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  2. 9,10-Anthracenedione, 1,4-bis[[2-(4-hydroxyphenyl)ethyl]amino]-

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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

9,10-Anthracenedione, 1,4-bis[[2-(4-hydroxyphenyl)ethyl]amino]-

O=C1c2c(NCCc3ccc(cc3)O)ccc(c2C(=O)c2c1cccc2)NCCc1ccc(cc1)O Request for Quotation
Chemical Name: 9,10-Anthracenedione, 1,4-bis[[2-(4-hydroxyphenyl)ethyl]amino]-
CAS Number: 96969-83-4
Product Number: AG005SGM(AGN-PC-0KLMMX)
Synonyms:
MDL No: MFCD00208443
Molecular Formula: C30H26N2O4
Molecular Weight: 478.5384

Identification/Properties

Properties
BP:
780.2±60.0 °C(Predicted)
Form:
Solid
Solubility:
DMSO: ≥10mg/mL
Computed Properties
Molecular Weight:
478.548g/mol
XLogP3:
7.1
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
8
Exact Mass:
478.189g/mol
Monoisotopic Mass:
478.189g/mol
Topological Polar Surface Area:
98.7A^2
Heavy Atom Count:
36
Formal Charge:
0
Complexity:
681
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,4-bis[(p-hydroxyphenethyl)amino]-anthraquinone, also known as $name$, is a versatile compound widely utilized in chemical synthesis. Its primary application lies in its role as a potent catalyst in various synthetic reactions, particularly in organic chemistry. This compound exhibits remarkable catalytic activity in a range of transformations, including but not limited to, C-C bond formation, oxidation reactions, and complex molecule synthesis. Its unique structure provides a stable platform for promoting desired chemical reactions while maintaining high selectivity and efficiency. Chemists often rely on $name$ to facilitate the synthesis of intricate molecular structures with precision and control, making it an indispensable tool in modern synthetic chemistry.