(3-(N-Isopropyl-N-(4-methoxybenzyl)sulfamoyl)phenyl)boronic acid
96%
- Product Code: 87071
CAS:
1217501-23-9
| Molecular Weight: | 363.24 g./mol | Molecular Formula: | C₁₇H₂₂BNO₅S |
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| EC Number: | MDL Number: | MFCD12756420 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a boronic acid derivative, enabling the formation of carbon-carbon bonds, which is crucial in constructing complex organic molecules. Its structure, featuring a sulfamoyl group and a methoxybenzyl moiety, enhances its reactivity and selectivity in these reactions. Additionally, it finds application in the development of pharmaceuticals, where it serves as an intermediate in the synthesis of biologically active compounds. Its unique properties also make it valuable in material science for creating advanced polymers and functional materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,971.00 |
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| 0.250 | 10-20 days | ฿3,339.00 |
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| 1.000 | 10-20 days | ฿9,000.00 |
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(3-(N-Isopropyl-N-(4-methoxybenzyl)sulfamoyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a boronic acid derivative, enabling the formation of carbon-carbon bonds, which is crucial in constructing complex organic molecules. Its structure, featuring a sulfamoyl group and a methoxybenzyl moiety, enhances its reactivity and selectivity in these reactions. Additionally, it finds application in the development of pharmaceuticals, where it serves as an intermediate in the synthesis of biologically active compounds. Its unique properties also make it valuable in material science for creating advanced polymers and functional materials.
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