(3-(N,N-Dimethylsulfamoyl)-4-methoxyphenyl)boronic acid
95%
- Product Code: 65486
CAS:
874459-70-8
| Molecular Weight: | 259.09 g./mol | Molecular Formula: | C₉H₁₄BNO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400499 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its structure, featuring a sulfamoyl group and a methoxy substituent, enhances its reactivity and selectivity in these reactions. Additionally, it is employed in the development of bioactive compounds and materials science, where its unique properties contribute to the creation of advanced polymers and functional materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿15,290.00 |
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| 0.100 | 10-20 days | ฿46,690.00 |
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(3-(N,N-Dimethylsulfamoyl)-4-methoxyphenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its structure, featuring a sulfamoyl group and a methoxy substituent, enhances its reactivity and selectivity in these reactions. Additionally, it is employed in the development of bioactive compounds and materials science, where its unique properties contribute to the creation of advanced polymers and functional materials.
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