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Structure of 1707-95-5
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This trione scaffold features a rigid, planar biindenylidene core with strategically positioned carbonyl groups, enabling robust conjugation and enhanced electron-withdrawing character. Its bench-stable nature and defined spatial orientation support precise molecular integration in advanced organic frameworks, particularly within donor-acceptor architectures for materials applications.
[1,2'-Biindenylidene]-1',3,3'(2H)-trione serves as a versatile building block in the synthesis of polycyclic aromatic systems and heterocyclic scaffolds. Its extended π-conjugated framework enables efficient Diels-Alder cycloadditions and facilitates metal-catalyzed coupling reactions. The molecule exhibits good bench stability and moderate solubility in common organic solvents, supporting straightforward purification via column chromatography. This compound functions as a key intermediate in constructing complex molecular architectures relevant to materials science and medicinal chemistry applications.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: