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2,4-dimethoxy-N-phenylaniline

Base Information Edit
  • Chemical Name:2,4-dimethoxy-N-phenylaniline
  • CAS No.:90043-09-7
  • Molecular Formula:C14H15NO2
  • Molecular Weight:229.279
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80545762
  • Nikkaji Number:J195.961A
  • Wikidata:Q82423366
  • Mol file:90043-09-7.mol
2,4-dimethoxy-N-phenylaniline

Synonyms:2,4-dimethoxy-N-phenylaniline;90043-09-7;N-phenyl-2,4-dimethoxyaniline;SCHEMBL10785269;DTXSID80545762;PMGRJBUVIQOZNC-UHFFFAOYSA-N;(2,4-dimethoxy-phenyl)-phenyl-amine;SB79850

Suppliers and Price of 2,4-dimethoxy-N-phenylaniline
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Chemical Property of 2,4-dimethoxy-N-phenylaniline Edit
Chemical Property:
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:229.110278721
  • Heavy Atom Count:17
  • Complexity:216
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COC1=CC(=C(C=C1)NC2=CC=CC=C2)OC
Technology Process of 2,4-dimethoxy-N-phenylaniline

There total 7 articles about 2,4-dimethoxy-N-phenylaniline 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 copper immobilized at polyimide covalent organic framework; In methanol; water; at 20 ℃; for 8h;
DOI:10.1039/c8gc02611d
Guidance literature:
copper(I) acetate; In dichloromethane; for 2h;
DOI:10.1016/S0040-4039(00)99469-3
Guidance literature:
With potassium hydroxide; In dimethyl sulfoxide; at 130 ℃; for 15h;
DOI:10.1007/s10562-018-2580-4
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