2-Methoxy-3-(trifluoromethyl)pyridine-5-boronic Acid Pinacol Ester
95%
- Product Code: 89842
CAS:
1150561-61-7
| Molecular Weight: | 303.09 g./mol | Molecular Formula: | C₁₃H₁₇F₃NO₃B |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12026094 | |
| 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 versatile building block for introducing the 2-methoxy-3-(trifluoromethyl)pyridine moiety into more complex molecules. Its stability and reactivity make it valuable in pharmaceutical research, where it is used to develop novel drug candidates, especially those targeting neurological and inflammatory diseases. Additionally, it finds applications in agrochemical synthesis for creating compounds with enhanced biological activity. Its trifluoromethyl group contributes to improved metabolic stability and bioavailability in the final products.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $828.63 |
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| 5.000 | 10-20 days | $2,538.96 |
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2-Methoxy-3-(trifluoromethyl)pyridine-5-boronic Acid Pinacol Ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile building block for introducing the 2-methoxy-3-(trifluoromethyl)pyridine moiety into more complex molecules. Its stability and reactivity make it valuable in pharmaceutical research, where it is used to develop novel drug candidates, especially those targeting neurological and inflammatory diseases. Additionally, it finds applications in agrochemical synthesis for creating compounds with enhanced biological activity. Its trifluoromethyl group contributes to improved metabolic stability and bioavailability in the final products.
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