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Structure of 18719-24-9
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7-Octenoic acid features a conjugated enoate system enabling direct participation in Michael additions and Diels-Alder reactions. The terminal alkene facilitates selective functionalization, while the carboxylic acid group provides a handle for derivatization. This structure supports efficient integration into synthetic pathways requiring electron-deficient olefins or bifunctional intermediates.
7-Octenoic acid serves as a versatile unsaturated carboxylic acid building block for synthesizing bioactive lipids, fatty acid derivatives, and functionalized polymers. Its terminal alkene enables reliable Michael additions, hydrogenations, and cross-coupling reactions. The molecule exhibits good bench stability and facilitates straightforward purification via distillation or chromatography, making it suitable for use in medicinal chemistry campaigns and materials science applications.
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GHS Pictogram :
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GHS No : GHS05,GHS07,GHS09
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Signal Word : Danger
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UN#: 3265
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H314-H410
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Precautionary Statements : P260-P264-P270-P273-P280-P301+P330+P331-P304+P340-P330-P363-P391-P405-P501
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Lot numbers can be found on the outside label of a product: