(4-(N-Cyclopentylsulfamoyl)-3, 5-dimethylphenyl)boronic acid
98%
- Product Code: 89269
CAS:
1704097-46-0
| Molecular Weight: | 297.18 g./mol | Molecular Formula: | C₁₃H₂₀BNO₄S |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It acts 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 cyclopentylsulfamoyl group, may contribute to enhanced stability or selectivity in certain reactions. Additionally, it can be employed in the development of bioactive compounds or as an intermediate in the preparation of advanced materials. Its application is often tailored to specific research or industrial needs, particularly in fields requiring precise molecular construction.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $1,859.25 |
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(4-(N-Cyclopentylsulfamoyl)-3, 5-dimethylphenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It acts 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 cyclopentylsulfamoyl group, may contribute to enhanced stability or selectivity in certain reactions. Additionally, it can be employed in the development of bioactive compounds or as an intermediate in the preparation of advanced materials. Its application is often tailored to specific research or industrial needs, particularly in fields requiring precise molecular construction.
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