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Structure of 1124-29-4
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5-Acetylpyridin-2(1H)-one features a pyridinone core with a strategically positioned acetyl group, enabling direct integration into heterocyclic scaffolds. This bench-stable derivative exhibits enhanced solubility and reactivity in polar solvents, facilitating efficient coupling reactions under mild conditions. The ketone functionality serves as a key handle for derivatization in medicinal chemistry and materials science applications.
5-Acetylpyridin-2(1H)-one serves as a versatile building block for heterocyclic synthesis, enabling efficient access to pyridone-based scaffolds through standard functional group transformations. Its acetyl group facilitates electrophilic substitution and condensation reactions, while the enolizable ketone and lactam functionalities offer orthogonal reactivity for C–C and C–N bond formation. Bench-stable and readily purified by recrystallization, it functions effectively in multi-step syntheses targeting medicinal chemistry intermediates and functional materials.
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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: