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Structure of 4760-35-4
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This chloromethyl-substituted benzimidazole delivers a reactive handle for nucleophilic functionalization. The methyl group enhances stability while the chloromethyl moiety enables efficient coupling under mild conditions. Bench-stable and moisture-tolerant, it integrates readily into synthetic sequences requiring site-specific derivatization.
2-(Chloromethyl)-1-methyl-1H-benzo[d]imidazole serves as a versatile synthetic building block for constructing biologically relevant heterocyclic scaffolds. The chloromethyl group enables efficient nucleophilic substitution reactions, facilitating the installation of diverse side chains under mild conditions. Its stability under standard laboratory handling and compatibility with common functional groups make it well-suited for medicinal chemistry campaigns and process-scale synthesis.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: