(E)-1-(4-butylphenyl)-2-(4-ethoxyphenyl)diazene

Base Information

Chemical Name:(E)-1-(4-butylphenyl)-2-(4-ethoxyphenyl)diazene
CAS No.:31401-34-0
Molecular Formula:C₁₈H₂₂N₂O
Molecular Weight:282.385
Hs Code.:
Mol file:31401-34-0.mol

Synonyms:Azobenzene,4-butyl-4'-ethoxy- (8CI); 4-Butyl-4'-ethoxyazobenzene;p-(p-Ethoxyphenylazo)phenylbutane; p-Butyl-p'-ethoxyazobenzene;p-Ethoxy-p'-butylazobenzene

Suppliers and Price of (E)-1-(4-butylphenyl)-2-(4-ethoxyphenyl)diazene

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of (E)-1-(4-butylphenyl)-2-(4-ethoxyphenyl)diazene

Chemical Property:

Vapor Pressure:8.91E-07mmHg at 25°C
Boiling Point:416.9°C at 760 mmHg
Flash Point:166.1°C
Density:1.01g/cm³

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (E)-1-(4-butylphenyl)-2-(4-ethoxyphenyl)diazene

There total 4 articles about (E)-1-(4-butylphenyl)-2-(4-ethoxyphenyl)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:

: 104-13-2
4-Butylaniline

: 31401-34-0
p-ethoxy p'-n-butyl azo benzene

Guidance literature:: Multi-step reaction with 2 steps

1: (i) NaNO₂, aq. HCl, (ii) /BRN= 3597300/

2: aq. NaOH

With sodium hydroxide;
DOI:10.1021/ja00759a011

Reference yield:

: 139-02-6
sodium phenoxide

: 31401-34-0
p-ethoxy p'-n-butyl azo benzene

Guidance literature:: Multi-step reaction with 2 steps

1: (i) NaNO₂, aq. HCl, (ii) /BRN= 3597300/

2: aq. NaOH

With sodium hydroxide;
DOI:10.1021/ja00759a011