Cyclopropane, tris(1-methylethylidene)-

Base Information

• Chemical Name: Cyclopropane, tris(1-methylethylidene)-
• CAS No.: 2799-44-2
• Molecular Formula: C₁₂H₁₈
• Molecular Weight: 162.275
• DSSTox Substance ID: DTXSID90182268
• Nikkaji Number: J1.108.521K
• Wikidata: Q83052918
• Mol file: 2799-44-2.mol

Synonyms:triisopropylidenecyclopropane;Cyclopropane, tris(1-methylethylidene)-;2799-44-2;Cyclopropane,tris(1-methylethylidene)-;Cyclopropane, triisopropylidene-;DTXSID90182268;1,2,3-Triisopropylidenecyclopropane

Chemical Property of Cyclopropane, tris(1-methylethylidene)-

Chemical Property:

• Vapor Pressure: 0.212mmHg at 25°C
• Boiling Point: 215.8°Cat760mmHg
• Flash Point: 71.1°C
• PSA: 0.00000
• Density: 0.907g/cm³
• LogP: 4.00920
• XLogP3: 3.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 162.140850574
• Heavy Atom Count: 12
• Complexity: 233

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=C1C(=C(C)C)C1=C(C)C)C

Technology Process of Cyclopropane, tris(1-methylethylidene)-

There total 2 articles about Cyclopropane, tris(1-methylethylidene)- 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:

1,1-dibromo-2-methylpropene (13353-06-5) + 2,5-dimethyl-2,3,4-hexatriene (2431-31-4) → Triisopropylidencyclopropan (2799-44-2)

Guidance literature:

Multistep reaction; (i) nBuLi, (ii) /BRN= 1734681/;

DOI:10.1016/0040-4020(67)85004-X

Reference yield:

→ Triisopropylidencyclopropan (2799-44-2)

Guidance literature:

1,1-Dibrom-2-methyl-propen, Butyllithium, Tetrahydrofuran (neben 1,1-Dimethyl-2-<2-methyl-isopropenyliden>-3-isopropyliden-cyclopropan);

upstream raw materials:

1,1-dibromo-2-methylpropene

2,5-dimethyl-2,3,4-hexatriene