4016-06-2

Basic information

• Product Name: 1,3-Dicyclohexylbenzene
• Synonyms: 1,3-Dicyclohexylbenzene
• CAS NO: 4016-06-2
• Molecular Formula: C₁₈H₂₆
• Molecular Weight: 0
• Mol File: 4016-06-2.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3-Dicyclohexylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dicyclohexylbenzene(4016-06-2)
• EPA Substance Registry System: 1,3-Dicyclohexylbenzene(4016-06-2)

Safety Data

• Hazardous Substances Data: 4016-06-2(Hazardous Substances Data)

Usage

Physical state at room temperature

White, crystalline solid

Solubility in water

Insoluble

Common uses

High-temperature heat transfer fluid in industrial processes
Intermediate for the synthesis of various organic compounds
Lubricant additive
Production of polymers, resins, and specialty chemicals

Boiling point

High (specific value not provided)

Thermal stability

High

Safety precautions

Potential harm if ingested or inhaled
Can cause skin and eye irritation

Upstream product

• 94030-51-0 1-(3-Cyclohexyl-phenyl)-cyclohexen-⁽¹⁾ 
• 931-50-0 cyclohexylmagnesium bromide 
• 541-73-1 1,3-Dichlorobenzene 
• 75879-77-5 2(R^*),6(S^*)-di(1-cyclohexen-1-yl)cyclohexen-1(s^*)-ol 
• 7446-70-0 aluminium trichloride 
• 110-83-8 cyclohexene 
• 71-43-2 benzene 
• 7664-93-9 sulfuric acid 
• 108-94-1 cyclohexanone 
• 827-52-1 1-phenyl-1-cyclohexane 
• 542-18-7 cyclohexyl chloride 
• 24344-21-6 2,6-bis(1-cyclohexenyl)cyclohexanone 
• 95168-30-2 1-(3-Cyclohexyl-phenyl)-cyclohexanol-⁽¹⁾ 
• 1706-50-9 perhydro-meta-terphenyl 

Downstream Products

• 194291-20-8 (3-Amino-phenyl)-(2,4-dicyclohexyl-phenyl)-methanone 

Relevant articles and documents

Benzene Alkylation with Cycloolefins under the Action of [Et3NH]+[Al2Cl7]? Ionic Liquid

Benzene alkylation with mono- and bicyclic olefins under the action of an inorganic ionic liquid [Et3NH]+[Al2Cl7]? with the formation of benzene cycloalkyl derivatives in 58–98% yield has been performed for the first time. It has been found that the increase in the olefin cycle size improves the selectivity with respect to monocycloalkyl derivatives.

PROCESS FOR PRODUCING A MONOCYCLOALKYL-SUBSTITUTED AROMATIC COMPOUND

In a process for producing mono-cycloalkyl-substituted aromatic compound, benzene and cyclic monoolefin are contacted with a catalyst under alkylation conditions to produce an effluent containing mono-cycloalkyl-substituted aromatic compound. The catalyst comprises a molecular sieve.