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1,3-Bis(2-(methoxycarbonyl)phenyl)urea

Base Information
  • Chemical Name:1,3-Bis(2-(methoxycarbonyl)phenyl)urea
  • CAS No.:51364-45-5
  • Molecular Formula:C17H16N2O5
  • Molecular Weight:328.324
  • Hs Code.:
  • European Community (EC) Number:665-063-4
1,3-Bis(2-(methoxycarbonyl)phenyl)urea

Synonyms:1,3-BIS(2-(METHOXYCARBONYL)PHENYL)UREA;AKOS024336182;Methyl 2-({[2-(methoxycarbonyl)phenyl]carbamoyl}amino)benzoate

Suppliers and Price of 1,3-Bis(2-(methoxycarbonyl)phenyl)urea
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
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  • price
Total 1 raw suppliers
Chemical Property of 1,3-Bis(2-(methoxycarbonyl)phenyl)urea
Chemical Property:
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:6
  • Exact Mass:328.10592162
  • Heavy Atom Count:24
  • Complexity:428
Purity/Quality:

98% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COC(=O)C1=CC=CC=C1NC(=O)NC2=CC=CC=C2C(=O)OC
Technology Process of 1,3-Bis(2-(methoxycarbonyl)phenyl)urea

There total 11 articles about 1,3-Bis(2-(methoxycarbonyl)phenyl)urea 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 diphenyl phosphoryl azide; triethylamine; In toluene; for 2h; Reflux;
DOI:10.1055/s-0040-1706643
Guidance literature:
With aluminium trichloride; Yield given. Multistep reaction. Further byproducts given. Yields of byproduct given; 1) ethylene chloride, 1 h 2) ethylene chloride, MeOH, 45 min;
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