(5-(N-(tert-Butyl)sulfamoyl)pyridin-3-yl)boronic acid
95%
- Product Code: 37022
CAS:
1314987-50-2
| Molecular Weight: | 258.10 g./mol | Molecular Formula: | C₉H₁₅BN₂O₄S |
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| EC Number: | MDL Number: | MFCD27955970 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. It is often employed in the development of drug candidates, where it acts as a key intermediate in constructing biologically active compounds. Additionally, its pyridine ring structure provides stability and reactivity, enhancing its utility in medicinal chemistry and material science applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,974.00 |
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| 0.250 | 10-20 days | ฿13,302.00 |
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| 1.000 | 10-20 days | ฿35,352.00 |
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(5-(N-(tert-Butyl)sulfamoyl)pyridin-3-yl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. It is often employed in the development of drug candidates, where it acts as a key intermediate in constructing biologically active compounds. Additionally, its pyridine ring structure provides stability and reactivity, enhancing its utility in medicinal chemistry and material science applications.
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