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Structure of 6208-60-2
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This tetrahydroindole scaffold delivers a rigid, electron-rich core ideal for medicinal chemistry applications. Its fused bicyclic structure enhances metabolic stability and facilitates π–π interactions in target binding. The saturated pyridine ring improves solubility and reduces off-target reactivity. This framework integrates seamlessly into kinase inhibitors and CNS-targeted compounds.
2,3,4,5-Tetrahydro-1H-pyrido[4,3-b]indole serves as a versatile heterocyclic building block in medicinal chemistry, offering a rigid, planar scaffold with defined nitrogen positioning. It functions as a core motif in the synthesis of bioactive compounds and enables straightforward derivatization at multiple sites. The compound exhibits good bench stability and compatibility with standard synthetic transformations, facilitating efficient access to complex molecular architectures in drug discovery programs.
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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 : H319
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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: