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Structure of 479-59-4
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This tetrahydroquinoline scaffold delivers a rigid, electron-rich heterocyclic core ideal for medicinal chemistry applications. Featuring a well-defined fusion of pyridine and quinoline systems, it enables precise spatial positioning in bioactive molecules. The saturated ring system enhances metabolic stability while maintaining favorable solubility profiles.
2,3,6,7-Tetrahydro-1H,5H-pyrido[3,2,1-ij]quinoline serves as a versatile heterocyclic scaffold in medicinal chemistry, offering a rigid, planar core with defined nitrogen positioning. It functions as a key building block for bioactive molecules, enabling efficient access to fused polycyclic systems via standard functionalization and coupling reactions. The compound exhibits good bench stability and facilitates downstream derivatization due to its well-defined reactivity profile and compatibility with common protecting group strategies.
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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: