(3-(N-Isopropylsulfamoyl)-4-methoxyphenyl)boronic acid
98%
- Product Code: 65493
CAS:
874459-65-1
| Molecular Weight: | 273.12 g./mol | Molecular Formula: | C₁₀H₁₆BNO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400502 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and bioactive molecules. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds, which is essential in drug discovery and development. Additionally, the compound's structure, featuring an isopropylsulfamoyl group, makes it valuable in designing molecules with specific biological activities, particularly in targeting enzymes or receptors. It is also employed in the development of sensors and materials for detecting or binding specific analytes due to its boronic acid moiety's affinity for diols and other functional groups.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿40,920.00 |
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(3-(N-Isopropylsulfamoyl)-4-methoxyphenyl)boronic acid
Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and bioactive molecules. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds, which is essential in drug discovery and development. Additionally, the compound's structure, featuring an isopropylsulfamoyl group, makes it valuable in designing molecules with specific biological activities, particularly in targeting enzymes or receptors. It is also employed in the development of sensors and materials for detecting or binding specific analytes due to its boronic acid moiety's affinity for diols and other functional groups.
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