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Structure of 1396777-92-6
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tert-Butyl 6-chloro-3,4-dihydro-2,7-naphthyridine-2(1H)-carboxylate features a sterically hindered tert-butyl ester and a chlorine-substituted naphthyridine core, enabling robust coupling reactions. This bench-stable intermediate integrates seamlessly into medicinal chemistry campaigns requiring electron-deficient heterocycles for transition metal-catalyzed transformations.
tert-Butyl 6-chloro-3,4-dihydro-2,7-naphthyridine-2(1H)-carboxylate serves as a versatile building block for the synthesis of naphthyridine-based scaffolds. The chloro group enables palladium-catalyzed cross-coupling reactions, while the protected carboxylic acid facilitates subsequent functionalization. Its bench-stable nature and compatibility with standard synthetic workflows make it ideal for medicinal chemistry and process development applications.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: