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Structure of 2922283-70-1
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This spirocyclic alcohol features a propargyl-substituted diazaspirohexene core, integrating a reactive alkyne handle with a stable, rigid framework. The pendant hydroxyl group enables further derivatization, while the constrained geometry supports selective transformations in synthetic and medicinal chemistry applications.
(5-(Prop-2-yn-1-yl)-1,2-diazaspiro[2.3]hex-1-en-5-yl)methanol serves as a versatile spirocyclic building block featuring a reactive alkyne handle and an enolizable imine functionality. It facilitates efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC) for triazole incorporation and demonstrates stability under standard bench conditions. The molecule enables straightforward derivatization in late-stage functionalization workflows and supports modular synthesis of nitrogen-containing heterocycles relevant to medicinal chemistry screening campaigns.
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GHS No : GHS02,GHS05
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Signal Word : Danger
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UN#: 2925
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Class : 4.1 (8)
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Packing Group : Ⅱ
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Hazard Statements : H226-H314
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P370+P378-P403+P235-P405-P501
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Lot numbers can be found on the outside label of a product: