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Structure of 53910-13-7
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S-Indacene-1,3,5,7(2H,6H)-tetrone features a rigid, planar polycyclic framework with four carbonyl groups positioned at key fusion junctions. This electron-deficient architecture enhances charge transport properties and facilitates π-stacking interactions, making it well-suited for organic semiconductor applications. The tetrone motif contributes to high oxidative stability and predictable reactivity in cross-coupling transformations.
S-Indacene-1,3,5,7(2H,6H)-tetrone serves as a versatile polycyclic building block for constructing extended π-systems and functionalized heterocycles. Its four carbonyl groups enable selective reactivity in nucleophilic addition and condensation reactions, facilitating access to complex aromatic frameworks. The molecule exhibits bench stability and compatibility with standard synthetic protocols, supporting efficient purification and integration into multi-step sequences for advanced materials and molecular 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: