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Structure of 1124194-63-3
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N-(4-Formylpyridin-3-yl)acetamide features a pyridine ring bearing both a formyl group at the 4-position and an acetamide substituent at the 3-position, creating a bifunctional scaffold ideal for conjugation chemistry. The electron-deficient pyridine core enhances reactivity in nucleophilic addition processes, while the formyl group enables efficient imine formation under mild conditions. This compound serves as a key building block in the synthesis of bioconjugates and functionalized heterocycles.
N-(4-Formylpyridin-3-yl)acetamide serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-containing heterocycles via condensation and cyclization reactions. The orthogonally functionalized scaffold—combining a formyl group for nucleophilic addition and an amide-linked pyridine for metal coordination or hydrogen bonding—facilitates downstream derivatization in API synthesis. Bench-stable and readily purified by recrystallization, it functions reliably in standard reaction conditions across diverse synthetic workflows.
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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
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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: