N-(2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)methanesulfonamide
≥95%
- Product Code: 121333
CAS:
1083326-75-3
| Molecular Weight: | 328.19 g./mol | Molecular Formula: | C₁₃H₂₁BN₂O₅S |
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| EC Number: | MDL Number: | MFCD12964555 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. It is often employed in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Additionally, it serves as a building block in material science for creating advanced polymers and organic electronic materials. Its stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,887.00 |
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| 0.250 | 10-20 days | ฿9,270.00 |
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| 1.000 | 10-20 days | ฿22,608.00 |
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N-(2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)methanesulfonamide
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. It is often employed in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Additionally, it serves as a building block in material science for creating advanced polymers and organic electronic materials. Its stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.
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