Ethylcyclooctane

Base Information

• Chemical Name: Ethylcyclooctane
• CAS No.: 13152-02-8
• Molecular Formula: C10H20
• Molecular Weight: 140.269
• Hs Code.: 2902199090
• DSSTox Substance ID: DTXSID70157095
• Nikkaji Number: J124.798K
• Wikidata: Q83025219
• Mol file: 13152-02-8.mol

Synonyms:ETHYLCYCLOOCTANE;Cyclooctane, ethyl-;13152-02-8;Cyclooctane ethyl-, ethyl-;DTXSID70157095;FBGUQAGGWLRXTP-UHFFFAOYSA-N

Chemical Property of Ethylcyclooctane

Chemical Property:

• Vapor Pressure: 0.986mmHg at 25°C
• Boiling Point: 184.8°Cat760mmHg
• Flash Point: 53.2°C
• PSA: 0.00000
• Density: 0.781g/cm³
• LogP: 3.75690
• XLogP3: 5.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 140.156500638
• Heavy Atom Count: 10
• Complexity: 68.1

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC1CCCCCCC1

Technology Process of Ethylcyclooctane

There total 3 articles about Ethylcyclooctane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 32.0%

ethene (74-85-1) + Cyclooctan (292-64-8) → cis-Cyclooctene (931-88-4,931-87-3,25267-51-0) + ethyl-cyclooctane (13152-02-8) + vinyl cyclooctane (61142-41-4)

Guidance literature:

RhCl(CH₂=CH₂)(PMe₃)2; at 230 ℃; for 15h; under 22800 Torr; Product distribution; also at 170 deg C, different pressures;

DOI:10.1246/cl.1991.359

Reference yield:

Cyclooctan (292-64-8) → cis-Cyclooctene (931-88-4,931-87-3,25267-51-0) + ethyl-cyclooctane (13152-02-8) + vinyl cyclooctane (61142-41-4)

Guidance literature:

With ethene; RhCl(CH₂=CH₂)(PMe₃)2; at 230 ℃; for 15h; under 22800 Torr; Further byproducts given;

DOI:10.1246/cl.1991.359

Reference yield:

ethene (74-85-1) + Cyclooctan (292-64-8) → cis-Cyclooctene (931-88-4,931-87-3,25267-51-0) + ethyl-cyclooctane (13152-02-8) + vinyl cyclooctane (61142-41-4)

Guidance literature:

RhCl(CH₂=CH₂)(PMe₃)2; at 230 ℃; for 15h; under 53200 Torr; Further byproducts given;

DOI:10.1246/cl.1991.359

upstream raw materials:

ethene

Cyclooctan

Refernces