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1-(2,4,5-Trimethoxyphenyl)-1-propanol

Base Information
  • Chemical Name:1-(2,4,5-Trimethoxyphenyl)-1-propanol
  • CAS No.:834-93-5
  • Molecular Formula:C12H18 O4
  • Molecular Weight:226.26892
  • Hs Code.:2909499000
  • DSSTox Substance ID:DTXSID00461273
  • Nikkaji Number:J1.579.520D
  • Mol file:834-93-5.mol
1-(2,4,5-Trimethoxyphenyl)-1-propanol

Synonyms:834-93-5;1-(2,4,5-TRIMETHOXYPHENYL)-1-PROPANOL;1-(2,4,5-trimethoxyphenyl)propan-1-ol;Benzenemethanol,a-ethyl-2,4,6-trimethoxy-;SCHEMBL7091158;DTXSID00461273;NHBUFOXGCPTIOH-UHFFFAOYSA-N;AKOS013209578;2,4,5-trimethoxyphenyl-1-hydroxypropane;A915154

Suppliers and Price of 1-(2,4,5-Trimethoxyphenyl)-1-propanol
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
  • AK Scientific
  • 1-(2,4,5-Trimethoxyphenyl)-1-propanol
  • 5g
  • $ 937.00
Total 14 raw suppliers
Chemical Property of 1-(2,4,5-Trimethoxyphenyl)-1-propanol
Chemical Property:
  • PSA:47.92000 
  • LogP:2.15580 
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:226.12050905
  • Heavy Atom Count:16
  • Complexity:198
Purity/Quality:

97% *data from raw suppliers

1-(2,4,5-Trimethoxyphenyl)-1-propanol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC(C1=CC(=C(C=C1OC)OC)OC)O
Technology Process of 1-(2,4,5-Trimethoxyphenyl)-1-propanol

There total 5 articles about 1-(2,4,5-Trimethoxyphenyl)-1-propanol 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:
Guidance literature:
ethyl bromide; With magnesium; In diethyl ether; for 2h;
2,4,6-trimethoxybenzaldehyde; In diethyl ether; toluene; at 20 ℃;
DOI:10.1246/bcsj.77.2231
Guidance literature:
With iodine; In tetrahydrofuran; at 20 ℃; for 2h;
Guidance literature:
With aluminum tri-bromide; In dichloromethane; at 0 - 20 ℃; for 24h; Inert atmosphere;
DOI:10.1039/c4ob02597k
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