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Structure of 46006-36-4
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1H-benzo[d]imidazole-4-carboxylic acid features a rigid, electron-deficient heterocyclic core paired with a carboxylic acid handle, enabling direct conjugation in peptide and macrocyclic scaffolds. This bench-stable compound integrates readily into bioactive molecule design, offering enhanced metabolic stability and improved solubility profiles in polar solvents.
1H-benzo[d]imidazole-4-carboxylic acid serves as a versatile scaffold for the synthesis of bioactive heterocycles, enabling efficient functionalization at the carboxylic acid and imidazole nitrogen sites. Its bench-stable nature and compatibility with standard coupling reactions facilitate direct incorporation into pharmaceutical intermediates and macrocyclic systems. Functions effectively in peptide coupling, amide formation, and transition-metal-catalyzed transformations, offering robust utility in medicinal chemistry 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 : H319
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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: