1-(Allyloxy)-2-allylbenzene

Base Information

Chemical Name:1-(Allyloxy)-2-allylbenzene
CAS No.:3383-05-9
Molecular Formula:C12H14O
Molecular Weight:174.243
Hs Code.:2909309090
European Community (EC) Number:682-396-0
DSSTox Substance ID:DTXSID80448007
Nikkaji Number:J522.147A
Wikidata:Q82266922
Mol file:3383-05-9.mol

Synonyms:1-(Allyloxy)-2-allylbenzene;1-prop-2-enoxy-2-prop-2-enylbenzene;3383-05-9;o,o'-diallylphenol;AGN-PC-0NCNXB;SCHEMBL5085750;DTXSID80448007

Suppliers and Price of 1-(Allyloxy)-2-allylbenzene

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
Packaging
price

Total 5 raw suppliers

Chemical Property of 1-(Allyloxy)-2-allylbenzene

Chemical Property:

PSA：9.23000
LogP:2.97990
XLogP3:3.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:174.104465066
Heavy Atom Count:13
Complexity:163

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C=CCC1=CC=CC=C1OCC=C

Technology Process of 1-(Allyloxy)-2-allylbenzene

There total 13 articles about 1-(Allyloxy)-2-allylbenzene 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: 98.0%

: 591-87-7
Allyl acetate

: 1745-81-9
o-Allylphenol

: 3383-05-9
allyl 2-allylphenyl ether

Guidance literature:: With 5%-palladium/activated carbon; potassium carbonate; triphenylphosphine; In water; at 85 - 105 ℃; for 16h; Inert atmosphere;

Reference yield: 84.0%

: 106-95-6
allyl bromide

: 1745-81-9
o-Allylphenol

: 3383-05-9
allyl 2-allylphenyl ether

Guidance literature:: With potassium carbonate; In acetone; for 1h; Reflux;
DOI:10.1002/hlca.202000216

Reference yield: 77.0%

: 106-95-6
allyl bromide

: 151414-76-5
o-(prop-2-enyloxy)phenylboronic acid

: 3383-05-9
allyl 2-allylphenyl ether

Guidance literature:: With dichloro(N-(diphenylphosphino)-N-isopropyl-1,1-diphenylphosphinamine) digold(I); caesium carbonate; In acetonitrile; at 65 ℃; for 18h; chemoselective reaction;
DOI:10.1002/anie.201402924