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Structure of 23062-51-3
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Methyl 4-bromobicyclo[2.2.2]octane-1-carboxylate features a rigid, strain-promoted bicyclic framework that positions the bromine and ester groups in close spatial proximity. This configuration enables selective functionalization in synthetic sequences requiring controlled stereochemistry. The molecule exhibits excellent bench stability and compatibility with palladium-catalyzed cross-coupling reactions under standard conditions.
Methyl 4-bromobicyclo[2.2.2]octane-1-carboxylate serves as a versatile, bench-stable building block for the synthesis of strained bicyclic architectures. The bromide at the bridgehead position enables palladium-catalyzed cross-coupling reactions, while the ester group supports selective reduction, hydrolysis, or derivatization. Its rigid, three-dimensional framework provides excellent stereochemical control in asymmetric synthesis and is well-suited for constructing complex heterocycles and medicinal chemistry scaffolds.
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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-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: