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Structure of 61010-04-6
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2-Chloro-3-(hydroxymethylene)cyclohex-1-enecarbaldehyde features a reactive α,β-unsaturated aldehyde paired with a pendant hydroxymethylene group, enabling direct conjugate addition and subsequent cyclization. This bifunctional scaffold facilitates rapid access to complex carbocyclic architectures under mild conditions.
2-Chloro-3-(hydroxymethylene)cyclohex-1-enecarbaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized cyclohexene scaffolds. Its conjugated enal system and pendant hydroxymethylene group facilitate Diels-Alder reactions, nucleophilic additions, and subsequent cyclizations under mild conditions. The molecule exhibits good bench stability and tolerates common functional groups, making it well-suited for iterative synthesis workflows in medicinal chemistry and natural product derivatization.
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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-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: