2-Hydroxy-6-methyl-5-allylanisole

Base Information

Chemical Name:2-Hydroxy-6-methyl-5-allylanisole
CAS No.:186743-24-8
Molecular Formula:C11H14O2
Molecular Weight:178.22800
Hs Code.:
DSSTox Substance ID:DTXSID80575665
Metabolomics Workbench ID:60393
Nikkaji Number:J833.232K
Wikidata:Q27126442

Synonyms:3-METHYLEUGENOL;2-hydroxy-6-methyl-5-allylanisole;o-methoxy-m-methyl-p-allylphenol;4-allyl-2-methoxy-3-methyl-phenol;186743-24-8;CHEBI:59074;2-methoxy-3-methyl-4-(2-propen-1-yl)-phenol;4-allyl-2-methoxy-3-methylphenol;2-methoxy-3-methyl-4-prop-2-enylphenol;Epitope ID:122689;SCHEMBL132917;DTXSID80575665;Q27126442

Suppliers and Price of 2-Hydroxy-6-methyl-5-allylanisole

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2-Hydroxy-6-methyl-5-allylanisole

Chemical Property:

PSA：29.46000
LogP:2.43770
XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:178.099379685
Heavy Atom Count:13
Complexity:168

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=C(C=CC(=C1OC)O)CC=C

Technology Process of 2-Hydroxy-6-methyl-5-allylanisole

There total 4 articles about 2-Hydroxy-6-methyl-5-allylanisole 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: 76.0%

: 186743-33-9
6-methylallylguaiacol

: 186743-24-8
methyl eugenol

Guidance literature:: at 180 ℃; for 4h;
DOI:10.1021/tx960087v

Reference yield:

: 2896-67-5
2-methyl-6-methoxyphenol

: 186743-24-8
methyl eugenol

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / K₂CO₃ / acetone / 12 h

2: 76 percent / 4 h / 180 °C

With potassium carbonate; In acetone;
DOI:10.1021/tx960087v

Reference yield:

: 148-53-8
3-methoxy-2-hydroxybenzaldehyde

: 186743-24-8
methyl eugenol

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / hydrazine monohydrate; K₂CO₃ / triethylene glycol / 4.5 h / 200 °C / Heating

2: 85 percent / K₂CO₃ / acetone / 12 h

3: 76 percent / 4 h / 180 °C

With potassium carbonate; hydrazine hydrate; In acetone; 2,2'-[1,2-ethanediylbis(oxy)]bisethanol;
DOI:10.1021/tx960087v