Cyclotetradecane

Base Information

• Chemical Name: Cyclotetradecane
• CAS No.: 295-17-0
• Molecular Formula: C14H28
• Molecular Weight: 196.376
• European Community (EC) Number: 206-038-6
• UNII: O1MV54BB89
• DSSTox Substance ID: DTXSID70183697
• Nikkaji Number: J129.176I
• Wikipedia: Cyclotetradecane
• Wikidata: Q7485816
• Metabolomics Workbench ID: 46110
• Mol file: 295-17-0.mol

Synonyms:Cyclotetradecane;295-17-0;EINECS 206-038-6;O1MV54BB89;UNII-O1MV54BB89;CHEBI:89715;DTXSID70183697;AKOS006272110;FT-0693190;Q7485816

Chemical Property of Cyclotetradecane

Chemical Property:

• Vapor Pressure: 0.00625mmHg at 25°C
• Melting Point: 55.6°C
• Refractive Index: 1.5500 (estimate)
• Boiling Point: 280.9°Cat760mmHg
• Flash Point: 113.1°C
• PSA: 0.00000
• Density: 0.79g/cm³
• LogP: 5.46140
• XLogP3: 7.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 196.219100893
• Heavy Atom Count: 14
• Complexity: 53.3

Purity/Quality:

99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Other Classes -> Aliphatics, Saturated (>C11)
• Canonical SMILES: C1CCCCCCCCCCCCC1
• Uses: Cyclotetradecane is a chemical constituent of the ethanolic extract of Citrus limon leaves that exhibits anti-microbial properties.

Technology Process of Cyclotetradecane

There total 16 articles about Cyclotetradecane 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: 100.0%

cis-trans-1,8-Cyclotetradecadien (4308-14-9) → cyclotetradecane (295-17-0)

Guidance literature:

With hydrogen; palladium on activated charcoal; In hexane; at 25 ℃;

DOI:10.1055/s-1987-28129

Reference yield: 41.0%

1,2,9,10-tetraoxacyclodocosane-3,8,11,22-tetraone (106051-53-0) → 1-tetradecene (1120-36-1) + cyclotetradecane (295-17-0)

Guidance literature:

at -78 ℃; for 50h; Irradiation;

DOI:10.1016/S0040-4020(01)87347-6

Reference yield: 17.2%

→ cyclotetradecane (295-17-0)

Guidance literature:

upstream raw materials:

cyclotetradeca-1,3-diyne

cyclotetradeca-1,3,8,10-tetrayne

cyclotetradecanone

cis-cyclotetradecene

Downstream raw materials:

phenanthrene

anthracene

Refernces

• 1、 Sondheimer et al.. "-". . . Retrieved 1959.
• 2、 Riache, Nassima,Callens, Emmanuel,Samantaray, Manoja K.,Kharbatia, Najeh M.,Atiqullah, Muhammad,Basset, Jean-Marie. "Cyclooctane metathesis catalyzed by silica-supported tungsten pentamethyl [(ΞSiO)W(Me)5]: Distribution of macrocyclic alkanes". supporting information. p. 15089 - 15094. Retrieved 2015/02/19.