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(2E)-N-(diphenylmethyl)-3-phenylprop-2-enamide

Base Information
  • Chemical Name:(2E)-N-(diphenylmethyl)-3-phenylprop-2-enamide
  • CAS No.:853349-32-3
  • Molecular Formula:C22H19NO
  • Molecular Weight:313.399
  • Hs Code.:
  • European Community (EC) Number:662-072-5
  • DSSTox Substance ID:DTXSID90361516
  • Nikkaji Number:J3.563.036H
  • Wikidata:Q76119967
(2E)-N-(diphenylmethyl)-3-phenylprop-2-enamide

Synonyms:853349-32-3;(2E)-N-(diphenylmethyl)-3-phenylprop-2-enamide;ST026373;N-Benzhydryl-3-phenylacrylamide;SCHEMBL18065062;DTXSID90361516;STK020932;AKOS000490815;BIM-0045557.P001;(2E)-N-benzhydryl-3-phenyl-2-propenamide;J3.563.036H

Suppliers and Price of (2E)-N-(diphenylmethyl)-3-phenylprop-2-enamide
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
Total 1 raw suppliers
Chemical Property of (2E)-N-(diphenylmethyl)-3-phenylprop-2-enamide
Chemical Property:
  • XLogP3:4.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:5
  • Exact Mass:313.146664230
  • Heavy Atom Count:24
  • Complexity:380
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C=CC(=O)NC(C2=CC=CC=C2)C3=CC=CC=C3
  • Isomeric SMILES:C1=CC=C(C=C1)/C=C/C(=O)NC(C2=CC=CC=C2)C3=CC=CC=C3
Technology Process of (2E)-N-(diphenylmethyl)-3-phenylprop-2-enamide

There total 3 articles about (2E)-N-(diphenylmethyl)-3-phenylprop-2-enamide 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-Methyl-2-nitropropane; oxygen; trifluoroacetic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; at 20 ℃; for 12h; Irradiation;
Guidance literature:
cinnamic nitrile; 1,1-Diphenylmethanol; With tetrafluoroboric acid diethyl ether; at 20 ℃; for 4h;
With water; sodium hydrogencarbonate; at 20 ℃;
DOI:10.1055/s-0034-1380754
Guidance literature:
Multi-step reaction with 2 steps
1.1: sodium azide; tetrafluoroboric acid diethyl ether; acetic acid / 1 h / 20 °C
2.1: tetrafluoroboric acid diethyl ether / 4 h / 20 °C
2.2: 20 °C
With tetrafluoroboric acid diethyl ether; sodium azide; acetic acid; 1.1: |Schmidt Reaction / 2.1: |Ritter Amidation;
DOI:10.1055/s-0034-1380754
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