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2-(2-Ethylphenyl)acetic acid

Base Information
  • Chemical Name:2-(2-Ethylphenyl)acetic acid
  • CAS No.:19418-95-2
  • Molecular Formula:C10H12O2
  • Molecular Weight:164.204
  • Hs Code.:
  • European Community (EC) Number:837-675-3
  • Nikkaji Number:J599.019J
2-(2-Ethylphenyl)acetic acid

Synonyms:2-(2-ethylphenyl)acetic acid;19418-95-2;2-ethylphenylacetic acid;ethyl benzeneacetic acid;ethylbenzene-acetic acid;2-(2-ethylphenyl)aceticacid;SCHEMBL509855;IDWCPOOBGCOZAY-UHFFFAOYSA-N;AKOS006312840;CS-0309239;EN300-170550;Z1198264425

Suppliers and Price of 2-(2-Ethylphenyl)acetic acid
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 3 raw suppliers
Chemical Property of 2-(2-Ethylphenyl)acetic acid
Chemical Property:
  • XLogP3:2.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:164.083729621
  • Heavy Atom Count:12
  • Complexity:154
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCC1=CC=CC=C1CC(=O)O
Technology Process of 2-(2-Ethylphenyl)acetic acid

There total 9 articles about 2-(2-Ethylphenyl)acetic acid 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 potassium hydroxide; silver nitrate; In ethanol; water;
Guidance literature:
With potassium hydroxide; In ethanol; at 20 ℃; for 15h;
DOI:10.1002/ejoc.201601354
Guidance literature:
Multi-step reaction with 3 steps
1.1: bromine; N-ethyl-N,N-diisopropylamine / dichloromethane / 0.08 h / 0 °C / Inert atmosphere; Cooling with ice
1.2: 20 °C / Inert atmosphere
2.1: potassium tert-butylate / N,N-dimethyl-formamide / 15 h / 155 °C / Inert atmosphere
3.1: potassium hydroxide / ethanol / 15 h / 20 °C
With potassium tert-butylate; bromine; N-ethyl-N,N-diisopropylamine; potassium hydroxide; In ethanol; dichloromethane; N,N-dimethyl-formamide; 2.1: |Claisen Rearrangement;
DOI:10.1002/ejoc.201601354
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