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2,4-Dimethyltridecane

Base Information
  • Chemical Name:2,4-Dimethyltridecane
  • CAS No.:61868-05-1
  • Molecular Formula:61868-05-1
  • Molecular Weight:0
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10455820
  • Nikkaji Number:J2.088.156I
  • Metabolomics Workbench ID:5374
2,4-Dimethyltridecane

Synonyms:2,4-dimethyltridecane;Tridecane, 2,4-dimethyl-;2,4-Dimethyltridecan;61868-05-1;2,4-dimethyl-tridecane;DTXSID10455820;LMFA11000679

Suppliers and Price of 2,4-Dimethyltridecane
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2,4-Dimethyltridecane
Chemical Property:
  • Vapor Pressure:0.024mmHg at 25°C 
  • Boiling Point:257.263°C at 760 mmHg 
  • Flash Point:197.2°C 
  • Density:0.767g/cm3 
  • XLogP3:7.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:10
  • Exact Mass:212.250401021
  • Heavy Atom Count:15
  • Complexity:115
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCCC(C)CC(C)C
Technology Process of 2,4-Dimethyltridecane

There total 5 articles about 2,4-Dimethyltridecane 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:
Guidance literature:
With triethylsilane; In dichloromethane; at 20 ℃; for 1h;
DOI:10.1002/(SICI)1521-3773(19991216)38:24<3675::AID-ANIE3675>3.0.CO;2-I
Guidance literature:
With triethylsilane; triethyl aluminum sesquichloride; In dichloromethane; at -15 - 20 ℃; for 2h;
DOI:10.1021/ja048904y
Guidance literature:
With diethyl ether; Erhitzen des Reaktionsprodukts mit Aluminiumoxid bei 280 und Hydrieren des erhaltenen Olefin-Gemisches an Raney-Nickel bei 150grad/100 at;
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