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Structure of 1004-24-6
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This cyclohexylmethanol derivative features a methylidene group at the 4-position, conferring enhanced reactivity in ring-functionalization and allylation processes. The hydroxymethyl moiety enables straightforward derivatization, while the exocyclic double bond supports selective transformations under mild conditions. A bench-stable, moisture-tolerant building block for complex molecular architectures.
(4-Methylidenecyclohexyl)methanol serves as a versatile building block in synthetic organic chemistry, enabling access to functionalized cyclohexane derivatives through selective transformations. Its exocyclic methylene group facilitates conjugate additions and Diels-Alder reactions, while the primary alcohol allows for straightforward derivatization, oxidation, or protection. The compound exhibits good bench stability and compatibility with standard purification techniques, making it suitable for iterative synthesis workflows in medicinal chemistry and process development.
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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-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: