9,10-Anthracenedione, 1-(cyclohexylamino)-

Base Information

Chemical Name:9,10-Anthracenedione, 1-(cyclohexylamino)-
CAS No.:1096-48-6
Molecular Formula:C20H19NO2
Molecular Weight:305.376
Hs Code.:
European Community (EC) Number:214-143-3
DSSTox Substance ID:DTXSID2061484
Nikkaji Number:J52.239B
Wikidata:Q81989497
Mol file:1096-48-6.mol

Synonyms:1096-48-6;1-(cyclohexylamino)anthracene-9,10-dione;Solvent Red 168;71832-19-4;9,10-Anthracenedione, 1-(cyclohexylamino)-;9,10-Anthracenedione,1-(cyclohexylamino)-;1-cyclohexylaminoanthraquinone;1-(Cyclohexylaminoanthraquinone);EINECS 214-143-3;1-Cyclohexanaminoanthracene-9,10-dione;1-(Cyclohexylamino)anthraquinone;CBMicro_016349;cyclohexylamino-anthraquinone;SCHEMBL124201;1-cyclohexylamino anthraquinone;DTXSID2061484;CCG-5528;STK238278;AKOS000668397;SB83211;BIM-0016533.P001;AB00079558-01;ANTHRAQUINONE (9,10), 1-CYCLOHEXYLAMINO-;ANTHRAQUINONE (9,10), 1-(CYCLOHEXYLAMINO)-;F0123-0006

Suppliers and Price of 9,10-Anthracenedione, 1-(cyclohexylamino)-

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
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Total 14 raw suppliers

Chemical Property of 9,10-Anthracenedione, 1-(cyclohexylamino)-

Chemical Property:

Vapor Pressure:3.69E-11mmHg at 25°C
Refractive Index:1.663
Boiling Point:526.1 ºC at 760 mmHg
Flash Point:193.7 ºC
Density:1.266 g/cm³
XLogP3:5.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:305.141578849
Heavy Atom Count:23
Complexity:468

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(CC1)NC2=CC=CC3=C2C(=O)C4=CC=CC=C4C3=O
General Description 1-(Cyclohexylaminoanthraquinone) is a derivative of anthraquinone where a cyclohexylamino group is substituted at the 1-position. It can be synthesized through the direct amination of anthraquinone with cyclohexylamine, facilitated by rhodium(I) complexes, which selectively targets the α-position. 1-(cyclohexylaminoanthraquinone) shares structural similarities with N-alkylaminoanthraquinones, which have been studied for their supramolecular interactions with cyclodextrins, leading to the formation of fluorescent vesicles with applications in bioimaging and drug delivery. The cyclohexylamino substitution may similarly influence its photophysical and self-assembly properties, though specific data on this derivative were not detailed in the provided abstracts.

Technology Process of 9,10-Anthracenedione, 1-(cyclohexylamino)-

There total 9 articles about 9,10-Anthracenedione, 1-(cyclohexylamino)- 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: 97.0%