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Structure of 944906-95-0
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tert-Butyl 4-amino-3,4-dihydroquinoline-1(2H)-carboxylate features a bench-stable dihydroquinoline core with a strategically positioned amino group and a tert-butoxycarbonyl protecting group. This combination enables direct incorporation into synthetic sequences requiring nitrogen-directed functionalization or transition-metal-catalyzed coupling reactions. The protected amine facilitates downstream deprotection and derivatization under mild conditions.
tert-Butyl 4-amino-3,4-dihydroquinoline-1(2H)-carboxylate serves as a versatile building block for medicinal chemistry, enabling efficient access to quinoline-based scaffolds through standard functional group manipulations. The protected amine and carboxylate functionalities offer orthogonal reactivity, supporting diverse coupling and derivatization strategies. Its bench-stable nature and compatibility with common reaction conditions facilitate straightforward purification and integration into multi-step syntheses.
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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: