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Benzeneacetic acid, 3,4-dimethoxy-2-(phenylmethoxy)-

Base Information Edit
  • Chemical Name:Benzeneacetic acid, 3,4-dimethoxy-2-(phenylmethoxy)-
  • CAS No.:79659-43-1
  • Molecular Formula:C17H18O5
  • Molecular Weight:302.327
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60361649
  • Wikidata:Q82144068
  • Mol file:79659-43-1.mol
Benzeneacetic acid, 3,4-dimethoxy-2-(phenylmethoxy)-

Synonyms:Benzeneacetic acid, 3,4-dimethoxy-2-(phenylmethoxy)-;79659-43-1;DTXSID60361649

Suppliers and Price of Benzeneacetic acid, 3,4-dimethoxy-2-(phenylmethoxy)-
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Benzeneacetic acid, 3,4-dimethoxy-2-(phenylmethoxy)- Edit
Chemical Property:
  • XLogP3:2.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:7
  • Exact Mass:302.11542367
  • Heavy Atom Count:22
  • Complexity:340
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COC1=C(C(=C(C=C1)CC(=O)O)OCC2=CC=CC=C2)OC
Technology Process of Benzeneacetic acid, 3,4-dimethoxy-2-(phenylmethoxy)-

There total 4 articles about Benzeneacetic acid, 3,4-dimethoxy-2-(phenylmethoxy)- 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 hydrogenchloride; potassium hydroxide; In ethanol; water; for 9h; Heating;
DOI:10.1248/cpb.33.5316
Guidance literature:
With hydrogenchloride; sodium methylate; thallium(III) nitrate; Yield given. Multistep reaction; 1.) methylene chloride, room temperature, 1 h; 2.) methanol, H2O, overnight;
DOI:10.1002/jhet.5570180410
Guidance literature:
Multi-step reaction with 2 steps
1: 6.4 g / K2CO3 / acetone / Heating; overnight
2: 1.) Tl(NO3)3 on Montmorillinite clay; 2.) sodium methoxide; aq. HCl / 1.) methylene chloride, room temperature, 1 h; 2.) methanol, H2O, overnight
With hydrogenchloride; sodium methylate; potassium carbonate; thallium(III) nitrate; In acetone;
DOI:10.1002/jhet.5570180410
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