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Structure of 142335-42-0
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This chiral tetrahydroisoquinoline derivative features a protected amine, a hydroxyl group, and a carboxylic acid—ideal for constructing complex alkaloid scaffolds. The tert-butoxycarbonyl group enables selective deprotection during peptide coupling or cyclization sequences. Designed for synthetic efficiency in medicinal chemistry applications.
(S)-2-(tert-Butoxycarbonyl)-7-hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid serves as a versatile chiral building block for the synthesis of substituted tetrahydroisoquinoline scaffolds. The protected amine and carboxylic acid functionalities enable orthogonal derivatization, while the phenolic hydroxyl group supports selective functionalization. Bench-stable and compatible with standard coupling and reduction protocols, it facilitates efficient access to bioactive analogs 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-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: