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2-{[(2,4-Dimethoxyphenyl)methyl]amino}-N-phenylbenzamide

Base Information Edit
  • Chemical Name:2-{[(2,4-Dimethoxyphenyl)methyl]amino}-N-phenylbenzamide
  • CAS No.:139602-64-5
  • Molecular Formula:C22H22N2O3
  • Molecular Weight:362.428
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30566902
  • Wikidata:Q82452671
  • Mol file:139602-64-5.mol
2-{[(2,4-Dimethoxyphenyl)methyl]amino}-N-phenylbenzamide

Synonyms:139602-64-5;2-{[(2,4-Dimethoxyphenyl)methyl]amino}-N-phenylbenzamide;DTXSID30566902

Suppliers and Price of 2-{[(2,4-Dimethoxyphenyl)methyl]amino}-N-phenylbenzamide
Supply Marketing:Edit
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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Total 0 raw suppliers
Chemical Property of 2-{[(2,4-Dimethoxyphenyl)methyl]amino}-N-phenylbenzamide Edit
Chemical Property:
  • XLogP3:4.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:7
  • Exact Mass:362.16304257
  • Heavy Atom Count:27
  • Complexity:453
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=CC(=C(C=C1)CNC2=CC=CC=C2C(=O)NC3=CC=CC=C3)OC
Technology Process of 2-{[(2,4-Dimethoxyphenyl)methyl]amino}-N-phenylbenzamide

There total 3 articles about 2-{[(2,4-Dimethoxyphenyl)methyl]amino}-N-phenylbenzamide 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 sodium tetrahydroborate; In ethanol; for 2h; Ambient temperature;
DOI:10.1007/BF00772940
Guidance literature:
Multi-step reaction with 2 steps
1: 96 percent / ethanol / 0.5 h / Ambient temperature
2: 81 percent / sodium borohydride / ethanol / 2 h / Ambient temperature
With sodium tetrahydroborate; In ethanol;
DOI:10.1007/BF00772940
Guidance literature:
Multi-step reaction with 2 steps
1: 96 percent / ethanol / 0.5 h / Ambient temperature
2: 81 percent / sodium borohydride / ethanol / 2 h / Ambient temperature
With sodium tetrahydroborate; In ethanol;
DOI:10.1007/BF00772940
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