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Structure of 779-90-8
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This triketone features a central benzene ring substituted with three acetyl groups at the 1,3,5-positions, delivering high symmetry and enhanced stability. The electron-deficient carbonyl moieties enable efficient participation in nucleophilic addition reactions, particularly in transition metal-catalyzed coupling processes. Bench-stable and readily soluble in common organic solvents, it serves as a robust scaffold for constructing complex molecular architectures in synthetic organic chemistry and materials science applications.
1,1',1''-(Benzene-1,3,5-triyl)tris(ethan-1-one) serves as a versatile triketone scaffold for constructing complex polycyclic architectures. Its three ketone functionalities enable sequential aldol condensations, reductive aminations, and metal-catalyzed couplings, facilitating rapid access to diverse heterocyclic systems. The molecule exhibits good bench stability and simplifies purification due to predictable chromatographic behavior, making it a practical building block in multi-step synthetic sequences.
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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: