(1-(tert-Butoxycarbonyl)-1,2,3,6-tetrahydropyridin-4-yl)boronic acid
97%
science Other reagents with same CAS 844501-00-4
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description Product Description
This compound is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry, where it serves as a key intermediate in the development of pharmaceutical agents. Its boronic acid group makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in constructing complex molecules, including bioactive compounds and drug candidates. Additionally, the tert-butoxycarbonyl (Boc) protecting group enhances its stability and facilitates selective reactions, making it a versatile building block in multi-step synthetic processes. Its applications extend to the synthesis of heterocyclic compounds, which are often found in drugs targeting various diseases.
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| Test Parameter | Specification |
|---|---|
| APPEARANCE | White to Off-white to Pale yellow to Yellow Solid |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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