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Structure of 51716-63-3
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cis-Tetrahydropentalene-2,5(1H,3H)-dione features a rigid, fused bicyclic framework with two ketone groups in close proximity, enabling selective reactivity in cycloaddition and Diels-Alder processes. The cis configuration enhances molecular polarity and facilitates controlled transformations under mild conditions. This scaffold serves as a valuable building block for complex heterocycles and natural product analogs.
cis-Tetrahydropentalene-2,5(1H,3H)-dione serves as a valuable bicyclic synthon in synthetic organic chemistry, offering defined stereochemistry and dual carbonyl functionality for Diels-Alder reactions and heterocycle construction. Its bench-stable nature and predictable reactivity facilitate efficient access to complex polycyclic frameworks relevant to natural product synthesis and medicinal chemistry 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: