N-n-Cetyl-N,N-dimethyl-N-ammonium Bromide

Base Information

Chemical Name:N-n-Cetyl-N,N-dimethyl-N-ammonium Bromide
CAS No.:77552-04-6
Molecular Formula:Br*C₃₂H₅₀NOS
Molecular Weight:576.725
Hs Code.:

N-n-Cetyl-N,N-dimethyl-N-<p-(benzylthio)benzyl>ammonium Bromide

Synonyms:N-n-Cetyl-N,N-dimethyl-N-ammonium Bromide

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

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Chemical Property of N-n-Cetyl-N,N-dimethyl-N-ammonium Bromide

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Technology Process of N-n-Cetyl-N,N-dimethyl-N-ammonium Bromide

There total 4 articles about N-n-Cetyl-N,N-dimethyl-N-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: 66.0%

: 112-69-6
N,N-dimethylhexadecylamine

: 77552-03-5
S-[4-(bromomethyl)phenyl] benzenecarbothioc acid

: 77552-04-6
N-n-Cetyl-N,N-dimethyl-N-ammonium Bromide

Guidance literature:: In nitromethane; for 16h;
DOI:10.1021/jo00328a008

Reference yield:

: 10371-42-3
S-(4-methylphenyl) thiobenzoate

: 77552-04-6
N-n-Cetyl-N,N-dimethyl-N-ammonium Bromide

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / N-bromosuccinimide / CCl₄ / 1.5 h / Heating; Irradiation

2: 66 percent / nitromethane / 16 h

With N-Bromosuccinimide; In tetrachloromethane; nitromethane;
DOI:10.1021/jo00328a008

Reference yield:

: 98-88-4
benzoyl chloride

: 77552-04-6
N-n-Cetyl-N,N-dimethyl-N-ammonium Bromide

Guidance literature:: Multi-step reaction with 3 steps

1: 64 percent / triethylamine / diethyl ether / 2 h / ice/water bath

2: 71 percent / N-bromosuccinimide / CCl₄ / 1.5 h / Heating; Irradiation

3: 66 percent / nitromethane / 16 h

With N-Bromosuccinimide; triethylamine; In tetrachloromethane; diethyl ether; nitromethane;
DOI:10.1021/jo00328a008