Potassium trifluoro(4-methoxybenzyl)borate
97%
- Product Code: 227657
CAS:
900810-91-5
| Molecular Weight: | 228.06 g./mol | Molecular Formula: | C₈H₉F₃OBK |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09993297 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, Inert Gas |
Product Description:
Used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a stable boron-containing partner that enables the formation of carbon-carbon bonds, especially in the synthesis of biaryl compounds. The 4-methoxybenzyl group enhances reactivity and selectivity in certain coupling processes, making it valuable in pharmaceutical and agrochemical research where complex aromatic structures are common. Its potassium and trifluoroborate components contribute to improved solubility and handling compared to other boronic acid derivatives.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,200.00 |
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| 1.000 | 10-20 days | ฿13,030.00 |
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| 5.000 | 10-20 days | ฿56,630.00 |
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| 0.250 | 10-20 days | ฿3,270.00 |
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Potassium trifluoro(4-methoxybenzyl)borate
Used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a stable boron-containing partner that enables the formation of carbon-carbon bonds, especially in the synthesis of biaryl compounds. The 4-methoxybenzyl group enhances reactivity and selectivity in certain coupling processes, making it valuable in pharmaceutical and agrochemical research where complex aromatic structures are common. Its potassium and trifluoroborate components contribute to improved solubility and handling compared to other boronic acid derivatives.
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