2-(3-Methoxy-5-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
97%
- Product Code: 115694
CAS:
479411-93-3
| Molecular Weight: | 302.10 g./mol | Molecular Formula: | C₁₄H₁₈BF₃O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11846463 | |
| Melting Point: | Boiling Point: | 340.4±42.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its trifluoromethyl and methoxy groups enhance its reactivity and selectivity, making it valuable in the synthesis of complex organic molecules. Additionally, it is employed in the preparation of bioactive compounds and intermediates for drug discovery, contributing to the development of new therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,241.00 |
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| 5.000 | 10-20 days | ฿9,108.00 |
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| 10.000 | 10-20 days | ฿15,291.00 |
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2-(3-Methoxy-5-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its trifluoromethyl and methoxy groups enhance its reactivity and selectivity, making it valuable in the synthesis of complex organic molecules. Additionally, it is employed in the preparation of bioactive compounds and intermediates for drug discovery, contributing to the development of new therapeutic agents.
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