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Structure of 5317-07-7
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1-Benzyl-1H-imidazole-5-carboxylic acid features a rigid imidazole core functionalized with a benzyl group at the N1 position and a carboxylic acid at the C5 position. This configuration enables direct incorporation into peptide conjugates or bioactive scaffolds, where the acidic moiety serves as a handle for amide bond formation. The compound exhibits enhanced solubility and stability under standard bench conditions, facilitating its use in medicinal chemistry campaigns targeting histamine receptor modulators and kinase inhibitors.
1-Benzyl-1H-imidazole-5-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling efficient access to imidazole-based scaffolds through standard coupling and functionalization reactions. Its carboxylic acid group facilitates amide bond formation, while the benzylated imidazole core offers enhanced stability and orthogonal reactivity. The compound exhibits excellent bench stability, ease of purification, and compatibility with common synthetic workflows for API development.
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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: