3-<(3-Benzylamino-4-oxo-1-naphthyliden)amino>-4-hydroxy-1-naphthalinsulfonsaeure

Base Information

Chemical Name:3-<(3-Benzylamino-4-oxo-1-naphthyliden)amino>-4-hydroxy-1-naphthalinsulfonsaeure
CAS No.:87459-38-9
Molecular Formula:C₂₇H₂₀N₂O₅S
Molecular Weight:484.532
Hs Code.:

Synonyms:3-<(3-Benzylamino-4-oxo-1-naphthyliden)amino>-4-hydroxy-1-naphthalinsulfonsaeure

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Chemical Property of 3-<(3-Benzylamino-4-oxo-1-naphthyliden)amino>-4-hydroxy-1-naphthalinsulfonsaeure

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Technology Process of 3-<(3-Benzylamino-4-oxo-1-naphthyliden)amino>-4-hydroxy-1-naphthalinsulfonsaeure

There total 4 articles about 3-<(3-Benzylamino-4-oxo-1-naphthyliden)amino>-4-hydroxy-1-naphthalinsulfonsaeure 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: 70.0%

: 567-13-5
2-amino-1-naphthol-4-sulfonic acid

: 90908-05-7
N-Benzyl-N-(4-methoxy-1(2H)-oxo-2-naphthyliden)ammoniumfluorsulfonat

: 87459-38-9
3-<(3-Benzylamino-4-oxo-1-naphthyliden)amino>-4-hydroxy-1-naphthalinsulfonsaeure

Guidance literature:: With pyridine; In 1,2-dimethoxyethane; Ambient temperature;
DOI:10.1002/ardp.19843170407

Reference yield:

: 24137-17-5
2-benzylamino-[1,4]naphthoquinone

: 87459-38-9
3-<(3-Benzylamino-4-oxo-1-naphthyliden)amino>-4-hydroxy-1-naphthalinsulfonsaeure

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / 1,2-dimethoxy-ethane / Heating

2: 70 percent / pyridine / 1,2-dimethoxy-ethane / Ambient temperature

With pyridine; In 1,2-dimethoxyethane;
DOI:10.1002/ardp.19843170407

Reference yield:

: 100-46-9
benzylamine

: 87459-38-9
3-<(3-Benzylamino-4-oxo-1-naphthyliden)amino>-4-hydroxy-1-naphthalinsulfonsaeure

Guidance literature:: Multi-step reaction with 3 steps

1: 43 percent / aq. ethanol / Ambient temperature

2: 73 percent / 1,2-dimethoxy-ethane / Heating

3: 70 percent / pyridine / 1,2-dimethoxy-ethane / Ambient temperature

With pyridine; In 1,2-dimethoxyethane; ethanol;
DOI:10.1002/ardp.19843170407