6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoxaline
95%
Reagent
Code: #241729
CAS Number
1167418-13-4
blur_circular Chemical Specifications
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Molecular Information
Weight
256.11 g/mol
Formula
C₁₄H₁₇BN₂O₂
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Registry Numbers
MDL Number
MFCD11054040
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Storage & Handling
Storage
2-8°C, stored in inert gas
description Product Description
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl and heteroaryl frameworks common in pharmaceuticals and functional materials. Its quinoxaline core acts as an electron-deficient aromatic system, making it valuable in the development of organic semiconductors, sensors, and luminescent materials. Also employed as a building block in medicinal chemistry for designing kinase inhibitors and other bioactive compounds due to the quinoxaline moiety’s biological activity. The boronate ester group allows for efficient and selective carbon-carbon bond formation under mild conditions, enhancing its utility in drug discovery and materials science.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance | Colorless to yellow to yellow-brown liquid or solid |
| Purity (%) | 94.5-100% |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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