N-<4-<10-<(2-Hydroxyethyl)dimethylammonio>decyloxy>salicylidene>-4-(octyloxy)aniline bromide

Base Information

Chemical Name:N-<4-<10-<(2-Hydroxyethyl)dimethylammonio>decyloxy>salicylidene>-4-(octyloxy)aniline bromide
CAS No.:126046-35-3
Molecular Formula:Br*C₃₅H₅₇N₂O₄
Molecular Weight:649.753
Hs Code.:

Synonyms:N-<4-<10-<(2-Hydroxyethyl)dimethylammonio>decyloxy>salicylidene>-4-(octyloxy)aniline bromide

Suppliers and Price of N-<4-<10-<(2-Hydroxyethyl)dimethylammonio>decyloxy>salicylidene>-4-(octyloxy)aniline 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-<4-<10-<(2-Hydroxyethyl)dimethylammonio>decyloxy>salicylidene>-4-(octyloxy)aniline bromide

Chemical Property:

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Technology Process of N-<4-<10-<(2-Hydroxyethyl)dimethylammonio>decyloxy>salicylidene>-4-(octyloxy)aniline bromide

There total 6 articles about N-<4-<10-<(2-Hydroxyethyl)dimethylammonio>decyloxy>salicylidene>-4-(octyloxy)aniline 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:

: 39905-45-8
4-octyloxyaniline

: 126046-35-3
N-<4-<10-<(2-Hydroxyethyl)dimethylammonio>decyloxy>salicylidene>-4-(octyloxy)aniline bromide

Guidance literature:: Multi-step reaction with 2 steps

1: ethanol / Ambient temperature

2: benzene / Heating

In ethanol; benzene;
DOI:10.1002/recl.19941130407

Reference yield:

: 108-01-0
2-(N,N-dimethylamino)ethanol

: 39905-45-8
4-octyloxyaniline

: 176519-99-6
4-(10-Bromo-decyloxy)-2-hydroxy-benzaldehyde

: 126046-35-3
N-<4-<10-<(2-Hydroxyethyl)dimethylammonio>decyloxy>salicylidene>-4-(octyloxy)aniline bromide

Guidance literature:: Multistep reaction;

Reference yield:

: 4101-68-2
1,10-dibromodecane

: 126046-35-3
N-<4-<10-<(2-Hydroxyethyl)dimethylammonio>decyloxy>salicylidene>-4-(octyloxy)aniline bromide

Guidance literature:: Multi-step reaction with 3 steps

1: KOH / ethanol / Heating

2: ethanol / Ambient temperature

3: benzene / Heating

With potassium hydroxide; In ethanol; benzene;
DOI:10.1002/recl.19941130407