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Structure of 1871-67-6
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(E)-Oct-2-enoic acid features a conjugated enoic system with defined (E)-stereochemistry, enabling precise incorporation into lipid-based scaffolds and functional materials. This bench-stable, moisture-tolerant reagent delivers high regioselectivity in coupling reactions and serves as a key building block for bioactive esters and polymer precursors under standard conditions.
(E)-Oct-2-enoic acid serves as a versatile building block for conjugated unsaturated systems, enabling efficient Michael additions and Diels-Alder reactions. Its stable (E)-configuration facilitates reproducible stereocontrol in synthetic sequences, while the carboxylic acid functionality allows direct derivatization or activation for amide bond formation. The compound exhibits good bench stability and is readily purified by recrystallization, making it well-suited for use in medicinal chemistry and materials synthesis workflows.
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GHS Pictogram :
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GHS No : GHS05
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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 : Ⅱ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: