3,5-Octadiene

Base Information

Chemical Name:3,5-Octadiene
CAS No.:7348-75-6
Molecular Formula:C₈H₁₄
Molecular Weight:110.199
Hs Code.:
DSSTox Substance ID:DTXSID801314987
Nikkaji Number:J327.293A,J330.697F,J330.700J

Synonyms:3,5-Octadiene;25001-92-7;trans-3,trans-5-octadiene;(3e,5z)-3,5-octadiene;3,5-Octadiene, (E,E)-;HWXQYUCHSICMAS-KQQUZDAGSA-N;DTXSID801314987;7348-75-6

Suppliers and Price of 3,5-Octadiene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 0 raw suppliers

Chemical Property of 3,5-Octadiene

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:3
Exact Mass:110.109550447
Heavy Atom Count:8
Complexity:66

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC=CC=CCC
Isomeric SMILES:CC/C=C/C=C/CC

Technology Process of 3,5-Octadiene

There total 9 articles about 3,5-Octadiene 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: 50.0%

: 31844-98-1
(E)/(Z)-1-bromo-1-butene

: 7348-75-6,25001-92-7
3,5-Octadiene

Guidance literature:: With [2,2]bipyridinyl; (2,2'-bipyridine)nickel(II) dibromide; In various solvent(s); at 20 ℃; electrochemical reaction, magnesium anode, gold gauze cathode, -1,2 V;
DOI:10.1016/0022-328X(86)80118-8

Reference yield:

: 3710-30-3
1,7-Octadiene

: 7348-75-6,25001-92-7
3,5-Octadiene

: 13643-08-8
2,4-Octadiene

Guidance literature:: bis(cyclopentadienyl)titanium dichloride; lithium aluminium tetrahydride; at 170 ℃; for 5h; Title compound not separated from byproducts;
DOI:10.1055/s-1982-29697