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Structure of 341010-40-0
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6-Chloro-5-quinolinamine delivers a reactive chloro substituent at the 6-position and a primary amine at the 5-position on the quinoline scaffold. This configuration enables direct coupling reactions in medicinal chemistry and materials synthesis, where regioselective functionalization is critical. The molecule exhibits favorable solubility in common organic solvents and stability under standard bench conditions.
6-Chloro-5-quinolinamine serves as a versatile building block in medicinal chemistry, enabling direct coupling reactions via its amino and chloro functionalities. The ortho-chloro group facilitates palladium-catalyzed cross-coupling, while the primary amine supports derivatization through acylation or azo coupling. Its stability under standard reaction conditions and compatibility with diverse functional groups make it a practical reagent for constructing quinoline-based scaffolds in 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-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: