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Structure of 868-72-4
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Dimethyl 2,5-dibromohexanedioate features two bromine substituents flanking a six-carbon chain, enabling selective functionalization in organic synthesis. This dibromo diester serves as a key intermediate for constructing complex cyclic and acyclic frameworks under mild conditions. The molecule's stability and defined stereochemical handle facilitate controlled transformations in multistep sequences.
Dimethyl 2,5-dibromohexanedioate serves as a versatile dihalogenated building block for the synthesis of substituted cyclohexanes and functionalized heterocycles. Its brominated aliphatic framework enables efficient stereoselective transformations via nucleophilic substitution or elimination pathways. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for use in modular synthetic sequences targeting complex scaffolds in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-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: