3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)picolinonitrile
97%
- Product Code: 244097
CAS:
878194-93-5
| Molecular Weight: | 230.07 g./mol | Molecular Formula: | C₁₂H₁₅BN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08458477 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry, inert gas |
Product Description:
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing for the formation of biaryl and heteroaryl structures commonly found in bioactive molecules. The nitrile group adds further functionality, enabling additional transformations such as hydrolysis to carboxylic acids or reduction to amines. It is especially valuable in medicinal chemistry for constructing complex nitrogen-containing heterocycles with high selectivity and yield.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $188.91 |
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| 1.000 | 10-20 days | $302.06 |
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| 5.000 | 10-20 days | $1,133.44 |
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3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)picolinonitrile
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing for the formation of biaryl and heteroaryl structures commonly found in bioactive molecules. The nitrile group adds further functionality, enabling additional transformations such as hydrolysis to carboxylic acids or reduction to amines. It is especially valuable in medicinal chemistry for constructing complex nitrogen-containing heterocycles with high selectivity and yield.
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