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Structure of 933992-49-5
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(R)-iPr-Quinox delivers a chiral, bench-stable quinoxaline scaffold with enhanced solubility and compatibility in asymmetric synthesis. This sterically defined heteroaromatic moiety integrates seamlessly into complex molecular architectures, enabling efficient access to bioactive scaffolds under standard conditions.
(R)-iPr-Quinox serves as a chiral auxiliary in asymmetric synthesis, enabling stereoselective construction of quinoline and quinoxaline scaffolds. Its isopropyl-substituted backbone enhances bench stability and facilitates straightforward purification. The configurationally stable chiral center promotes high diastereoselectivity in electrophilic substitution and cycloaddition reactions, making it a reliable choice for medicinal chemistry campaigns requiring controlled stereochemistry.
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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 : H315-H319
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: