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Furo[3,2-b]furan-2,5-dione, 3-(4-methoxyphenyl)-6-phenyl-

Base Information Edit
  • Chemical Name:Furo[3,2-b]furan-2,5-dione, 3-(4-methoxyphenyl)-6-phenyl-
  • CAS No.:22628-17-7
  • Molecular Formula:C19H12 O5
  • Molecular Weight:0
  • Hs Code.:
  • Mol file:22628-17-7.mol
Furo[3,2-b]furan-2,5-dione, 3-(4-methoxyphenyl)-6-phenyl-

Synonyms:2,4-Hexadienedioicacid, 3,4-dihydroxy-2-(p-methoxyphenyl)-5-phenyl-, di-g-lactone (7CI); Furo[3,2-b]furan-2,5-dione,3-(p-methoxyphenyl)-6-phenyl- (8CI); 4-Methoxypulvinic acid lactone

Suppliers and Price of Furo[3,2-b]furan-2,5-dione, 3-(4-methoxyphenyl)-6-phenyl-
Supply Marketing:Edit
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 Furo[3,2-b]furan-2,5-dione, 3-(4-methoxyphenyl)-6-phenyl- Edit
Chemical Property:
  • PSA:61.83000 
  • LogP:2.93120 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of Furo[3,2-b]furan-2,5-dione, 3-(4-methoxyphenyl)-6-phenyl-

There total 17 articles about Furo[3,2-b]furan-2,5-dione, 3-(4-methoxyphenyl)-6-phenyl- 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 acetic anhydride; In dimethyl sulfoxide; at 100 ℃; for 0.25h;
Guidance literature:
Multi-step reaction with 9 steps
1: 65 percent / diethyl ether / Ambient temperature; overnight
2: 98 percent / triethylamine / tetrahydrofuran / 0.5 h / 25 °C
3: 73 percent / 1,5-diazabicyclo<5.4.0>undec-5-ene / dimethylformamide / 2 h / -15 °C
4: 97 percent / diethyl ether / 0.5 h / 0 °C
5: 54 percent / bromine / acetic acid / 2 h / Ambient temperature
6: 20 percent / 1,5-diazabicyclo<5.4.0>undec-5-ene / benzene / 0.75 h
7: 1) boron tribromide, 2) conc. aq. hydrochloric acid / 1) dichloromethane, reflux, 30 min, 2) 30 min
8: 82 percent / sodium methoxide / methanol / 0.5 h
9: 62 percent / acetic anhydride / dimethylsulfoxide / 0.25 h / 100 °C
With hydrogenchloride; bromine; sodium methylate; acetic anhydride; boron tribromide; triethylamine; 1,5-Diazabicyclo[5.4.0]undec-5-ene; In tetrahydrofuran; methanol; diethyl ether; acetic acid; dimethyl sulfoxide; N,N-dimethyl-formamide; benzene;
Guidance literature:
Multi-step reaction with 8 steps
1: 98 percent / triethylamine / tetrahydrofuran / 0.5 h / 25 °C
2: 73 percent / 1,5-diazabicyclo<5.4.0>undec-5-ene / dimethylformamide / 2 h / -15 °C
3: 97 percent / diethyl ether / 0.5 h / 0 °C
4: 54 percent / bromine / acetic acid / 2 h / Ambient temperature
5: 20 percent / 1,5-diazabicyclo<5.4.0>undec-5-ene / benzene / 0.75 h
6: 1) boron tribromide, 2) conc. aq. hydrochloric acid / 1) dichloromethane, reflux, 30 min, 2) 30 min
7: 82 percent / sodium methoxide / methanol / 0.5 h
8: 62 percent / acetic anhydride / dimethylsulfoxide / 0.25 h / 100 °C
With hydrogenchloride; bromine; sodium methylate; acetic anhydride; boron tribromide; triethylamine; 1,5-Diazabicyclo[5.4.0]undec-5-ene; In tetrahydrofuran; methanol; diethyl ether; acetic acid; dimethyl sulfoxide; N,N-dimethyl-formamide; benzene;
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