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Structure of 22929-52-8
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Dihydrofuran-3(2H)-one features a reactive α,β-unsaturated carbonyl system that enables efficient Michael additions and cycloadditions. This bench-stable heterocycle integrates readily into synthetic sequences requiring electrophilic or enolizable functionality, offering high reactivity with nucleophiles under mild conditions.
Dihydrofuran-3(2H)-one serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted furan derivatives and heterocyclic scaffolds. Its inherent electrophilic character at the carbonyl carbon facilitates nucleophilic addition and cycloaddition reactions, while its stability under standard bench conditions supports straightforward handling and purification. Widely employed in medicinal chemistry and natural product synthesis, it functions as a key intermediate for constructing bioactive frameworks with predictable reactivity profiles.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 1993
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H335-H226-H302-H315-H319
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P260-P264-P270-P271-P280-P301+P310-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P370+P378-P403+P235-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: