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2,4-Diethoxybenzyl alcohol

Base Information
  • Chemical Name:2,4-Diethoxybenzyl alcohol
  • CAS No.:181819-52-3
  • Molecular Formula:C11H16O3
  • Molecular Weight:196.246
  • Hs Code.:
  • European Community (EC) Number:621-113-7
  • DSSTox Substance ID:DTXSID00584178
  • Nikkaji Number:J2.137.101G
  • Wikidata:Q82475812
  • Mol file:181819-52-3.mol
2,4-Diethoxybenzyl alcohol

Synonyms:2,4-Diethoxybenzyl alcohol;(2,4-Diethoxyphenyl)methanol;181819-52-3;2 4-DIETHOXYBENZYL ALCOHOL;SCHEMBL6784748;DTXSID00584178;GVURYEOXXOUZQP-UHFFFAOYSA-N;AKOS000348550;CS-0378511

Suppliers and Price of 2,4-Diethoxybenzyl alcohol
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
  • American Custom Chemicals Corporation
  • 2 4-DIETHOXYBENZYL ALCOHOL 95.00%
  • 5MG
  • $ 504.43
Total 4 raw suppliers
Chemical Property of 2,4-Diethoxybenzyl alcohol
Chemical Property:
  • Melting Point:64-68 °C(lit.)
     
  • Refractive Index:1.512 
  • PSA:38.69000 
  • LogP:1.97630 
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:196.109944368
  • Heavy Atom Count:14
  • Complexity:150
Purity/Quality:

98%+ *data from raw suppliers

2 4-DIETHOXYBENZYL ALCOHOL 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xi 
  • Statements: 36 
  • Safety Statements: 26 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC1=CC(=C(C=C1)CO)OCC
Technology Process of 2,4-Diethoxybenzyl alcohol

There total 2 articles about 2,4-Diethoxybenzyl alcohol 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:
With methanol; sodium tetrahydroborate; In tetrahydrofuran; at 100 ℃; for 4.5h;
DOI:10.1016/j.bioorg.2020.104239
Guidance literature:
Multi-step reaction with 2 steps
1.1: potassium carbonate; potassium iodide / acetone / 0.5 h / 50 °C
1.2: 12 h / 80 - 85 °C
2.1: sodium tetrahydroborate; methanol / tetrahydrofuran / 4.5 h / 100 °C
With methanol; sodium tetrahydroborate; potassium carbonate; potassium iodide; In tetrahydrofuran; acetone; 1.1: |Williamson Ether Synthesis;
DOI:10.1016/j.bioorg.2020.104239
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