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Structure of 58442-17-4
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1H-Benzo[d]imidazole-6-carbaldehyde features a rigid heteroaromatic core paired with a reactive aldehyde group, enabling direct incorporation into conjugate systems. This bench-stable scaffold supports efficient derivatization in synthetic and medicinal chemistry workflows.
1H-Benzo[d]imidazole-6-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to biologically relevant scaffolds. The aldehyde functionality facilitates nucleophilic additions, reductive aminations, and Ullmann-type couplings, while the imidazole core offers robust stability and orthogonal reactivity. Its bench-stable nature and compatibility with standard purification methods make it well-suited for medicinal chemistry campaigns and process development 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-H312-H315-H319-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: