Pinacol 2-chloro-3-methoxypyridine-5-borate
95%
- Product Code: 42855
CAS:
1256360-28-7
| Molecular Weight: | 269.53 g./mol | Molecular Formula: | C₁₂H₁₇BClNO₃ |
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| EC Number: | MDL Number: | MFCD16660309 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃, dry, airtight |
Product Description:
Pinacol 2-chloro-3-methoxypyridine-5-borate is primarily utilized in organic synthesis as a versatile building block for the creation of complex molecules. Its borate ester functionality makes it a valuable reagent in cross-coupling reactions, particularly Suzuki-Miyaura couplings, where it facilitates the formation of carbon-carbon bonds. This compound is also employed in the development of pharmaceuticals and agrochemicals, where its unique structure allows for the introduction of specific functional groups into target molecules. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry for designing drugs with enhanced biological activity. Its stability and reactivity make it a preferred choice in research and industrial applications for constructing diverse chemical architectures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $148.51 |
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| 0.250 | 10-20 days | $247.88 |
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| 1.000 | 10-20 days | $661.03 |
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Pinacol 2-chloro-3-methoxypyridine-5-borate
Pinacol 2-chloro-3-methoxypyridine-5-borate is primarily utilized in organic synthesis as a versatile building block for the creation of complex molecules. Its borate ester functionality makes it a valuable reagent in cross-coupling reactions, particularly Suzuki-Miyaura couplings, where it facilitates the formation of carbon-carbon bonds. This compound is also employed in the development of pharmaceuticals and agrochemicals, where its unique structure allows for the introduction of specific functional groups into target molecules. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry for designing drugs with enhanced biological activity. Its stability and reactivity make it a preferred choice in research and industrial applications for constructing diverse chemical architectures.
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