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Structure of 33170-72-8
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2-Bromo-1,1-dimethoxypropane serves as a selective alkylating agent featuring a reactive bromide and two methoxy groups that stabilize the adjacent carbon. This configuration enables efficient coupling in nucleophilic substitution reactions under mild conditions. The molecule’s bench-stable nature supports reliable handling in synthetic workflows involving carbonyl derivatives or heteroatom nucleophiles.
2-Bromo-1,1-dimethoxypropane serves as a reliable alkylating agent for the selective introduction of propyl groups under mild conditions. Its dimethoxy protection stabilizes the carbonyl equivalent, enhancing bench stability and minimizing side reactions. The molecule facilitates efficient nucleophilic substitution with amines, thiols, and enolates, enabling straightforward access to functionalized intermediates in medicinal chemistry and process synthesis.
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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: