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Structure of 1135283-53-2
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5-(Trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde features a rigid heteroaromatic core bearing a trifluoromethyl group and an aldehyde functionality at the 3-position. This electron-deficient scaffold enables direct coupling in cross-coupling reactions and serves as a key building block for bioactive molecules in medicinal chemistry.
5-(Trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde serves as a versatile heterocyclic building block for medicinal chemistry and materials science. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the aldehyde functionality enables diverse transformations including reductive amination, Wittig reactions, and condensation with hydrazines or hydroxylamines. Bench-stable and compatible with standard purification methods, it functions effectively in multistep syntheses of bioactive molecules and functionalized scaffolds.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H319
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: