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Structure of 144876-36-8
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1H-Benzo[d]imidazole-4-carbaldehyde features a rigid heteroaromatic core with a reactive aldehyde group at the 4-position, enabling direct incorporation into Schiff base formations. This functionality supports rapid conjugation in medicinal chemistry and materials synthesis, where precise molecular architecture is critical. The compound exhibits high thermal stability and compatibility with diverse reaction conditions.
1H-Benzo[d]imidazole-4-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to biologically relevant scaffolds. Its aldehyde functionality facilitates nucleophilic additions, reductive aminations, and Ugi-type couplings, while the imidazole core offers robust stability and moderate polarity. The compound exhibits favorable bench stability and ease of purification, making it well-suited for parallel synthesis campaigns and medicinal chemistry exploration.
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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: