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4-(4-METHOXYPHENYL)-2-AZETIDINONE

Base Information
  • Chemical Name:4-(4-METHOXYPHENYL)-2-AZETIDINONE
  • CAS No.:180264-44-2
  • Molecular Formula:C10H11NO2
  • Molecular Weight:0.00000
  • Hs Code.:
  • Mol file:180264-44-2.mol
4-(4-METHOXYPHENYL)-2-AZETIDINONE

Synonyms:

Suppliers and Price of 4-(4-METHOXYPHENYL)-2-AZETIDINONE
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
  • Acrotein
  • 4-(4-Methoxyphenyl)-2-azetidinone 97%
  • 0.5g
  • $ 302.50
  • Acrotein
  • 4-(4-Methoxyphenyl)-2-azetidinone 97%
  • 1g
  • $ 458.33
Total 3 raw suppliers
Chemical Property of 4-(4-METHOXYPHENYL)-2-AZETIDINONE
Chemical Property:
  • PSA:0.00000 
  • LogP:0.00000 
Purity/Quality:

95%-98% *data from raw suppliers

4-(4-Methoxyphenyl)-2-azetidinone 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 4-(4-METHOXYPHENYL)-2-AZETIDINONE

There total 14 articles about 4-(4-METHOXYPHENYL)-2-AZETIDINONE 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 2,2'-azobis(isobutyronitrile); tris-(trimethylsilyl)silane; In toluene; at 100 ℃; for 2h;
DOI:10.1021/ol005633x
Guidance literature:
With C18H14ClN; N-ethyl-N,N-diisopropylamine; In tert-Amyl alcohol; at 0 ℃; for 30h; optical yield given as %ee; enantioselective reaction;
DOI:10.1021/ol201911z
Guidance literature:
With C18H14ClN; N-ethyl-N,N-diisopropylamine; In tert-Amyl alcohol; at 0 ℃; for 30h; optical yield given as %ee; enantioselective reaction;
DOI:10.1021/ol201911z
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