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Structure of 149353-95-7
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This tetrahydroisoquinoline derivative features a protected amine and carboxylic acid group, enabling direct incorporation into peptide synthesis. The tert-butoxycarbonyl moiety ensures stability during reaction sequences, while the electron-rich aromatic core supports efficient coupling under standard conditions.
2-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-7-carboxylic acid serves as a versatile building block for the synthesis of isoquinoline-based scaffolds in medicinal chemistry. The tert-butyl ester group enables orthogonal protection and convenient deprotection under mild acidic conditions, while the carboxylic acid functionality supports direct coupling reactions. Its stability and compatibility with standard peptide and heterocyclic coupling protocols make it ideal for iterative synthesis workflows.
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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: