Ethyl-2-(2-amino-3,6-dimethoxyphenyl)-azo-2-cyanoacetat

Base Information

Chemical Name:Ethyl-2-(2-amino-3,6-dimethoxyphenyl)-azo-2-cyanoacetat
CAS No.:26002-60-8
Molecular Formula:C₁₃H₁₆N₄O₄
Molecular Weight:292.294
Hs Code.:

Synonyms:

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Chemical Property of Ethyl-2-(2-amino-3,6-dimethoxyphenyl)-azo-2-cyanoacetat

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Technology Process of Ethyl-2-(2-amino-3,6-dimethoxyphenyl)-azo-2-cyanoacetat

There total 7 articles about Ethyl-2-(2-amino-3,6-dimethoxyphenyl)-azo-2-cyanoacetat 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:

: 26002-59-5
Ethyl-2-cyano-2-(3,6-dimethoxy-2-nitrophenyl)-azoacetat

: 26002-60-8
Ethyl-2-(2-amino-3,6-dimethoxyphenyl)-azo-2-cyanoacetat

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethyl acetate;
DOI:10.1039/j39700000583

Reference yield:

: 2785-98-0
2,5-dimethoxybenzoic acid

: 26002-60-8
Ethyl-2-(2-amino-3,6-dimethoxyphenyl)-azo-2-cyanoacetat

Guidance literature:: Multi-step reaction with 6 steps

1: H₂SO₄

2: aq. NH₃

3: HNO₃

4: aq. Br₂, aq. NaOH

5: (i) aq. NaNO₂, aq. HCl, (ii) /BRN= 605871/, NaOAc

6: H₂ / Pd-C / ethyl acetate

With ammonium hydroxide; sodium hydroxide; sulfuric acid; hydrogen; bromine; nitric acid; palladium on activated charcoal; In ethyl acetate;
DOI:10.1039/j39700000583

Reference yield:

: 26002-57-3
2-amino-3-nitrohydroquinone dimethylether

: 26002-60-8
Ethyl-2-(2-amino-3,6-dimethoxyphenyl)-azo-2-cyanoacetat

Guidance literature:: Multi-step reaction with 2 steps

1: (i) aq. NaNO₂, aq. HCl, (ii) /BRN= 605871/, NaOAc

2: H₂ / Pd-C / ethyl acetate

With hydrogen; palladium on activated charcoal; In ethyl acetate;
DOI:10.1039/j39700000583