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Structure of 36236-76-7
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This bromomethyl-substituted dioxolane offers a stable, moisture-tolerant handle for C–C bond formation via nucleophilic displacement. The geminal dimethyl groups enhance steric protection, while the 1,3-dioxolane ring provides conformational rigidity and improved solubility in polar organic solvents.
4-(Bromomethyl)-2,2-dimethyl-1,3-dioxolane serves as a stable, bench-friendly synthon for introducing bromomethyl groups under mild conditions. Its cyclic acetal structure confers enhanced stability and compatibility with diverse functional groups, enabling efficient nucleophilic substitution reactions. The reagent facilitates the construction of complex heterocyclic systems and acts as a versatile building block in the synthesis of pharmaceutical intermediates and agrochemical scaffolds.
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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#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H227-H315-H317-H318-H335
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Precautionary Statements : P210-P261-P264-P271-P272-P280-P302+P352-P304+P340-P362-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: