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Structure of 66521-54-8
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This enone features a conjugated system linking a dimethylamino donor group to a 2-pyridinyl acceptor, creating a strong push–pull architecture. The molecule exhibits enhanced solubility in organic solvents and stability under standard bench conditions, enabling straightforward integration into synthetic pathways for heterocyclic derivatives and photoactive materials.
3-(Dimethylamino)-1-(2-pyridinyl)-2-propen-1-one serves as a versatile enone building block in synthetic organic chemistry, enabling efficient construction of nitrogen-containing heterocycles. Its conjugated system supports Michael additions and cyclization reactions under mild conditions, with the dimethylamino group enhancing nucleophilicity and the pyridine moiety providing orthogonal reactivity. Bench-stable and readily purified by chromatography, it facilitates scalable synthesis of pharmacologically relevant scaffolds.
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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: