tert-Butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)piperidine-1-carboxylate
98%
blur_circular Chemical Specifications
description Product Description
Widely used in pharmaceutical synthesis, this compound serves as a key intermediate in cross-coupling reactions, particularly Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds. Its boronate ester group readily reacts with aryl or heteroaryl halides, making it valuable for constructing complex molecules in drug discovery. The piperidine and phenoxy groups provide structural motifs common in bioactive molecules, allowing incorporation into targets such as CNS agents, receptor modulators, or kinase inhibitors. The Boc-protected piperidine ensures compatibility with multi-step syntheses, offering a handle for deprotection and further functionalization. Its stability and reactivity profile make it suitable for high-throughput screening and parallel synthesis in medicinal chemistry.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance | White to pale-yellow to yellow-brown solid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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