(6-(Trifluoromethyl)pyridin-2-yl)boronic acid
95%
- Product Code: 49473
CAS:
1162257-61-5
Molecular Weight: | 190.9164 g./mol | Molecular Formula: | C₆H₅BF₃NO₂ |
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EC Number: | MDL Number: | MFCD08061586 | |
Melting Point: | Boiling Point: | 285.2±50.0 °C at 760 mmHg | |
Density: | 1.44±0.1 g/cm3 | Storage Condition: | -20℃, inert gas |
Product Description:
(6-(Trifluoromethyl)pyridin-2-yl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound’s trifluoromethyl group enhances its reactivity and stability, making it valuable in the development of biologically active compounds. It is also employed in the synthesis of heterocyclic compounds, which are crucial in drug discovery and material science. Additionally, its boronic acid functionality allows it to act as a key intermediate in the preparation of various functionalized pyridine derivatives.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.050 | 10-20 days | $86.23 |
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0.250 | 10-20 days | $287.42 |
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1.000 | 10-20 days | $701.64 |
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(6-(Trifluoromethyl)pyridin-2-yl)boronic acid
(6-(Trifluoromethyl)pyridin-2-yl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound’s trifluoromethyl group enhances its reactivity and stability, making it valuable in the development of biologically active compounds. It is also employed in the synthesis of heterocyclic compounds, which are crucial in drug discovery and material science. Additionally, its boronic acid functionality allows it to act as a key intermediate in the preparation of various functionalized pyridine derivatives.
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