9,10-Anthracenedione, 5-amino-1,4-dichloro-

Base Information

Chemical Name:9,10-Anthracenedione, 5-amino-1,4-dichloro-
CAS No.:3223-94-7
Molecular Formula:C14H7 Cl2 N O2
Molecular Weight:292.121
Hs Code.:2922399090
European Community (EC) Number:221-751-2
UNII:8PVZ2WD2GK
DSSTox Substance ID:DTXSID1062914
Nikkaji Number:J262.330G
Wikidata:Q81990356
Mol file:3223-94-7.mol

Synonyms:3223-94-7;Anthraquinone, 5-amino-1,4-dichloro-;9,10-Anthracenedione, 5-amino-1,4-dichloro-;5-Amino-1,4-dichloroanthraquinone;5-amino-1,4-dichloroanthracene-9,10-dione;EINECS 221-751-2;5-Amino-1,4-dichloro-9,10-anthracenedione;1-amino-5,8-dichloroanthraquinone;8PVZ2WD2GK;SCHEMBL8777793;DTXSID1062914;1,4-Dichloro-5-aminoanthraquinone

Suppliers and Price of 9,10-Anthracenedione, 5-amino-1,4-dichloro-

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

American Custom Chemicals Corporation
9,10-ANTHRACENEDIONE,5-AMINO-1,4-DICHLORO- 95.00%
5MG
$ 497.28

Total 6 raw suppliers

Chemical Property of 9,10-Anthracenedione, 5-amino-1,4-dichloro-

Chemical Property:

Vapor Pressure:3.13E-11mmHg at 25°C
Melting Point:199 °C
Boiling Point:527.9°Cat760mmHg
PKA:-1.91±0.20(Predicted)
Flash Point:273.1°C
PSA：60.16000
Density:1.576g/cm³
LogP:3.93220
XLogP3:4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:290.9853839
Heavy Atom Count:19
Complexity:414

Purity/Quality:

99% ^*data from raw suppliers

9,10-ANTHRACENEDIONE,5-AMINO-1,4-DICHLORO- 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C(C(=C1)N)C(=O)C3=C(C=CC(=C3C2=O)Cl)Cl

Technology Process of 9,10-Anthracenedione, 5-amino-1,4-dichloro-

There total 6 articles about 9,10-Anthracenedione, 5-amino-1,4-dichloro- 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%

: 3223-90-3
1,4-dichloro-5-nitro-anthraquinone

: 3223-94-7
1-amino-5,8-dichloroanthraquinone

Guidance literature:: With iron; acetic acid;
DOI:10.1016/S0040-4039(00)73069-3

Reference yield:

: 602-25-5
1,4-dichloroanthraquinone

: 3223-94-7
1-amino-5,8-dichloroanthraquinone

Guidance literature:: Multi-step reaction with 2 steps

1: 67 percent / HNO₃, H₂SO₄

2: 70 percent / Fe/AcOH

With sulfuric acid; nitric acid; iron; acetic acid;
DOI:10.1016/S0040-4039(00)73069-3

Reference yield:

: leucoquinazirin

: 3223-94-7
1-amino-5,8-dichloroanthraquinone

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) PCl₅ / 2.) pentanol, reflux

2: 67 percent / HNO₃, H₂SO₄

3: 70 percent / Fe/AcOH

With phosphorus pentachloride; sulfuric acid; nitric acid; iron; acetic acid;
DOI:10.1016/S0040-4039(00)73069-3