1-(Methylamino)-4-((1-methylethyl)amino)anthraquinone

Base Information

Chemical Name:1-(Methylamino)-4-((1-methylethyl)amino)anthraquinone
CAS No.:15403-56-2
Molecular Formula:C18H18 N2 O2
Molecular Weight:294.353
Hs Code.:2922399090
European Community (EC) Number:239-420-6
DSSTox Substance ID:DTXSID00165522
Nikkaji Number:J218.419B
Wikidata:Q83034745

Synonyms:15403-56-2;Solvent Blue 102;1-(Methylamino)-4-((1-methylethyl)amino)anthraquinone;EINECS 239-420-6;1-(methylamino)-4-(propan-2-ylamino)anthracene-9,10-dione;1-(methylamino)-4-[(1-methylethyl)amino]anthraquinone;DTXSID00165522;1-(Methylamino)-4-[(1-methylethyl)amino]-9,10-anthracenedione;9,10-Anthracenedione, 1-(methylamino)-4-((1-methylethyl)amino)-

Suppliers and Price of 1-(Methylamino)-4-((1-methylethyl)amino)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

American Custom Chemicals Corporation
ERO BLUE 95.00%
5MG
$ 496.89

Total 12 raw suppliers

Chemical Property of 1-(Methylamino)-4-((1-methylethyl)amino)anthraquinone

Chemical Property:

Vapor Pressure:2.16E-11mmHg at 25°C
Melting Point:216-217 °C
Boiling Point:531.8°Cat760mmHg
PKA:6.56±0.20(Predicted)
Flash Point:200.5°C
PSA：114.36000
Density:1.272g/cm³
LogP:3.07870
XLogP3:4.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:294.136827821
Heavy Atom Count:22
Complexity:448

Purity/Quality:

98%Min ^*data from raw suppliers

ERO BLUE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)NC1=C2C(=C(C=C1)NC)C(=O)C3=CC=CC=C3C2=O

Technology Process of 1-(Methylamino)-4-((1-methylethyl)amino)anthraquinone

There total 1 articles about 1-(Methylamino)-4-((1-methylethyl)amino)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: