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Structure of 837-52-5
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7-Chloro-4-(piperazin-1-yl)quinoline features a quinoline core functionalized with a chloro group at the 7-position and a piperazinyl moiety at the 4-position, delivering enhanced solubility and tunable basicity. This scaffold integrates readily into medicinal chemistry campaigns targeting kinase inhibition and CNS-penetrant therapeutics.
7-Chloro-4-(piperazin-1-yl)quinoline serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through standard coupling and functionalization reactions. Its chloro substituent at the 7-position facilitates nucleophilic substitution, while the piperazinyl group provides a basic nitrogen for salt formation and hydrogen bonding. The molecule exhibits good bench stability and compatibility with common reaction conditions, facilitating purification and integration into complex scaffolds relevant to kinase inhibitors and CNS-targeted 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-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: