phenylboronic acid
98%
- Product Code: 89636
CAS:
1704063-77-3
| Molecular Weight: | 287.09 g./mol | Molecular Formula: | C₁₃H₁₇BF₃NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384245 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. Its trifluoromethyl group enhances reactivity and stability, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is employed in material science for creating advanced polymers and functional materials with specific properties. Its unique structure allows for precise modifications in target molecules, contributing to innovations in medicinal chemistry and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿21,660.00 |
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2-(4-Methylpiperidin-1-yl)-5-(trifluoromethyl)phenylboronic acid
This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. Its trifluoromethyl group enhances reactivity and stability, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is employed in material science for creating advanced polymers and functional materials with specific properties. Its unique structure allows for precise modifications in target molecules, contributing to innovations in medicinal chemistry and industrial applications.
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