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Structure of 123910-26-9
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(R)-2-(tert-Butoxycarbonyl)-2,3,4,9-tetrahydro-1h-pyrido[3,4-b]indole-3-carboxylic acid features a stereochemically defined chiral center and a protected carboxylic acid group, enabling its use in asymmetric synthesis. The tert-butoxycarbonyl moiety provides stability and facilitates selective deprotection during peptide or heterocyclic scaffold elaboration. This intermediate integrates readily into complex molecular architectures requiring controlled functionalization under standard bench conditions.
(R)-2-(tert-Butoxycarbonyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylic acid serves as a key chiral building block for the synthesis of pyridoindole-based pharmaceutical scaffolds. The tert-butyl carbamate group provides excellent stability and orthogonal deprotection compatibility, enabling efficient functionalization at the nitrogen. The carboxylic acid functionality facilitates coupling reactions and derivatization under standard peptide and medicinal chemistry conditions. This compound exhibits high bench stability and is well-suited for multi-step syntheses requiring precise stereocontrol and functional group tolerance.
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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: