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2-Propenoic acid, 3-(4-methoxyphenyl)-, ethyl ester, (Z)-

Base Information
  • Chemical Name:2-Propenoic acid, 3-(4-methoxyphenyl)-, ethyl ester, (Z)-
  • CAS No.:51507-22-3
  • Molecular Formula:C12H14O3
  • Molecular Weight:206.241
  • Hs Code.:
  • Mol file:51507-22-3.mol
2-Propenoic acid, 3-(4-methoxyphenyl)-, ethyl ester, (Z)-

Synonyms:ethyl (Z)-3-(4-methoxyphenyl)prop-2-enoate;(Z)-3-(4-Methoxy-phenyl)-acrylic acid ethyl ester;(Z)-3-(4-methoxyphenyl)-2-propenoic acid ethyl ester;(Z)-ethyl 3-(4-methoxyphenyl)-2-propenoate;3-(4'-methoxyphenyl)-(Z)-propenoic acid ethyl ester;ethyl (Z)-3-(4-methoxyphenyl)-2-propenoate;ethyl (Z)-3-(4-methoxyphenyl)-prop-2-enoate;

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Chemical Property of 2-Propenoic acid, 3-(4-methoxyphenyl)-, ethyl ester, (Z)-
Chemical Property:
  • Boiling Point:110 - 112 °C 
  • PSA:35.53000 
  • Density:1.080±0.06 g/cm3(Predicted) 
  • LogP:2.27150 
Purity/Quality:
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MSDS Files:

SDS file from LookChem

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Technology Process of 2-Propenoic acid, 3-(4-methoxyphenyl)-, ethyl ester, (Z)-

There total 71 articles about 2-Propenoic acid, 3-(4-methoxyphenyl)-, ethyl ester, (Z)- 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 carbonate; In ethanol; diastereoselective reaction; Milling;
DOI:10.1039/c2gc35669d
Guidance literature:
With triphenylphosphine; In toluene; at 80 ℃; for 6h; optical yield given as %de; stereoselective reaction; Inert atmosphere;
DOI:10.1002/adsc.201100289
Guidance literature:
4-Methoxybenzyl alcohol; With 1,10-Phenanthroline; potassium tert-butylate; copper(l) chloride; In fluorobenzene; at 20 ℃; for 0.166667h; Inert atmosphere;
With 1-methyl-1H-imidazole; di-tert-butyl-diazodicarboxylate; oxygen; In fluorobenzene; Reflux;
diazoacetic acid ethyl ester; With triphenylphosphine; In fluorobenzene; optical yield given as %de; stereoselective reaction; Inert atmosphere;
DOI:10.1021/ol802299d
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