10220-83-4

Basic information

• Product Name: 1,4-Cyclohexanedione,1,4-dioxime
• Synonyms: 1,4-Cyclohexanedione,dioxime (6CI,7CI,8CI,9CI); 1,4-Bis(hydroxyimino)cyclohexane;1,4-Cyclohexanedioxime; NSC 145140; p-Cyclohexanedione dioxime
• CAS NO: 10220-83-4
• Molecular Formula: C6H10 N2 O2
• Molecular Weight: 142.158
• Mol File: 10220-83-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,4-Cyclohexanedione,1,4-dioxime(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Cyclohexanedione,1,4-dioxime(10220-83-4)
• EPA Substance Registry System: 1,4-Cyclohexanedione,1,4-dioxime(10220-83-4)

Safety Data

• Hazardous Substances Data: 10220-83-4(Hazardous Substances Data)

Usage

Type of compound

Dioxime derivative of cyclohexanedione

Common use

Building block for the synthesis of various organic compounds

Chelating properties

Ability to chelate metal ions

Applications

a. Coordination chemistry
b. Metal extraction processes
c. Reagent in organic synthesis for the formation of nitrogen-containing compounds
d. Pharmaceutical and agrochemical industries
e. Environmental and analytical applications

Versatile reactivity

Can form stable complexes with metal ions

Upstream product

• 637-88-7 1,4-Cyclohexanedione 
• 556-48-9 1,4-Cyclohexanediol 
• 64-17-5 ethanol 
• 89415-89-4 1,4-dichloro-1,4-dinitro-cyclohexane 
• 18993-06-1 trans-1,4-Dinitroso-1,4-dichlorcyclohexan 

Downstream Products

• 64945-67-1 1.4-Bis-dimethylamino-cyclohexan 
• 35197-79-6 N-(4-formamidocyclohexyl)formamide 
• 18993-06-1 trans-1,4-Dinitroso-1,4-dichlorcyclohexan 
• 106150-80-5 {Cl(C₁₀H₈N₂)2OsNOHC₆H₈NOH}⁽¹⁺⁾*PF₆^(1-)={Cl(C₁₀H₈N₂)2OsNOHC₆H₈NOH}PF₆ 
• 2678-67-3 N₁,N₄-dimethylcyclohexane-1,4-diamine 
• 3114-70-3 trans-1,4-diaminocyclohexane 
• 87373-54-4 trans-1,4-dibromo-1,4-dinitrosocyclohexane 
• 87373-52-2 1,4-dibromo-2,3-diazabicyclo<2.2.2>oct-2-ene N,N'-dioxide 
• 13094-38-7 C₈H₁₄N₂O₆S₂ 
• 2077-92-1 N,N'-(trans-cyclohexane-1,4-diyl)-bis-acetamide; trans-1.4-bis-acetylamino-cyclohexane 
• 2840-91-7 cis-cyclohexane-1,4-diacetamide 
• 89415-61-2 trans-1,4-Dibrom-1,4-dinitro-cyclohexan 
• 89415-61-2 cis-1,4-dibromo-1,4-dinitro-cyclohexane 
• 58426-26-9 trans-1,4-dichloro-1,4-dinitrosocyclohexane 

Relevant articles and documents

From 1,4-diketones to N-vinyl derivatives of 3,3′-bipyrroles and 4,8-dihydropyrrolo[2,3-f]indole in just two preparative steps

Dioximes of hexane-2,5-dione and cyclohexane-1,4-dione react with acetylene in an autoclave (KOH/DMSO, 100°C, 1h, initial pressure 14atm) to give 2,2′-dimethyl-1,1′-divinyl-[3,3′]bipyrrole and 1,5-divinyl-4,8-dihydropyrrolo[2,3-f]indole in 12% and 6% yiel

Dioximate- and Bis(salicylaldiminate)-bridged titanium and zirconium alkoxides: Structure elucidation by mass spectrometry

The treatment of titanium alkoxides with 1,5-pentanedioxime or 2,5-hexanedioxime resulted in the formation of complexes [{TiL(OR) 2}2] in which the dioximate ligands (L) bridge a dimeric Ti2(μ2-OR)2 u