(2-Methoxy-6-(trifluoromethyl)phenyl)boronic acid
≥95%
- Product Code: 113144
CAS:
1310384-19-0
| Molecular Weight: | 219.95 g./mol | Molecular Formula: | C₈H₈BF₃O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08059516 | |
| Melting Point: | Boiling Point: | 324.8°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
(2-Methoxy-6-(trifluoromethyl)phenyl)boronic acid is primarily utilized in organic synthesis as a key intermediate for the construction of complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. This reaction is widely employed in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs) and in materials science for creating advanced polymers and organic electronic materials. Additionally, its trifluoromethyl and methoxy substituents enhance its reactivity and stability, making it a versatile reagent in the development of agrochemicals and fine chemicals.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,718.00 |
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| 0.250 | 10-20 days | ฿4,770.00 |
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| 1.000 | 10-20 days | ฿10,692.00 |
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| 5.000 | 10-20 days | ฿44,253.00 |
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(2-Methoxy-6-(trifluoromethyl)phenyl)boronic acid
(2-Methoxy-6-(trifluoromethyl)phenyl)boronic acid is primarily utilized in organic synthesis as a key intermediate for the construction of complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. This reaction is widely employed in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs) and in materials science for creating advanced polymers and organic electronic materials. Additionally, its trifluoromethyl and methoxy substituents enhance its reactivity and stability, making it a versatile reagent in the development of agrochemicals and fine chemicals.
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