4-(4-Ethylpiperazin-1-ylsulfonyl)phenylboronic acid
98%
- Product Code: 90448
CAS:
486422-70-2
| Molecular Weight: | 298.17 g./mol | Molecular Formula: | C₁₂H₁₉BN₂O₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26397905 | |
| 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. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, such as pharmaceuticals and agrochemicals. Its structure, featuring a sulfonyl group and an ethylpiperazine moiety, enhances its reactivity and selectivity in coupling reactions. Additionally, it is employed in the development of bioactive compounds and materials science, where it contributes to the creation of novel polymers and functional materials. Its stability and compatibility with various reaction conditions make it a valuable tool in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿18,620.00 |
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4-(4-Ethylpiperazin-1-ylsulfonyl)phenylboronic acid
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, such as pharmaceuticals and agrochemicals. Its structure, featuring a sulfonyl group and an ethylpiperazine moiety, enhances its reactivity and selectivity in coupling reactions. Additionally, it is employed in the development of bioactive compounds and materials science, where it contributes to the creation of novel polymers and functional materials. Its stability and compatibility with various reaction conditions make it a valuable tool in medicinal chemistry and drug discovery.
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