3,4,5-Trifluorophenylboronic acid
97%
- Product Code: 89907
Alias:
3,4,5-Trifluorophenylboronic acid
CAS:
143418-49-9
Molecular Weight: | 175.9 g./mol | Molecular Formula: | F₃C₆H₂BOH₂ |
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EC Number: | MDL Number: | MFCD02093069 | |
Melting Point: | 290-295 °C(lit.) | Boiling Point: | |
Density: | 1.087g/cm | Storage Condition: | room temperature |
Product Description:
3,4,5-Trifluorophenylboronic 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 creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its trifluorophenyl group enhances the reactivity and stability of the boronic acid, making it a valuable reagent in medicinal chemistry for drug discovery and development. Additionally, it serves as a building block in the synthesis of fluorinated compounds, which are often used in the production of active pharmaceutical ingredients (APIs) due to their unique properties, such as increased metabolic stability and bioavailability.
Product Specification:
Test | Specification |
---|---|
PURITYHPLC | 97 100% |
PURITYNEUTRALIZATION TITRATION | 96.5 100% |
APPEARANCE | White to brown powder |
INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿290.00 |
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5.000 | 10-20 days | ฿460.00 |
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25.000 | 10-20 days | ฿1,460.00 |
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100.000 | 10-20 days | ฿5,500.00 |
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3,4,5-Trifluorophenylboronic acid
3,4,5-Trifluorophenylboronic 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 creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its trifluorophenyl group enhances the reactivity and stability of the boronic acid, making it a valuable reagent in medicinal chemistry for drug discovery and development. Additionally, it serves as a building block in the synthesis of fluorinated compounds, which are often used in the production of active pharmaceutical ingredients (APIs) due to their unique properties, such as increased metabolic stability and bioavailability.
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