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Structure of 3273-68-5
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This benzimidazole-based carboxylic acid integrates a hydrophobic aliphatic chain with a polar heterocyclic core, enabling selective interactions in bioconjugation and medicinal chemistry applications. The electron-deficient benzimidazole moiety enhances binding affinity in target-directed synthesis, while the terminal carboxyl group facilitates derivatization under standard coupling conditions.
4-(2-Oxo-3H-benzimidazol-1-yl)butanoic acid serves as a versatile building block for the synthesis of bioactive heterocycles, enabling efficient construction of benzimidazole-containing scaffolds. Its carboxylic acid functionality facilitates conjugation via amide bond formation, while the aromatic imidazole core exhibits good bench stability and compatibility with standard functional group transformations. The molecule functions effectively in peptide coupling and macrocyclization strategies, offering practical 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 : 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: