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Structure of 28148-04-1
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1,3-Dibromo-2-methylpropane features a linear carbon backbone with bromine atoms at terminal positions and a methyl group on the central carbon. This structure enables efficient coupling reactions in synthetic workflows, offering high reactivity under standard conditions. The molecule's steric profile enhances selectivity in nucleophilic substitution processes, facilitating clean functionalization of heteroatoms.
1,3-Dibromo-2-methylpropane serves as a versatile bifunctional alkylating agent, enabling efficient synthesis of cyclic ethers and heterocyclic scaffolds. Its stability under ambient conditions and compatibility with diverse functional groups facilitate straightforward incorporation into complex molecular architectures. The molecule functions effectively in nucleophilic substitution reactions, particularly for constructing five- and six-membered rings via intramolecular cyclization, offering reliable access to key intermediates in synthetic organic chemistry workflows.
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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: