(4-Methoxyphenyl)(2-methylphenyl)diazene

Base Information

Chemical Name:(4-Methoxyphenyl)(2-methylphenyl)diazene
CAS No.:29418-43-7
Molecular Formula:C14H14 N2 O
Molecular Weight:226.278
Hs Code.:
DSSTox Substance ID:DTXSID101233043
Nikkaji Number:J1.614.011B

Synonyms:(4-METHOXYPHENYL)(2-METHYLPHENYL)DIAZENE;29418-43-7;4'-Methoxy-2-methylazobenzene;DTXSID101233043;Diazene, (4-methoxyphenyl)(2-methylphenyl)-, (E)-;31023-30-0

Suppliers and Price of (4-Methoxyphenyl)(2-methylphenyl)diazene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of (4-Methoxyphenyl)(2-methylphenyl)diazene

Chemical Property:

Vapor Pressure:3.21E-05mmHg at 25°C
Boiling Point:365.8°Cat760mmHg
Flash Point:142.1°C
Density:1.05g/cm³
XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:226.110613074
Heavy Atom Count:17
Complexity:247

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=CC=C1N=NC2=CC=C(C=C2)OC

Technology Process of (4-Methoxyphenyl)(2-methylphenyl)diazene

There total 5 articles about (4-Methoxyphenyl)(2-methylphenyl)diazene 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:

Reference yield: 80.0%

: 100-17-4
para-methoxynitrobenzene

: 88-72-2
1-methyl-2-nitrobenzene

: 29418-43-7
(4-methoxy-phenyl)-o-tolyl-diazene

Guidance literature:: With chloro-trimethyl-silane; samarium diiodide; tetra-(n-butyl)ammonium iodide; tert-butylammonium hexafluorophosphate(V); In tetrahydrofuran; at 20 ℃; for 5h; Electrochemical reaction;
DOI:10.1021/acscatal.7b02940