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Structure of 14625-39-9
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This chloromethyl-substituted benzoimidazole features a para-nitro group enhancing electrophilic reactivity, enabling efficient coupling in C–N bond formation. The pendant chloromethyl handle facilitates conjugation with nucleophiles under mild conditions, offering a robust scaffold for bioconjugation and medicinal chemistry applications.
2-(Chloromethyl)-6-nitro-1H-benzo[d]imidazole serves as a versatile bifunctional building block, enabling efficient incorporation of both nitro and chloromethyl groups into complex molecular architectures. The chloromethyl moiety facilitates nucleophilic substitution reactions under mild conditions, while the ortho-nitro group enhances electrophilicity for subsequent coupling or cyclization processes. This compound exhibits excellent bench stability and compatibility with standard purification methods, making it well-suited for use in medicinal chemistry campaigns and the synthesis of heterocyclic scaffolds.
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GHS Pictogram :
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GHS No : GHS06,GHS08
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331-H341
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: