2-METHYLNONADECANE

Base Information

• Chemical Name: 2-METHYLNONADECANE
• CAS No.: 1560-86-7
• Molecular Formula: C₂₀H₄₂
• Molecular Weight: 282.553
• Mol file: 1560-86-7.mol

Synonyms:18-Methylnonadecane;2-Methylnonadecane

Chemical Property of 2-METHYLNONADECANE

Chemical Property:

• Vapor Pressure: 0.000334mmHg at 25°C
• Melting Point: 18.3°C
• Refractive Index: 1.4394
• Boiling Point: 329.7°Cat760mmHg
• Flash Point: 120.6°C
• PSA: 0.00000
• Density: 0.786g/cm³
• LogP: 7.90390

Purity/Quality:

98%Min ^*data from raw suppliers

2-METHYLNONADECANE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 2-METHYLNONADECANE

There total 23 articles about 2-METHYLNONADECANE 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: 91.0%

2-isocyano-2-methylnonadecane (72536-52-8) → isoeicosane (1560-86-7,20574-75-8)

Guidance literature:

With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In benzene; for 0.333333h; Heating;

DOI:10.1039/P19800002657

Reference yield: 83.0%

2,2-Dimethyl-nonadecanenitrile (103682-11-7) → isoeicosane (1560-86-7,20574-75-8)

Guidance literature:

With potassium; toluene; perhydrodibenzo-18-crown-6; Ambient temperature;

DOI:10.1016/S0040-4039(00)95137-2

Reference yield: 83.0%

Thioformic acid O-(1,1-dimethyl-octadecyl) ester (82884-53-5) → isoeicosane (1560-86-7,20574-75-8)

Guidance literature:

With tri-n-butyl-tin hydride; In benzene; Heating;

DOI:10.1016/S0040-4039(00)87249-4

upstream raw materials:

2-methyl-nonadec-2-ene

acetone

1-hydroxy-2(1H)-pyridinethione

oxalyl dichloride

Refernces

• 1、 Tolstikov, G. A.,Spivak, A. Yu.,Lomakina, S. I.,Kuchin, A. V.. "SUBSTITUTION REACTIONS INVOLVING ORGAOALUMINUM COMPOUNDS. COMMUNICATION 4. SYNTHESIS OF ALKYL-SUBSTITUTED CYCLOPROPANES VIA THE ALKYLATION OF HOMOALLYLIC ALCOHOL TOSYLATES WITH TRIALKYLALANES". . p. 1012 - 1017. Retrieved 2007/10/02.
• 2、 Barton, Derek H. R.,Crich, David. "A New Method for the Radical Deoxygenation of Tertiary Alcohols". . p. 774 - 775. Retrieved 2007/10/02.