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Structure of 3592-25-4
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1,5-Dichloropentan-3-one features a symmetric diketone backbone with chlorine substituents at terminal positions, enabling direct functionalization at the C1 and C5 carbons. The molecule’s electron-deficient α-carbons facilitate nucleophilic attack, while the central ketone group supports enolization under basic conditions. This structure delivers high reactivity in synthesis of cyclic compounds and heterocyclic scaffolds.
1,5-Dichloropentan-3-one serves as a versatile bifunctional building block in synthetic organic chemistry, enabling efficient construction of heterocyclic scaffolds and functionalized intermediates. Its α,γ-dicarbonyl framework with strategically positioned chloro substituents facilitates nucleophilic substitution, cyclization, and metal-catalyzed coupling reactions. The molecule exhibits good bench stability and compatibility with common protecting group strategies, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS05,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 : H302-H315-H318-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P310-P312-P330-P332+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: