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Structure of 79815-18-2
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This chiral ester features a rigid, electron-rich tetrahydropyridoindole scaffold ideal for asymmetric synthesis. The (S)-configured methyl ester group enables stereocontrolled derivatization in medicinal chemistry campaigns. Bench-stable and readily soluble in common organic solvents, it serves as a high-fidelity building block for complex heterocyclic systems.
(S)-Methyl 2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate serves as a versatile chiral building block for the synthesis of complex indole-based scaffolds. Its well-defined stereochemistry and functionalized pyridine-indole core enable reliable transformations in medicinal chemistry workflows. The ester group facilitates selective derivatization, while the tetrahydro-pyridoindole framework exhibits robust bench stability and compatibility with standard coupling and reduction protocols.
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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: