(4-Isopropoxy-3-(trifluoromethyl)phenyl)boronic acid
95%
- Product Code: 46525
CAS:
1444260-43-8
| Molecular Weight: | 248.01 g./mol | Molecular Formula: | C₁₀H₁₂BF₃O₃ |
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| EC Number: | MDL Number: | MFCD08059520 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
(4-Isopropoxy-3-(trifluoromethyl)phenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including biologically active compounds and drug candidates. Its boronic acid group enables efficient coupling with aryl halides or vinyl halides, facilitating the creation of diverse chemical structures. Additionally, its isopropoxy and trifluoromethyl substituents can enhance the stability and reactivity of the resulting products, making it a versatile reagent in medicinal chemistry and material science research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,596.00 |
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| 0.250 | 10-20 days | ฿12,672.00 |
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| 1.000 | 10-20 days | ฿33,822.00 |
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(4-Isopropoxy-3-(trifluoromethyl)phenyl)boronic acid
(4-Isopropoxy-3-(trifluoromethyl)phenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including biologically active compounds and drug candidates. Its boronic acid group enables efficient coupling with aryl halides or vinyl halides, facilitating the creation of diverse chemical structures. Additionally, its isopropoxy and trifluoromethyl substituents can enhance the stability and reactivity of the resulting products, making it a versatile reagent in medicinal chemistry and material science research.
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