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*For research and further manufacturing use only, not for direct human use.
Structure of 2058236-52-3
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(S)-Bn-iQuinox delivers a chiral, bench-stable scaffold for asymmetric synthesis, featuring a protected amino group and a quinoxaline core that enables efficient coupling reactions. This rigid, electron-deficient heterocycle facilitates stereocontrolled transformations in medicinal chemistry and materials science applications.
(S)-Bn-iQuinox serves as a chiral building block for the synthesis of quinoline-based pharmaceutical intermediates, enabling efficient access to bioactive heterocycles through Pd-catalyzed cross-coupling and C–H functionalization reactions. Its benzyl-protected indole moiety offers enhanced bench stability and facilitates straightforward purification, while the (S)-configuration ensures stereochemical fidelity in asymmetric synthesis.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: