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Structure of 36122-35-7
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3-Phenylfuran-2,5-dione features a fused furanone core bearing a phenyl substituent at the 3-position, conferring enhanced π-conjugation and planarity. This electron-deficient dienone scaffold serves as a key building block in heterocyclic synthesis, particularly for constructing complex polycyclic frameworks via Diels–Alder reactions and transition-metal-catalyzed couplings.
3-Phenylfuran-2,5-dione serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted furan derivatives through standard functional group transformations. Its electron-deficient diketone framework facilitates nucleophilic addition and cycloaddition reactions, while its bench-stable crystalline form simplifies handling and purification. This compound functions as a key intermediate in the construction of bioactive scaffolds and fused polycyclic systems relevant to medicinal chemistry and materials science.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P341-P312-P330-P363-P501
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Lot numbers can be found on the outside label of a product: