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Structure of 1092287-45-0
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2-Aminoquinoline-7-carboxylic acid integrates a nitrogen-rich heterocyclic core with complementary amino and carboxylic acid functionalities, enabling direct conjugation in bioconjugation workflows. This scaffold delivers enhanced solubility and stability under physiological conditions, facilitating efficient incorporation into probe architectures for target engagement studies.
2-Aminoquinoline-7-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling direct incorporation into heterocyclic scaffolds via amidation, coupling, or cyclization reactions. Its dual functionality—amine and carboxylic acid—facilitates modular synthesis of bioactive molecules, particularly in kinase inhibitor and antimalarial research. The compound exhibits good bench stability and ease of purification, supporting reliable use in multi-step synthetic sequences.
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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: