2319-61-1

Basic information

• Product Name: 1-cyclohexylethylcyclohexane
• Synonyms: 1-cyclohexylethylcyclohexane;1,1'-Ethylidenebiscyclohexane;1,1'-Ethylidenedicyclohexane
• CAS NO: 2319-61-1
• Molecular Formula: C₁₄H₂₆
• Molecular Weight: 194.36
• Mol File: 2319-61-1.mol
• Article Data: 7

Chemical Properties

• Melting Point: -20.82°C
• Boiling Point: 271.17°C
• Flash Point: 103.7°C
• Appearance: /
• Density: 0.8897
• Refractive Index: 1.4825
• CAS DataBase Reference: 1-cyclohexylethylcyclohexane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-cyclohexylethylcyclohexane(2319-61-1)
• EPA Substance Registry System: 1-cyclohexylethylcyclohexane(2319-61-1)

Safety Data

• Hazardous Substances Data: 2319-61-1(Hazardous Substances Data)

Usage

Chemical structure

1-cyclohexylethylcyclohexane consists of two cyclohexane rings connected by an ethyl group.

Classification

It is an organic compound due to its carbon-based structure.

Usage

Commonly used in the field of organic chemistry.

Reactivity

Exhibits low reactivity.

Stability

High stability due to its cycloalkane nature.

Solubility

Limited solubility in water.

Applications

Suitable for use as a solvent or in the production of other organic compounds.

Synthesis

Can be used as a starting material in the synthesis of more complex organic molecules.

Versatility

Unique and versatile structure allows for various reactions and synthesis processes.

Upstream product

• 4413-16-5 1-ethyl-4-phenylcyclohexane 
• 612-00-0 1,1'-ethylidenebis-benzene 
• 64-19-7 acetic acid 
• 57013-04-4 ethene-1,1-diyldicyclohexane 
• 2081-08-5 bisphenol E 
• 530-48-3 1,1-Diphenylethylene 
• 1883-32-5 2,2-diphenyl ethanol 
• 53317-13-8 1,1-dicyclohexylethanol 

Relevant articles and documents

Radical-chain deoxygenation of tertiary alcohols, protected as their methoxymethyl (MOM) ethers, using thiols as polarity-reversal catalysts

The deoxygenation of tertiary alcohols can be accomplished by heating their MOM ethers in the presence of a peroxide initiator and a thiol catalyst: the proposed radical-chain mechanism is supported by EPR spectroscopic studies.

Stainless Steel-Mediated Hydrogen Generation from Alkanes and Diethyl Ether and Its Application for Arene Reduction

Hydrogen gas can be generated from simple alkanes (e.g., n-pentane, n-hexane, etc.) and diethyl ether (Et2O) by mechanochemical energy using a planetary ball mill (SUS304, Fritsch Pulverisette 7), and the use of stainless steel balls and vessel is an important factor to generate the hydrogen. The reduction of organic compounds was also accomplished using the in-situ-generated hydrogen. While the use of pentane as the hydrogen source facilitated the reduction of the olefin moieties, the arene reduction could proceed using Et2O. Within the components (Fe, Cr, Ni, etc.) of the stainless steel, Cr was the metal factor for the hydrogen generation from the alkanes and Et2O, and Ni metal played the role of the hydrogenation catalyst.

Br?nsted Acid-Catalyzed Transfer Hydrogenation of Imines and Alkenes Using Cyclohexa-1,4-dienes as Dihydrogen Surrogates

Cyclohexa-1,4-dienes are introduced to Br?nsted acid-catalyzed transfer hydrogenation as an alternative to the widely used Hantzsch dihydropyridines. While these hydrocarbon-based dihydrogen surrogates do offer little advantage over established protocols in imine reduction as well as reductive amination, their use enables the previously unprecedented transfer hydrogenation of structurally and electronically unbiased 1,1-di- and trisubstituted alkenes. The mild procedure requires 5.0 mol % of Tf2NH, but the less acidic sulfonic acids TfOH and TsOH work equally well.