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Structure of 39603-24-2
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5,7-Dimethyl-1H-indole-2,3-dione features a sterically hindered, electron-deficient quinone core that enhances stability and reactivity in cycloaddition processes. This scaffold integrates readily into synthetic routes for bioactive heterocycles and serves as a robust building block in medicinal chemistry campaigns requiring modular access to fused ring systems under standard conditions.
5,7-Dimethyl-1H-indole-2,3-dione serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted indole scaffolds via cycloaddition and condensation reactions. Its enhanced stability and defined regiochemistry facilitate straightforward functionalization, making it valuable for medicinal chemistry campaigns and heterocycle synthesis. The molecule's dual carbonyl groups and electron-rich core support diverse transformations under mild conditions, offering reliable performance in bench-scale applications.
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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: