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Structure of 138891-51-7
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Imidazo[1,5-a]pyridine-1-carboxylic acid features a rigid, planar heterocyclic core with a carboxylic acid group enabling direct conjugation or derivatization. This scaffold exhibits enhanced metabolic stability and favorable solubility characteristics, making it suitable for medicinal chemistry applications requiring bioactive molecular frameworks with defined polarity and hydrogen-bonding capacity.
Imidazo[1,5-a]pyridine-1-carboxylic acid serves as a versatile scaffold for medicinal chemistry and synthetic organic applications, enabling efficient construction of biologically relevant heterocycles. The carboxylic acid functionality facilitates direct derivatization via amide coupling, esterification, or decarboxylation, while the fused imidazopyridine core exhibits robust bench stability and compatibility with standard reaction conditions. Its defined regiochemistry supports predictable functionalization, making it a practical building block for drug discovery campaigns requiring nitrogen-rich, planar aromatic systems.
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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: