2-amino-1,4-naphthalenedione

Base Information

Chemical Name:2-amino-1,4-naphthalenedione
CAS No.:175886-03-0
Molecular Formula:C₁₈H₁₃NO₄
Molecular Weight:307.306
Hs Code.:

2-<N-(4-acetoxyphenyl)>amino-1,4-naphthalenedione

Synonyms:

Suppliers and Price of 2-amino-1,4-naphthalenedione

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-amino-1,4-naphthalenedione

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-amino-1,4-naphthalenedione

There total 3 articles about 2-amino-1,4-naphthalenedione 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: 64.0%

: 52200-97-2
2-<(4-Hydroxyphenyl)amino>-1,4-naphthochinon

: 108-24-7
acetic anhydride

: 175886-03-0
2-amino-1,4-naphthalenedione

Guidance literature:: With sulfuric acid; Ambient temperature;
DOI:10.1002/jhet.5570330120

Reference yield:

: 123-30-8
4-amino-phenol

: 175886-03-0
2-amino-1,4-naphthalenedione

Guidance literature:: Multi-step reaction with 2 steps

1: 59 percent / ethanol / Ambient temperature

2: 64 percent / H₂SO₄ / Ambient temperature

With sulfuric acid; In ethanol;
DOI:10.1002/jhet.5570330120

Reference yield:

: 130-15-4
[1,4]naphthoquinone

: 175886-03-0
2-amino-1,4-naphthalenedione

Guidance literature:: Multi-step reaction with 2 steps

1: 59 percent / ethanol / Ambient temperature

2: 64 percent / H₂SO₄ / Ambient temperature

With sulfuric acid; In ethanol;
DOI:10.1002/jhet.5570330120