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Structure of 70343-13-4
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7-Methyl-5-nitro-1H-indole-2,3-dione features a fused tricyclic core with electron-deficient character, enabling efficient participation in cycloaddition and condensation reactions. The para-nitro group enhances reactivity while the methyl substitution improves solubility and stability under standard conditions. This compound serves as a versatile scaffold for bioactive molecule synthesis.
7-Methyl-5-nitro-1H-indole-2,3-dione serves as a versatile building block in heterocyclic synthesis, enabling efficient access to polycyclic scaffolds via cycloaddition and condensation reactions. Its electron-deficient quinone core facilitates nucleophilic addition and Diels-Alder transformations, while the methyl and nitro groups offer orthogonal handles for further functionalization. Bench-stable and readily purified by recrystallization, it functions effectively in both small-molecule medicinal chemistry and materials science 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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: