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Structure of 3314-30-5
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1H-Benzo[d]imidazole-2-carbaldehyde features a rigid heteroaromatic core with a reactive aldehyde group at the 2-position, enabling direct incorporation into diverse molecular architectures. This bench-stable compound serves as a key scaffold for synthesizing bioactive imidazoles, ligands, and functional materials through efficient condensation or coupling reactions under standard conditions.
1H-Benzo[d]imidazole-2-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to biologically relevant scaffolds. Its aldehyde functionality facilitates nucleophilic addition, reductive amination, and Ugi-type coupling reactions with high reliability. The molecule exhibits excellent bench stability and compatibility with common functional groups, supporting straightforward purification and integration into multi-step synthetic sequences.
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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: