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(E)-4-(3-oxo-3-phenethoxyprop-1-enyl)-1,2-phenylene diacetate

Base Information Edit
  • Chemical Name:(E)-4-(3-oxo-3-phenethoxyprop-1-enyl)-1,2-phenylene diacetate
  • CAS No.:118971-54-3
  • Molecular Formula:C21H20O6
  • Molecular Weight:368.386
  • Hs Code.:
  • Mol file:118971-54-3.mol
(E)-4-(3-oxo-3-phenethoxyprop-1-enyl)-1,2-phenylene diacetate

Synonyms:(E)-4-(3-oxo-3-phenethoxyprop-1-enyl)-1,2-phenylene diacetate

Suppliers and Price of (E)-4-(3-oxo-3-phenethoxyprop-1-enyl)-1,2-phenylene diacetate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 0 raw suppliers
Chemical Property of (E)-4-(3-oxo-3-phenethoxyprop-1-enyl)-1,2-phenylene diacetate Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of (E)-4-(3-oxo-3-phenethoxyprop-1-enyl)-1,2-phenylene diacetate

There total 2 articles about (E)-4-(3-oxo-3-phenethoxyprop-1-enyl)-1,2-phenylene diacetate 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 dmap; dicyclohexyl-carbodiimide; In toluene; at 90 ℃; for 3h; Inert atmosphere;
DOI:10.1016/j.ejmech.2014.01.049
Guidance literature:
Multi-step reaction with 2 steps
1: dmap; pyridine / 2 h / 20 °C / Inert atmosphere
2: dicyclohexyl-carbodiimide; dmap / toluene / 3 h / 90 °C / Inert atmosphere
With pyridine; dmap; dicyclohexyl-carbodiimide; In toluene;
DOI:10.1016/j.ejmech.2014.01.049
Guidance literature:
With pyrrolidine; In tetrahydrofuran; at 20 ℃; for 0.5h;
DOI:10.1016/j.ejmech.2014.01.049
upstream raw materials:

caffeic acid

2-phenylethanol

3,4-diacetoxycinnamic acid

Downstream raw materials:

Caffeic acid phenethyl ester

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