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Structure of 164148-92-9
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tert-Butyl 6-amino-3,4-dihydroisoquinoline-2(1H)-carboxylate delivers a bench-stable, electron-rich scaffold for constructing bioactive isoquinoline derivatives. The protected amine and carboxylate handle enable straightforward functionalization, while the dihydroisoquinoline core provides structural rigidity and favorable pharmacophore alignment in medicinal chemistry applications.
tert-Butyl 6-amino-3,4-dihydroisoquinoline-2(1H)-carboxylate serves as a versatile scaffold for the synthesis of isoquinoline-based bioactive molecules. The protected amine and carboxylate groups enable sequential functionalization, while the dihydroisoquinoline core supports transition-metal-catalyzed couplings and reductive amination protocols. Bench-stable and readily purified by chromatography, it facilitates efficient access to medicinally relevant heterocycles in multi-step synthetic campaigns.
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GHS Pictogram :
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GHS No : GHS06,GHS09
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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-H410
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Precautionary Statements : P264-P270-P273-P301+P310-P330-P391-P405-P501
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Lot numbers can be found on the outside label of a product: