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Structure of 179898-00-1
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tert-Butyl 4-oxo-3,4-dihydroquinoline-1(2H)-carboxylate features a rigid, electron-deficient quinoline core with a masked carbonyl functionality, enabling direct incorporation into synthetic sequences without pre-activation. This bench-stable derivative facilitates efficient access to complex heterocycles through controlled cyclization or coupling reactions under standard conditions.
tert-Butyl 4-oxo-3,4-dihydroquinoline-1(2H)-carboxylate serves as a versatile scaffold for the synthesis of quinoline-based heterocycles, enabling efficient access to medicinally relevant architectures. Its functionality supports diverse transformations including nucleophilic additions, reductive aminations, and transition-metal-catalyzed couplings. The tert-butyl ester group provides excellent bench stability and facilitates straightforward deprotection under mild acidic conditions, enhancing its utility in multi-step synthetic sequences.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: