(5-(N-Cyclohexylsulfamoyl)-2-methoxyphenyl)boronic acid
98%
- Product Code: 89342
CAS:
1704081-61-7
| Molecular Weight: | 313.18 g./mol | Molecular Formula: | C₁₃H₂₀BNO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400437 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. It facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its structure, featuring a cyclohexylsulfamoyl group and a methoxy substituent, enhances its stability and reactivity in these reactions. Additionally, it is employed in the development of bioactive compounds and as a building block in medicinal chemistry for designing potential drug candidates. Its utility in synthesizing complex organic molecules underscores its importance in research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿42,100.00 |
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(5-(N-Cyclohexylsulfamoyl)-2-methoxyphenyl)boronic acid
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. It facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its structure, featuring a cyclohexylsulfamoyl group and a methoxy substituent, enhances its stability and reactivity in these reactions. Additionally, it is employed in the development of bioactive compounds and as a building block in medicinal chemistry for designing potential drug candidates. Its utility in synthesizing complex organic molecules underscores its importance in research and industrial applications.
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