Methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate
95%
- Product Code: 209751
CAS:
1025718-91-5
| Molecular Weight: | 263.10 g./mol | Molecular Formula: | C₁₃H₁₈BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09027079 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used primarily in cross-coupling reactions, especially Suzuki-Miyaura coupling, to introduce the nicotinate ester moiety into complex organic molecules. This compound serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and functional materials where pyridine derivatives are required. Its boronate ester group enables efficient and selective bond formation under mild conditions, making it valuable in medicinal chemistry for constructing biaryl systems. It is also employed in the development of organic electronic materials due to the electron-deficient nature of the pyridine ring, which can influence charge transport properties.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿450.00 |
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| 1g | 10-20 days | ฿1,760.00 |
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| 5g | 10-20 days | ฿7,980.00 |
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| 25g | 10-20 days | ฿39,900.00 |
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Methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate
Used primarily in cross-coupling reactions, especially Suzuki-Miyaura coupling, to introduce the nicotinate ester moiety into complex organic molecules. This compound serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and functional materials where pyridine derivatives are required. Its boronate ester group enables efficient and selective bond formation under mild conditions, making it valuable in medicinal chemistry for constructing biaryl systems. It is also employed in the development of organic electronic materials due to the electron-deficient nature of the pyridine ring, which can influence charge transport properties.
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