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Structure of 40332-16-9
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2-(1H-Benzo[d]imidazol-1-yl)acetic acid features a benzimidazole core linked via a methylene bridge to a carboxylic acid group, enabling integration into bioactive molecules. The aromatic imidazole moiety imparts strong hydrogen-bonding capacity and enhanced metabolic stability. This scaffold supports efficient conjugation in medicinal chemistry campaigns targeting receptor modulation.
2-(1H-Benzo[d]imidazol-1-yl)acetic acid serves as a versatile building block for bioactive heterocycles, enabling efficient incorporation of the benzimidazole pharmacophore into drug-like scaffolds. Its carboxylic acid functionality facilitates conjugation via amide or ester linkages, while the benzoimidazole moiety provides structural rigidity and hydrogen-bonding capacity. The compound exhibits good bench stability and compatibility with standard peptide coupling protocols, supporting its use in medicinal chemistry campaigns targeting kinase inhibitors and CNS-active agents.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: