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Structure of 3418-21-1
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This bromomethyl-substituted dioxolane delivers a reactive handle for nucleophilic displacement, enabling efficient functionalization in synthetic workflows. The phenyl group enhances stability and modulates reactivity, while the 1,3-dioxolane ring provides excellent solubility and compatibility with diverse reaction conditions.
2-(Bromomethyl)-2-phenyl-1,3-dioxolane serves as a versatile synthon for C–C bond formation, enabling efficient access to substituted benzyl derivatives under mild conditions. Its benzylic bromide functionality exhibits high reactivity in nucleophilic substitution reactions, while the 1,3-dioxolane ring provides excellent bench stability and facilitates purification. Functions reliably in standard synthetic workflows, particularly in the construction of chiral building blocks and heterocyclic 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 : H317-H319
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Precautionary Statements : P261-P264-P272-P280-P302+P352-P362+P364-P501
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Lot numbers can be found on the outside label of a product: