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Structure of 3212-75-7
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2-Cycloocten-1-ol features a conjugated enol system with enhanced stability due to resonance delocalization. This bench-stable alcohol bears a terminal alkene and hydroxyl group, enabling direct functionalization in synthetic sequences. The rigid cyclooctenyl framework supports stereoselective transformations, making it valuable for building complex cyclic architectures in organic synthesis.
2-Cycloocten-1-ol serves as a versatile intermediate in synthetic organic chemistry, offering a reactive allylic alcohol functionality within a strained cyclic framework. Its structure enables straightforward derivatization via oxidation, protection, or metal-catalyzed coupling reactions. The compound exhibits sufficient bench stability for routine handling and facilitates efficient access to functionalized cyclooctane derivatives and heterocyclic scaffolds through established transformation pathways.
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GHS Pictogram :
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GHS No : GHS02
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Signal Word : Danger
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UN#: 1987
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H225-H302-H312-H332
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P370+P378-P501
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Lot numbers can be found on the outside label of a product: