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bis-N,N-(p-nitrophenyl-2,2-diphenylethyl-12-aminododecyl phosphate)-2,5-dimethoxyterephthalamide

Base Information Edit
  • Chemical Name:bis-N,N-(p-nitrophenyl-2,2-diphenylethyl-12-aminododecyl phosphate)-2,5-dimethoxyterephthalamide
  • CAS No.:906072-82-0
  • Molecular Formula:C74H92N4O16P2
  • Molecular Weight:1355.51
  • Hs Code.:
  • Mol file:906072-82-0.mol
bis-N,N-(p-nitrophenyl-2,2-diphenylethyl-12-aminododecyl phosphate)-2,5-dimethoxyterephthalamide

Synonyms:bis-N,N-(p-nitrophenyl-2,2-diphenylethyl-12-aminododecyl phosphate)-2,5-dimethoxyterephthalamide

Suppliers and Price of bis-N,N-(p-nitrophenyl-2,2-diphenylethyl-12-aminododecyl phosphate)-2,5-dimethoxyterephthalamide
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of bis-N,N-(p-nitrophenyl-2,2-diphenylethyl-12-aminododecyl phosphate)-2,5-dimethoxyterephthalamide Edit
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Technology Process of bis-N,N-(p-nitrophenyl-2,2-diphenylethyl-12-aminododecyl phosphate)-2,5-dimethoxyterephthalamide

There total 8 articles about bis-N,N-(p-nitrophenyl-2,2-diphenylethyl-12-aminododecyl phosphate)-2,5-dimethoxyterephthalamide 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:
Multi-step reaction with 3 steps
1: DBU / toluene
2: trifluoroacetic acid / CH2Cl2 / 0.33 h
3: triethylamine / CHCl3 / 3 h
With 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; trifluoroacetic acid; In dichloromethane; chloroform; toluene;
DOI:10.1021/ja0619253
Guidance literature:
Multi-step reaction with 2 steps
1: trifluoroacetic acid / CH2Cl2 / 0.33 h
2: triethylamine / CHCl3 / 3 h
With triethylamine; trifluoroacetic acid; In dichloromethane; chloroform;
DOI:10.1021/ja0619253
Guidance literature:
Multi-step reaction with 4 steps
1: 90 percent / DBU / CHCl3 / 3 h
2: DBU / toluene
3: trifluoroacetic acid / CH2Cl2 / 0.33 h
4: triethylamine / CHCl3 / 3 h
With 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; trifluoroacetic acid; In dichloromethane; chloroform; toluene;
DOI:10.1021/ja0619253
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