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N,N-dibenzyl-2-cyano-2-diazoacetamide

Base Information Edit
  • Chemical Name:N,N-dibenzyl-2-cyano-2-diazoacetamide
  • CAS No.:1627142-83-9
  • Molecular Formula:C17H14N4O
  • Molecular Weight:290.324
  • Hs Code.:
  • Mol file:1627142-83-9.mol
N,N-dibenzyl-2-cyano-2-diazoacetamide

Synonyms:N,N-dibenzyl-2-cyano-2-diazoacetamide

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Chemical Property of N,N-dibenzyl-2-cyano-2-diazoacetamide Edit
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Technology Process of N,N-dibenzyl-2-cyano-2-diazoacetamide

There total 2 articles about N,N-dibenzyl-2-cyano-2-diazoacetamide 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
1.1: methanol / 3 h / 20 °C
1.2: 1 h / 0 - 20 °C
2.1: dicyclohexyl-carbodiimide; dmap / dichloromethane / 1 h / 0 - 20 °C
3.1: sodium azide; trifluoromethylsulfonic anhydride; triethylamine / dichloromethane; water / 2 h / 20 °C / 6000.6 Torr
With dmap; sodium azide; trifluoromethylsulfonic anhydride; triethylamine; dicyclohexyl-carbodiimide; In methanol; dichloromethane; water; 3.1: |Regitz Diazo Transfer;
DOI:10.1021/acs.joc.1c01310
Guidance literature:
Multi-step reaction with 3 steps
1.1: methanol / 3 h / 20 °C
1.2: 1 h / 0 - 20 °C
2.1: dicyclohexyl-carbodiimide; dmap / dichloromethane / 1 h / 0 - 20 °C
3.1: sodium azide; trifluoromethylsulfonic anhydride; triethylamine / dichloromethane; water / 2 h / 20 °C / 6000.6 Torr
With dmap; sodium azide; trifluoromethylsulfonic anhydride; triethylamine; dicyclohexyl-carbodiimide; In methanol; dichloromethane; water; 3.1: |Regitz Diazo Transfer;
DOI:10.1021/acs.joc.1c01310
Guidance literature:
With copper acetylacetonate; In 1,2-dichloro-ethane; for 0.5h; Reagent/catalyst; Solvent; chemospecific reaction; Reflux; Inert atmosphere; Green chemistry;
DOI:10.1002/cctc.201400014
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