2-(Cyclopropylmethoxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
95%
- Product Code: 61039
CAS:
947191-69-7
| Molecular Weight: | 275.15 g./mol | Molecular Formula: | C₁₅H₂₂BNO₃ |
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| EC Number: | MDL Number: | MFCD07781184 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable reagent for forming carbon-carbon bonds, which is essential in the construction of complex organic molecules. It is often employed in the pharmaceutical industry for the development of drug candidates, enabling the introduction of pyridine and cyclopropylmethoxy moieties into target molecules. Additionally, it serves as a key intermediate in the synthesis of agrochemicals and materials science applications, where precise molecular architecture is required. Its stability and reactivity under mild conditions make it a preferred choice for chemists working on advanced synthetic routes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿1,017.00 |
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| 0.250 | 10-20 days | ฿3,096.00 |
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2-(Cyclopropylmethoxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable reagent for forming carbon-carbon bonds, which is essential in the construction of complex organic molecules. It is often employed in the pharmaceutical industry for the development of drug candidates, enabling the introduction of pyridine and cyclopropylmethoxy moieties into target molecules. Additionally, it serves as a key intermediate in the synthesis of agrochemicals and materials science applications, where precise molecular architecture is required. Its stability and reactivity under mild conditions make it a preferred choice for chemists working on advanced synthetic routes.
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