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Structure of 120122-47-6
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This trichloro ketone features a methyl-substituted nitropyrrrole moiety, combining electron-deficient character with enhanced stability. The para-nitro group enhances reactivity in electrophilic transformations, while the trichloromethyl unit provides strong inductive withdrawal. Ideal for constructing complex heterocyclic architectures under standard bench conditions.
2,2,2-Trichloro-1-(1-methyl-4-nitro-1H-pyrrol-2-yl)ethanone serves as a versatile acylating agent in heterocyclic synthesis, enabling efficient introduction of trichloromethyl ketone functionality. Its stability under standard bench conditions and compatibility with diverse functional groups facilitate straightforward incorporation into complex molecular architectures. The molecule functions effectively in electrophilic substitution and cyclization reactions, providing access to nitrogen-containing scaffolds relevant to medicinal chemistry research.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: