Red Violet 2RN Acid Anthraquinone

Base Information

Chemical Name:Red Violet 2RN Acid Anthraquinone
CAS No.:81-79-8
Molecular Formula:C21H13NO4
Molecular Weight:343.339
Hs Code.:
NSC Number:7578
DSSTox Substance ID:DTXSID10278475
Wikidata:Q82010374
ChEMBL ID:CHEMBL1373390

Synonyms:Red Violet 2RN Acid Anthraquinone;MLS000737881;81-79-8;NSC7578;1-Anilino-9,10-dioxo-2-anthroic acid;1-anilino-9,10-dioxoanthracene-2-carboxylic acid;CHEMBL1373390;DTXSID10278475;CHEBI:167991;NSC-7578;SMR000528072;1-anilino-9,10-dioxo-9,10-dihydro-2-anthracenecarboxylic acid;1-anilino-9,10-dioxo-9,10-dihydroanthracene-2-carboxylic acid;2-Anthracenecarboxylic acid,10-dihydro-9,10-dioxo-1-(phenylamino)-

Suppliers and Price of Red Violet 2RN Acid Anthraquinone

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 7 raw suppliers

Chemical Property of Red Violet 2RN Acid Anthraquinone

Chemical Property:

Vapor Pressure:2.01E-14mmHg at 25°C
Boiling Point:582.8°Cat760mmHg
Flash Point:306.3°C
Density:1.444g/cm³
XLogP3:4.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:343.08445790
Heavy Atom Count:26
Complexity:583

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)NC2=C(C=CC3=C2C(=O)C4=CC=CC=C4C3=O)C(=O)O

Technology Process of Red Violet 2RN Acid Anthraquinone

There total 7 articles about Red Violet 2RN Acid Anthraquinone 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:

: 84-54-8
2-methylanthracene-9,10-dione

: 81-79-8
1-anilino-9,10-dioxo-9,10-dihydro-anthracene-2-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1: nitrobenzene; iodine; sulfuryl chloride

2: nitrobenzene; bromine / 160 - 170 °C

4: sodium bi chromate; glacial acetic acid

5: potassium acetate; copper acetate

With sulfuryl dichloride; sodium dichromate; bromine; iodine; potassium acetate; copper (I) acetate; acetic acid; nitrobenzene;

Reference yield:

: 82-23-5
1-chloro-9,10-dioxo-9,10-dihydro-anthracene-2-carboxylic acid

: 62-53-3
aniline

: 81-79-8
1-anilino-9,10-dioxo-9,10-dihydro-anthracene-2-carboxylic acid

Guidance literature:: With potassium acetate; copper (I) acetate;

Reference yield:

: 129-35-1
1-chloro-2-methylanthraquinone

: 81-79-8
1-anilino-9,10-dioxo-9,10-dihydro-anthracene-2-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: nitrobenzene; bromine / 160 - 170 °C

3: sodium bi chromate; glacial acetic acid

4: potassium acetate; copper acetate

With sodium dichromate; bromine; potassium acetate; copper (I) acetate; acetic acid; nitrobenzene;