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Structure of 36273-11-7
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This chloromethyl-substituted diazabicyclooctane salt features a reactive electrophilic handle ideal for nucleophilic displacement reactions. The quaternary nitrogen center imparts high solubility in polar solvents and enhances reactivity in synthetic transformations. Designed for efficient functionalization in medicinal chemistry and polymer conjugation workflows.
1-(Chloromethyl)-1,4-diazabicyclo[2.2.2]octan-1-ium chloride serves as a versatile alkylating agent in synthetic organic chemistry, enabling efficient functionalization of nucleophiles under mild conditions. Its quaternary ammonium structure provides excellent stability and solubility in polar solvents, facilitating clean reactions with amines, thiols, and enolates. The chloride counterion enhances reactivity while maintaining bench stability, making it ideal for constructing nitrogen-containing heterocycles and bioactive scaffolds in medicinal 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: