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N-Cyano-1-(4-methoxybenzoyl)-2-pyrrolidinimine

Base Information Edit
  • Chemical Name:N-Cyano-1-(4-methoxybenzoyl)-2-pyrrolidinimine
  • CAS No.:159383-34-3
  • Molecular Formula:C13H13N3O2
  • Molecular Weight:243.265
  • Hs Code.:
  • Nikkaji Number:J543.829B
  • Mol file:159383-34-3.mol
N-Cyano-1-(4-methoxybenzoyl)-2-pyrrolidinimine

Synonyms:1-(p-Methoxybenzoyl)-2-cyaniminopyrrolidine;N-Cyano-1-(4-methoxybenzoyl)-2-pyrrolidinimine;2-Pyrrolidinimine, N-cyano-1-(4-methoxybenzoyl)-;159383-34-3;AKOS001669229;LS-138252;EU-0014414;1-(4-Methoxybenzoyl)-N-cyanopyrrolidin-2-imine;SR-01000083944;SR-01000083944-1;1-(4-METHOXYBENZOYL)-2-PYRROLIDINYLIDENECYANAMIDE

Suppliers and Price of N-Cyano-1-(4-methoxybenzoyl)-2-pyrrolidinimine
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 N-Cyano-1-(4-methoxybenzoyl)-2-pyrrolidinimine Edit
Chemical Property:
  • Vapor Pressure:1.45E-06mmHg at 25°C 
  • Boiling Point:398.7°Cat760mmHg 
  • Flash Point:194.9°C 
  • Density:1.21g/cm3 
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:243.100776666
  • Heavy Atom Count:18
  • Complexity:388
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=CC=C(C=C1)C(=O)N2CCCC2=NC#N
Technology Process of N-Cyano-1-(4-methoxybenzoyl)-2-pyrrolidinimine

There total 1 articles about N-Cyano-1-(4-methoxybenzoyl)-2-pyrrolidinimine 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; Yield given. Multistep reaction; 1.) a) toluene reflux 30 min, b) toluene, ethanol, reflux, 3 h, 2.) 5 deg C, overnight;
DOI:10.1007/BF00772851
upstream raw materials:

4-methoxy-benzoyl chloride

Refernces Edit
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