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*For research and further manufacturing use only, not for direct human use.
Structure of 170097-67-3
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This tetrahydroisoquinoline derivative features a tert-butoxycarbonyl-protected amine and a carboxylic acid group at the 6-position, enabling direct incorporation into peptide conjugates or heterocyclic scaffolds. The Boc group ensures stability during synthesis, while the electron-rich aromatic core facilitates transition metal-catalyzed coupling reactions under standard conditions.
2-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-6-carboxylic acid serves as a versatile building block for the synthesis of tetrahydroisoquinoline-based scaffolds. The tert-butoxycarbonyl group provides robust protection of the amine, enabling stable handling and compatibility with diverse coupling reactions. The carboxylic acid functionality facilitates efficient derivatization and conjugation, supporting applications in medicinal chemistry and peptide synthesis. Its structural integrity and functional group orthogonality make it a reliable intermediate in multi-step synthetic sequences.
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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: