2-[(4-benzoylbenzoyl)oxy]-N,N-dimethyl-N-[2-(tetradecanoyloxy)ethyl]ethanaminium bromide

Base Information

Chemical Name:2-[(4-benzoylbenzoyl)oxy]-N,N-dimethyl-N-[2-(tetradecanoyloxy)ethyl]ethanaminium bromide
CAS No.:108418-27-5
Molecular Formula:Br*C₃₄H₅₀NO₅
Molecular Weight:632.679
Hs Code.:

Synonyms:Ethanaminium,2-[(4-benzoylbenzoyl)oxy]-N,N-dimethyl-N-[2-[(1-oxotetradecyl)oxy]ethyl]-,bromide (9CI)

Suppliers and Price of 2-[(4-benzoylbenzoyl)oxy]-N,N-dimethyl-N-[2-(tetradecanoyloxy)ethyl]ethanaminium bromide

Supply Marketing:

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

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Chemical Property of 2-[(4-benzoylbenzoyl)oxy]-N,N-dimethyl-N-[2-(tetradecanoyloxy)ethyl]ethanaminium bromide

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:g/cm³

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2-[(4-benzoylbenzoyl)oxy]-N,N-dimethyl-N-[2-(tetradecanoyloxy)ethyl]ethanaminium bromide

There total 2 articles about 2-[(4-benzoylbenzoyl)oxy]-N,N-dimethyl-N-[2-(tetradecanoyloxy)ethyl]ethanaminium 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: 60.0%

: 43016-78-0
Myristinsaeure-2-(dimethylamino)ethylester

: 108418-20-8
4-Benzoylbenzoesaeure-2-bromethylester

: 108418-27-5
<2-(4-Benzoylbenzoyloxy)ethyl><2-(myristoyloxy)-ethyl>ammoniumbromid

Guidance literature:: In acetonitrile; 1 h, room temperature; 14 h, reflux;

Reference yield:

: 611-95-0
4-carboxybenzophenone

: 108418-27-5
<2-(4-Benzoylbenzoyloxy)ethyl><2-(myristoyloxy)-ethyl>ammoniumbromid

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / p-toluenesulfonic acid / toluene / 7.5 h

2: 60 percent / acetonitrile / 1 h, room temperature; 14 h, reflux

With toluene-4-sulfonic acid; In toluene; acetonitrile;