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Structure of 112892-88-3
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Bicyclo[4.2.0]octa-1,3,5-triene-3-carbaldehyde features a rigid polycyclic framework with conjugated diene and aldehyde functionalities, enabling participation in Diels-Alder reactions and functional group interconversions under standard conditions. The strained bridgehead carbon supports high reactivity, while the aldehyde serves as a key handle for downstream derivatization.
Bicyclo[4.2.0]octa-1,3,5-triene-3-carbaldehyde serves as a versatile dienophile and carbonyl building block in Diels-Alder reactions and functional group interconversions. Its strained bicyclic framework enhances reactivity while maintaining bench stability, enabling efficient access to complex polycyclic architectures. The aldehyde functionality facilitates downstream transformations such as reduction, oxidation, or nucleophilic addition, supporting applications in natural product synthesis and medicinal chemistry lead generation.
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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 : H227-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: