Methyl 2-chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate
95%
- Product Code: 42918
CAS:
1622216-98-1
| Molecular Weight: | 297.54 g./mol | Molecular Formula: | C₁₃H₁₇BClNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16995192 | |
| Melting Point: | Boiling Point: | 396.5±42.0 °C at 760 mmHg | |
| Density: | 1.21±0.1 g/cm3 | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronate ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. This makes it valuable in the development of active pharmaceutical ingredients (APIs) and other fine chemicals. Additionally, it is utilized in research for designing and synthesizing novel compounds with potential biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $348.98 |
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| 0.250 | 10-20 days | $579.04 |
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| 1.000 | 10-20 days | $1,541.74 |
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Methyl 2-chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronate ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. This makes it valuable in the development of active pharmaceutical ingredients (APIs) and other fine chemicals. Additionally, it is utilized in research for designing and synthesizing novel compounds with potential biological activity.
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