4-Ethenylbenzene-1,3-diol

Base Information

Chemical Name:4-Ethenylbenzene-1,3-diol
CAS No.:106209-27-2
Molecular Formula:C₈H₈O₂
Molecular Weight:136.15
Hs Code.:
DSSTox Substance ID:DTXSID101020238
Nikkaji Number:J759.888B
Wikidata:Q103817734
Metabolomics Workbench ID:101334

Synonyms:4-ethenylbenzene-1,3-diol;106209-27-2;4-ethenyl-1,3-benzenediol;4-vinylresorcinol;4-Vinylbenzene-1,3-diol;4-vinyl resorcinol;SCHEMBL686136;DTXSID101020238;EN300-1850232

Suppliers and Price of 4-Ethenylbenzene-1,3-diol

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 19 raw suppliers

Chemical Property of 4-Ethenylbenzene-1,3-diol

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:136.052429494
Heavy Atom Count:10
Complexity:122

Purity/Quality:: 99% ,98%,Electron Grade , ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CC1=C(C=C(C=C1)O)O

Technology Process of 4-Ethenylbenzene-1,3-diol

There total 5 articles about 4-Ethenylbenzene-1,3-diol 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: 72.0%

: 214896-06-7
3-acetoxy-4-vinylphenyl pivalate

: 106209-27-2
4-ethenyl-1,3-benzenediol

Guidance literature:: With n-butyllithium; In tetrahydrofuran; hexane; for 1h; Ambient temperature;
DOI:10.1021/jo980785f

Reference yield:

: 214895-80-4
3-hydroxyphenyl pivalate

: 106209-27-2
4-ethenyl-1,3-benzenediol

Guidance literature:: Multi-step reaction with 2 steps

2: 72 percent / n-BuLi / tetrahydrofuran; hexane / 1 h / Ambient temperature

With n-butyllithium; In tetrahydrofuran; hexane;
DOI:10.1021/jo980785f