Etrogol

Base Information

Chemical Name:Etrogol
CAS No.:119417-97-9
Molecular Formula:C13H18 O2
Molecular Weight:206.285
Hs Code.:
DSSTox Substance ID:DTXSID601258614
Nikkaji Number:J1.945.142I
Wikidata:Q27138418
Metabolomics Workbench ID:48429
ChEMBL ID:CHEMBL451598
Mol file:119417-97-9.mol

Synonyms:Etrogol;CHEBI:70079;CHEMBL451598;SCHEMBL18265493;2-[4-(Prenyloxy)phenyl]ethanol;DTXSID601258614;4-(3-Methyl-2-butenyloxy)benzeneethanol;4-[(3-Methyl-2-buten-1-yl)oxy]benzeneethanol;Q27138418;2-{4-[(3-methylbut-2-en-1-yl)oxy]phenyl}ethan-1-ol;119417-97-9

Suppliers and Price of Etrogol

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 0 raw suppliers

Chemical Property of Etrogol

Chemical Property:

PSA：29.46000
LogP:2.56640
XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:206.130679813
Heavy Atom Count:15
Complexity:187

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CCOC1=CC=C(C=C1)CCO)C

Technology Process of Etrogol

There total 2 articles about Etrogol 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: 93.0%

: 501-94-0
p-hydroxyphenethyl alcohol

: 870-63-3
prenyl bromide

: 119417-97-9
Etrogol

Guidance literature:: With potassium carbonate; In acetone; for 1h; Reflux;
DOI:10.1016/j.bmcl.2012.03.057

Reference yield:

: 156-38-7
4-hydroxyphenylacetate

: 119417-97-9
Etrogol

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / sodium borohydride; iodine / tetrahydrofuran / 2 h / Heating

2: 62 percent / potassium carbonate / acetone / 4 h / Heating

With sodium tetrahydroborate; iodine; potassium carbonate; In tetrahydrofuran; acetone;