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Structure of 5649-36-5
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2,6-Dimethyl-1H-indole features a sterically hindered indole core with methyl groups at the 2 and 6 positions, enhancing stability and modulating electronic properties. This substitution pattern reduces reactivity at the aromatic ring while preserving the nitrogen lone pair for coordination or functionalization. The molecule exhibits favorable solubility in organic solvents and serves as a robust scaffold in synthetic applications requiring controlled reactivity and defined steric profiles.
2,6-Dimethyl-1H-indole serves as a valuable building block in medicinal chemistry and heterocyclic synthesis, offering enhanced stability and defined regiochemistry due to methyl substitution at the 2- and 6-positions. Its electron-rich indole core facilitates electrophilic aromatic substitution and acts as a scaffold for C–H functionalization, enabling efficient access to complex alkaloid-like structures. The compound exhibits good bench stability, ease of handling, and compatibility with standard purification methods, making it well-suited for iterative synthetic campaigns in API development and target-oriented synthesis.
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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: