Phenol, 3,5-dimethoxy-2-(2-propenyl)-

Base Information

Chemical Name:Phenol, 3,5-dimethoxy-2-(2-propenyl)-
CAS No.:32977-07-4
Molecular Formula:C11H14O3
Molecular Weight:194.23
Hs Code.:
DSSTox Substance ID:DTXSID70453827
Nikkaji Number:J1.283.925A
Wikidata:Q82275084

Synonyms:32977-07-4;2-Allyl-3,5-dimethoxyphenol;Phenol, 3,5-dimethoxy-2-(2-propenyl)-;SCHEMBL7828001;DTXSID70453827;AKOS011655262

Suppliers and Price of Phenol, 3,5-dimethoxy-2-(2-propenyl)-

Supply Marketing:

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

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Chemical Property of Phenol, 3,5-dimethoxy-2-(2-propenyl)-

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:194.094294304
Heavy Atom Count:14
Complexity:181

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC(=C(C(=C1)OC)CC=C)O

Technology Process of Phenol, 3,5-dimethoxy-2-(2-propenyl)-

There total 2 articles about Phenol, 3,5-dimethoxy-2-(2-propenyl)- 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: 100.0%

: 32977-06-3
1-(allyloxy)-3,5-dimethoxybenzene

: 32977-07-4
2-allyl-3,5-dimethoxyphenol

Guidance literature:: at 200 ℃; for 0.75h; Inert atmosphere;
DOI:10.3987/COM-13-12744

Reference yield:

: 500-99-2
3,5-dimethoxyphenol

: 32977-07-4
2-allyl-3,5-dimethoxyphenol

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / K₂CO₃ / acetone

2: 75 percent / N,N-dimethylaniline / 7 h / 200 °C

With potassium carbonate; N,N-dimethyl-aniline; In acetone;
DOI:10.1016/S0040-4039(00)96289-0