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Structure of 158984-83-9
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tert-Butyl 6-hydroxy-3,4-dihydroisoquinoline-2(1H)-carboxylate features a hydroxylated dihydroisoquinoline core with a bench-stable tert-butyl ester protecting group. This moiety integrates readily into complex alkaloid scaffolds and serves as a key intermediate in the synthesis of bioactive isoquinoline derivatives. The hydroxy functionality enables direct functionalization or derivatization under mild conditions.
tert-Butyl 6-hydroxy-3,4-dihydroisoquinoline-2(1H)-carboxylate serves as a versatile intermediate in the synthesis of isoquinoline-based scaffolds, enabling efficient functionalization at the C6 position. The protected hydroxyl group offers stability and compatibility with standard coupling reactions, while the dihydroisoquinoline core facilitates downstream transformations such as oxidation to quinolines or derivatization via electrophilic substitution. Its bench-stable nature and ease of purification support scalable synthesis workflows in medicinal chemistry and process development.
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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: