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Structure of 1187933-14-7
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(S)-1-Boc-3,4-dihydro-2H-quinoline-2-carboxylic acid features a chiral quinoline core with a bench-stable Boc-protected carboxylic acid moiety, enabling direct incorporation into peptide-like scaffolds. The dihydroquinoline ring system offers enhanced solubility and reduced oxidation susceptibility compared to aromatic analogs, facilitating use in asymmetric synthesis and medicinal chemistry applications.
(S)-1-Boc-3,4-dihydro-2H-quinoline-2-carboxylic acid serves as a versatile chiral building block for the synthesis of bioactive heterocycles and pharmaceutical intermediates. The Boc-protected amine enables orthogonal functionalization, while the dihydroquinoline core supports diverse transformations including hydrogenation, electrophilic substitution, and coupling reactions. Bench-stable and readily purified, it facilitates efficient access to complex scaffolds in medicinal chemistry campaigns.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: