N-(5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)acetamide
95%
- Product Code: 74415
CAS:
1201645-46-6
| Molecular Weight: | 262.11 g./mol | Molecular Formula: | C₁₃H₁₉BN₂O₃ |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry, where it serves as a key intermediate in the development of pharmaceutical agents. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in constructing complex molecules, including drug candidates and biologically active compounds. Additionally, the pyridine moiety in its structure enhances its potential in designing molecules with specific binding properties, making it useful in the development of targeted therapies. Its application extends to materials science, where it can be employed in the synthesis of organic electronic materials due to its ability to facilitate precise molecular modifications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿2,010.00 |
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| 0.100 | 10-20 days | ฿4,840.00 |
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N-(5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)acetamide
This compound is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry, where it serves as a key intermediate in the development of pharmaceutical agents. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in constructing complex molecules, including drug candidates and biologically active compounds. Additionally, the pyridine moiety in its structure enhances its potential in designing molecules with specific binding properties, making it useful in the development of targeted therapies. Its application extends to materials science, where it can be employed in the synthesis of organic electronic materials due to its ability to facilitate precise molecular modifications.
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