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Structure of 10351-75-4
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1H-Benzo[d]imidazole-5,6-dicarboxylic acid features a rigid fused heterocyclic core with two carboxylic acid groups positioned for orthogonal functionalization. This configuration enables direct integration into bioactive scaffolds and materials requiring defined polarity and hydrogen-bonding capacity. The compound exhibits enhanced solubility in polar solvents and stability under standard bench conditions.
1H-Benzo[d]imidazole-5,6-dicarboxylic acid serves as a versatile heterocyclic building block for the synthesis of biologically active compounds and functional materials. Its dual carboxylic acid functionalities enable facile derivatization via amide coupling, esterification, or cyclization, while the electron-deficient imidazole core exhibits favorable stability under standard reaction conditions. The molecule functions effectively in peptide mimicry, medicinal chemistry scaffolds, and coordination chemistry due to its planar structure and defined polarity profile.
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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: