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Structure of 50741-36-1
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1,2,3,4-Tetrahydroquinoline-6-carbonitrile features a fused heterocyclic core with a nitrile group at the C6 position, enabling direct functionalization in synthetic routes. This electron-deficient scaffold integrates readily into pharmaceutical intermediates and bioactive molecule frameworks. The saturated ring system enhances metabolic stability while maintaining reactivity for further derivatization under standard conditions.
1,2,3,4-Tetrahydroquinoline-6-carbonitrile serves as a versatile scaffold for medicinal chemistry and synthetic organic applications. The nitrile group enables downstream functionalization via hydrolysis or nucleophilic addition, while the saturated quinoline core offers enhanced metabolic stability and favorable pharmacokinetic properties. It functions as a key building block in the synthesis of heterocyclic APIs and exhibits good bench stability and ease of purification in standard reaction workflows.
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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: