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Structure of 5094-12-2
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This tetrahydroindole scaffold delivers a rigid, electron-rich core ideal for medicinal chemistry campaigns. The methyl substitution enhances metabolic stability and modulates lipophilicity, while the saturated pyridine ring improves solubility and processability under standard conditions.
2-Methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole serves as a versatile heterocyclic building block for medicinal chemistry applications, offering a rigid, polycyclic scaffold with defined stereochemistry. Its functional group tolerance enables direct derivatization at the C2 position and facilitates downstream coupling reactions. The compound exhibits bench stability and is compatible with standard purification protocols, making it suitable for high-throughput synthesis and structure-activity relationship studies.
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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: