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Structure of 1017279-02-5
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This bromomethyl-substituted imidazole delivers a reactive handle for nucleophilic functionalization, combining a methylated core with a para-nitro group that enhances electrophilicity. The bromomethyl moiety enables efficient coupling reactions under mild conditions, offering reliable access to complex heterocyclic architectures in synthetic and medicinal chemistry workflows.
5-(Bromomethyl)-1-methyl-4-nitro-1H-imidazole serves as a versatile bifunctional building block for the synthesis of imidazole-based scaffolds. The bromomethyl group enables efficient nucleophilic substitution reactions, while the nitro and methyl substituents provide electronic modulation and enhanced stability. This compound facilitates the construction of pharmaceutically relevant heterocycles and supports downstream functionalization 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: