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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, 1,1'-iminobis-

O=C1c2c(cccc2C(=O)c2c1cccc2)Nc1cccc2c1C(=O)c1ccccc1C2=O Request for Quotation
Chemical Name: 9,10-Anthracenedione, 1,1'-iminobis-
CAS Number: 82-22-4
Product Number: AG003D82(AGN-PC-0JK7PG)
Synonyms:
MDL No:
Molecular Formula: C28H15NO4
Molecular Weight: 429.423

Identification/Properties

Properties
MP:
300℃
Form:
Solid
Computed Properties
Molecular Weight:
429.431g/mol
XLogP3:
5.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
429.1g/mol
Monoisotopic Mass:
429.1g/mol
Topological Polar Surface Area:
80.3A^2
Heavy Atom Count:
33
Formal Charge:
0
Complexity:
783
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H320
Precautionary Statements:
P264-P337+P313-P305+P351+P338-P332+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,1'-Azanediylbis(anthracene-9,10-dione) is a versatile and potent compound commonly used in chemical synthesis as a powerful oxidizing agent. This compound plays a crucial role in various synthetic processes, particularly in the oxidation of organic substrates.In chemical synthesis, 1,1'-Azanediylbis(anthracene-9,10-dione) is frequently utilized to facilitate the conversion of alcohols to carbonyl compounds through selective oxidation reactions. Its high reactivity and selectivity make it an essential tool for the controlled oxidation of a wide range of organic molecules.Additionally, this compound is employed in the synthesis of various functionalized organic molecules and complex natural products due to its ability to induce specific and efficient oxidative transformations. Its unique properties make it a valuable reagent in the development of novel synthetic methodologies and the preparation of structurally diverse compounds.Overall, 1,1'-Azanediylbis(anthracene-9,10-dione) serves as a key component in chemical synthesis, enabling chemists to access new and diverse compounds with enhanced efficiency and selectivity.