(3-Fluoro-4-((4-methylpiperidin-1-yl)sulfonyl)phenyl)boronic aci
95%
- Product Code: 89107
CAS:
1704120-89-7
| Molecular Weight: | 301.15 g./mol | Molecular Formula: | C₁₂H₁₇BFNO₄S |
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| EC Number: | MDL Number: | MFCD28805565 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its unique structure, incorporating a fluoro and sulfonyl group, enhances its reactivity and selectivity in coupling reactions, allowing for the synthesis of complex molecules with high precision. It is also used in the development of bioactive compounds and as an intermediate in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿22,000.00 |
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| 0.250 | 10-20 days | ฿43,200.00 |
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| 1.000 | 10-20 days | ฿127,600.00 |
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(3-Fluoro-4-((4-methylpiperidin-1-yl)sulfonyl)phenyl)boronic aci
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its unique structure, incorporating a fluoro and sulfonyl group, enhances its reactivity and selectivity in coupling reactions, allowing for the synthesis of complex molecules with high precision. It is also used in the development of bioactive compounds and as an intermediate in medicinal chemistry research.
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