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Structure of 22094-18-4
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1,3-Dibromo-2,2-dimethoxypropane delivers a robust difunctional bromination capability in organic synthesis. The geminal dimethoxy groups stabilize the adjacent carbon center, enhancing reactivity while maintaining bench stability. This reagent enables efficient α-bromination of carbonyl compounds and facilitates tandem substitution reactions under mild conditions.
1,3-Dibromo-2,2-dimethoxypropane serves as a reliable dibrominating agent for enolizable carbonyl compounds and activated methylene groups, enabling efficient α,α′-dibromination under mild conditions. Its dimethoxy protection stabilizes the molecule against hydrolysis, enhancing bench stability and simplifying handling. The reagent exhibits high functional group tolerance and facilitates clean reaction profiles with minimal side products, making it particularly valuable in the synthesis of brominated intermediates for pharmaceutical and agrochemical applications.
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Lot numbers can be found on the outside label of a product: