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*For research and further manufacturing use only, not for direct human use.
Structure of 13044-37-6
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This brominated diene features conjugated (6Z,9Z)-configured double bonds and a terminal bromide, enabling selective functionalization in cross-coupling reactions. The stereochemically defined alkene system supports controlled synthesis of complex lipids and bioactive molecules under standard conditions.
(6Z,9Z)-18-Bromooctadeca-6,9-diene serves as a versatile bifunctional building block for the synthesis of complex unsaturated systems. The terminal bromide enables palladium-catalyzed cross-coupling reactions, while the conjugated diene moiety supports Diels-Alder cycloadditions and functional group interconversions. Its defined (Z,Z)-configuration ensures predictable stereochemical outcomes in downstream transformations, and the molecule exhibits good bench stability and ease of purification—ideal for iterative synthesis workflows in natural product and medicinal chemistry applications.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: