(3-(Pyrrolidin-1-yl)-5-(trifluoromethyl)phenyl)boronic acid
98%
- Product Code: 65512
CAS:
1704067-30-0
| Molecular Weight: | 259.04 g./mol | Molecular Formula: | C₁₁H₁₃BF₃NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384240 | |
| 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 building block for the introduction of the trifluoromethylphenyl group into various organic molecules, which is valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The trifluoromethyl group enhances the biological activity and metabolic stability of the resulting compounds, making it useful in drug discovery and medicinal chemistry. Additionally, its boronic acid functionality allows for precise and efficient coupling with aryl halides, enabling the creation of complex molecular architectures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | $1,205.10 |
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(3-(Pyrrolidin-1-yl)-5-(trifluoromethyl)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 building block for the introduction of the trifluoromethylphenyl group into various organic molecules, which is valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The trifluoromethyl group enhances the biological activity and metabolic stability of the resulting compounds, making it useful in drug discovery and medicinal chemistry. Additionally, its boronic acid functionality allows for precise and efficient coupling with aryl halides, enabling the creation of complex molecular architectures.
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