23391-99-3

Basic information

• Product Name: 4,4'-BICYCLOHEXANONE
• Synonyms: 4,4'-BICYCLOHEXANONE;4,4'-DIOXOBICYCLOHEXYL;[1,1'-Bicyclohexyl]-4,4'-dione;1,1'-Bicyclohexane-4,4'-dione
• CAS NO: 23391-99-3
• Molecular Formula: C₁₂H₁₈O₂
• Molecular Weight: 194.27
• Mol File: 23391-99-3.mol
• Article Data: 4

Chemical Properties

• Melting Point: 118 °C
• Boiling Point: 327.8±42.0℃ (760 Torr)
• Flash Point: 122.9±24.9℃
• Appearance: /
• Density: 1.081±0.06 g/cm3 (20 ºC 760 Torr)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 4,4'-BICYCLOHEXANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4'-BICYCLOHEXANONE(23391-99-3)
• EPA Substance Registry System: 4,4'-BICYCLOHEXANONE(23391-99-3)

Safety Data

• Safety Statements: 24/25
• Hazardous Substances Data: 23391-99-3(Hazardous Substances Data)

Usage

General Description

4,4'-BICYCLOHEXANONE is a chemical compound with the molecular formula C12H18O. It is a cyclic ketone that consists of two cyclohexanone rings linked together through a carbon-carbon bond. 4,4'-BICYCLOHEXANONE is commonly used in organic synthesis and as a building block for the preparation of various pharmaceuticals and fine chemicals. It is also used as a solvent for resins, cellulose ethers, and cellulose acetate. 4,4'-BICYCLOHEXANONE has potential industrial applications due to its high boiling point and stability, making it useful in the production of adhesives, coatings, and other industrial products. Additionally, it is a versatile intermediate in the manufacturing of fragrances, flavors, and other specialty chemicals.

Upstream product

• 92-88-6 4,4'-Dihydroxybiphenyl 
• 21326-53-4 sulfur(IV) oxide * pyridine 
• 63049-36-5 4',4'-Dimethoxy-4-methylsulfanyl-bicyclohexyl-4-carboxylic acid methyl ester 
• 46310-14-9 4,4'-e,e-cyclohexylcyclohexanediol 
• 64-19-7 acetic acid 
• 101-84-8 diphenylether 
• 64554-52-5 1,1'-Bicyclohexylidene-4,4'-dione 
• 20601-38-1 4,4′-dihydroxybicyclohexyl 

Downstream Products

• 109367-22-8 2',3'',2''''',3''''''-tetramethoxy-[1,1';4',1'';4'',1''';4''',1'''';4'''',1''''';4''''',1'''''';4'''''',1''''''']octiphenyl 
• 65181-78-4 4,4'-bis(m-tolylphenylamino)biphenyl 
• 189387-84-6 trans-[1,1'-bi(cyclohexane)]-4,4'-dicarbaldehyde 
• 1246852-59-4 C₂₄H₄₀B₂O₄ 
• 6492-07-5 bicyclohexyl-4,4'-diyldiamine 
• 891828-79-8 4,4'-dimethoxymethylidene bicyclohexane 
• 3598-30-9 3,4,3′,4′-tetrahydroxy-1,1′-biphenyl 
• 179523-43-4 4,4’-bioxepanyl-7,7’-dione 
• 56309-94-5 8-(4-oxocyclohexyl)-1,4-dioxaspiro[4.5]decane 
• 1246852-58-3 C₁₄H₁₆F₆O₆S₂ 
• 214202-82-1 4,4'-dipropylidenebicyclohexyl 

Relevant articles and documents

Photochemical Transformations with Iodine Azide after Release from an Ion-Exchange Resin

This report discloses the photochemical homolytic cleavage of iodine azide after its formation following release from polymer-bound bisazido iodate(I) anions. A series of radical reactions are reported including the 1,2-functionlization of alkenes and the unprecedented chemoselective oxidation of secondary alcohols in the presence of primary alcohols.

Process for the preparation of cyclohexanones

The invention relates to a process for the preparation of cyclohexanones from the corresponding phenols by partial hydrogenation, characterized in that the reaction mixture obtained by means of the hydrogenation is treated with sulfonating agents before the isolation of the cyclohexanone.