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Structure of 40615-02-9
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1,2,3,4-Tetrahydroquinolin-3-amine features a saturated quinoline core with a primary amine at the 3-position, offering enhanced solubility and reactivity compared to aromatic analogs. This scaffold integrates readily into medicinal chemistry libraries, serving as a key intermediate for kinase inhibitors and CNS-targeted therapeutics. The benzylic amine functionality enables straightforward derivatization under mild conditions.
1,2,3,4-Tetrahydroquinolin-3-amine serves as a versatile scaffold in medicinal chemistry, enabling efficient access to bioactive heterocycles through standard functionalization. Its amine functionality facilitates straightforward derivatization via alkylation, acylation, or coupling reactions. The compound exhibits good bench stability and compatibility with common purification methods, making it well-suited for iterative synthesis campaigns targeting CNS-active molecules and kinase inhibitors.
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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: