{4-[4-(4-Dodecyloxy-phenyl-ONN-azoxy)-phenoxy]-butyl}-trimethyl-ammonium; bromide

Base Information

Chemical Name:{4-[4-(4-Dodecyloxy-phenyl-ONN-azoxy)-phenoxy]-butyl}-trimethyl-ammonium; bromide
CAS No.:78435-07-1
Molecular Formula:Br*C₃₁H₅₀N₃O₃
Molecular Weight:592.66
Hs Code.:

Synonyms:{4-[4-(4-Dodecyloxy-phenyl-ONN-azoxy)-phenoxy]-butyl}-trimethyl-ammonium; bromide

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Chemical Property of {4-[4-(4-Dodecyloxy-phenyl-ONN-azoxy)-phenoxy]-butyl}-trimethyl-ammonium; bromide

Chemical Property:

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Technology Process of {4-[4-(4-Dodecyloxy-phenyl-ONN-azoxy)-phenoxy]-butyl}-trimethyl-ammonium; bromide

There total 5 articles about {4-[4-(4-Dodecyloxy-phenyl-ONN-azoxy)-phenoxy]-butyl}-trimethyl-ammonium; bromide 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: 51.0%

: 78435-35-5
N-[4-(4-Bromo-butoxy)-phenyl]-N'-(4-dodecyloxy-phenyl)-diazene N'-oxide

: 75-50-3
trimethylamine

: 78435-07-1
{4-[4-(4-Dodecyloxy-phenyl-ONN-azoxy)-phenoxy]-butyl}-trimethyl-ammonium; bromide

Guidance literature:: In ethanol;
DOI:10.1021/ja00408a021

Reference yield:

: 65039-19-2
4-(dodecyloxy)aniline

: 78435-07-1
{4-[4-(4-Dodecyloxy-phenyl-ONN-azoxy)-phenoxy]-butyl}-trimethyl-ammonium; bromide

Guidance literature:: Multi-step reaction with 5 steps

1: NaNO₂, HCl

4: 56 percent / 30percent aq. H₂O₂ / acetic acid / 48 h / 65 °C

5: 51 percent / ethanol

With hydrogenchloride; dihydrogen peroxide; sodium nitrite; In ethanol; acetic acid;
DOI:10.1021/ja00408a021

Reference yield:

: 87102-54-3
4-<(4-(dodecyloxy)phenyl)azo>phenol

: 78435-07-1
{4-[4-(4-Dodecyloxy-phenyl-ONN-azoxy)-phenoxy]-butyl}-trimethyl-ammonium; bromide

Guidance literature:: Multi-step reaction with 3 steps

2: 56 percent / 30percent aq. H₂O₂ / acetic acid / 48 h / 65 °C

3: 51 percent / ethanol

With dihydrogen peroxide; In ethanol; acetic acid;
DOI:10.1021/ja00408a021