4322-62-7

Basic information

• Product Name: 1,2,3-Cyclohexanetrione
• Synonyms: 1,2,3-Cyclohexanetrione
• CAS NO: 4322-62-7
• Molecular Formula: C₆H₆O₃
• Molecular Weight: 126.11
• Mol File: 4322-62-7.mol
• Article Data: 6

Chemical Properties

• Melting Point: 103-104 °C
• Boiling Point: 238.3±23.0 °C(Predicted)
• Appearance: /
• Density: 1.314±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,2,3-Cyclohexanetrione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3-Cyclohexanetrione(4322-62-7)
• EPA Substance Registry System: 1,2,3-Cyclohexanetrione(4322-62-7)

Safety Data

• Hazardous Substances Data: 4322-62-7(Hazardous Substances Data)

Usage

Structure

Cyclic triketone with three carbonyl groups attached to a cyclohexane ring

Physical State

Stable solid at room temperature

Solubility

Slightly soluble in water

Applications

a. Organic synthesis
b. Chemical research as a building block for various chemical reactions
c. Production of pharmaceuticals
d. Production of dyes
e. Production of other organic compounds

Reactivity

Versatile chemical properties

Additional Properties

a. Antioxidant properties
b. Colorimetric properties

Industrial and Scientific Applications

Useful in a range of applications due to its antioxidant and colorimetric properties

Upstream product

• 1460-08-8 2-diazocyclohexane-1,3-dione 
• 504-02-9 1,3-cylohexanedione 
• 86396-02-3 2-(phenyl-λ³-iodaneylidene)cyclohexane-1,3-dione 

Downstream Products

• 81003-48-7 1-Hydroxy(1,1'-bicyclohexyl)-2,2',6,6'-tetron 
• 16588-90-2 1.2.3-Tris-phenylhydrazono-cyclohexan 
• 81003-51-2 2-(2,6-Diacetoxyphenyl)-1,3-cyclohexandion 
• 141519-92-8 2,2-dihydroxycyclohexane-1,3-dione 

Relevant articles and documents

Synthesis of 5-(trifluoromethyl)cyclohexane-1,2,3-trione (cVTC): new trifluoromethyl building block

A simple synthesis of 5-(trifluoromethyl)cyclohexane-1,2,3-trione is demonstrated in one step, by reacting 5-(trifluoromethyl)cyclohexane-1,3-dione with cerium(IV)ammonium nitrate (CAN) in methanol. The compound represents a highly functionalized oxygen-r

Displacement of Dinitrogen by Oxygen: A Methodology for the Catalytic Conversion of Diazocarbonyl Compounds to Ketocarbonyl Compounds by 2,6-Dichloropyridine-N-oxide

Dirhodium(II) catalyzed dinitrogen extrusion from diazocarbonyl compounds by 2,6-dichloropyridine-N-oxide forms ketocarbonyl compounds in near-quantitative yields. Reactions occur at room temperature, and the pyridine product does not coordinate with dirhodium(II) to inhibit catalysis. Anhydrous tricarbonyl compounds, as well as dicarbonyl compounds, are conveniently prepared by this methodology, and they have been used in situ for catalytic ene and aldol transformations.

Synthesis of vicinal trioxo compounds by dimethyl dioxirane oxidation of 2-diazo-1,3-dioxo derivatives

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