Phenol, 2,4-dimethoxy-6-(1-methyl-2-propenyl)-

Base Information

Chemical Name:Phenol, 2,4-dimethoxy-6-(1-methyl-2-propenyl)-
CAS No.:181356-76-3
Molecular Formula:C12H16O3
Molecular Weight:208.257
Hs Code.:
DSSTox Substance ID:DTXSID60448065
Nikkaji Number:J1.857.241I
Mol file:181356-76-3.mol

Synonyms:181356-76-3;Phenol, 2,4-dimethoxy-6-(1-methyl-2-propenyl)-;DTXSID60448065;2-(1-Methyl-2-propenyl)-4,6-dimethoxyphenol

Suppliers and Price of Phenol, 2,4-dimethoxy-6-(1-methyl-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, 2,4-dimethoxy-6-(1-methyl-2-propenyl)-

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:208.109944368
Heavy Atom Count:15
Complexity:205

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Phenol, 2,4-dimethoxy-6-(1-methyl-2-propenyl)-

There total 3 articles about Phenol, 2,4-dimethoxy-6-(1-methyl-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: 85.0%

: 1-[((E)-But-2-enyl)oxy]-2,4-dimethoxy-benzene

: 181356-76-3
2,4-dimethoxy-6-(1-methylallyl)phenol

Guidance literature:: With N,N-dimethyl-aniline; at 220 ℃; for 4h;

Reference yield:

: 13330-65-9
2,4-dimethoxyphenol

: 181356-76-3
2,4-dimethoxy-6-(1-methylallyl)phenol

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃ / acetone / 60 °C

2: Heating

With potassium carbonate; In acetone; 2: Claisen rearrangement;
DOI:10.1016/j.tet.2005.08.020