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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, 1,8-dichloro-

Clc1cccc2c1C(=O)c1c(C2=O)cccc1Cl Request for Quotation
Chemical Name: 9,10-Anthracenedione, 1,8-dichloro-
CAS Number: 82-43-9
Product Number: AG003B0T(AGN-PC-0JK7PN)
Synonyms:
MDL No:
Molecular Formula: C14H6Cl2O2
Molecular Weight: 277.1022

Identification/Properties

Properties
MP:
201.5-203 °C(lit.)
BP:
455.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.4730 (estimate)
Computed Properties
Molecular Weight:
277.1g/mol
XLogP3:
4.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
275.974g/mol
Monoisotopic Mass:
275.974g/mol
Topological Polar Surface Area:
34.1A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
350
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


1,8-Dichloroanthracene-9,10-dione is a versatile compound commonly utilized in chemical synthesis as a key intermediate in the production of various organic molecules and materials. With its unique chemical structure, this compound serves as a valuable building block for the creation of complex organic compounds and functional materials in the field of organic synthesis. Its presence in numerous synthetic pathways enables chemists to access a wide range of compounds with diverse properties and applications. In reactions involving 1,8-Dichloroanthracene-9,10-dione, its chlorinated aromatic core and reactive carbonyl groups play crucial roles in facilitating desired transformations and forming important chemical bonds. These transformations may include functional group interconversions, cyclization reactions, and the introduction of additional substituents to modulate chemical and physical properties.Moreover, the unique reactivity and structural features of 1,8-Dichloroanthracene-9,10-dione make it a valuable tool in the preparation of compounds with potential applications in pharmaceuticals, agrochemicals, and materials science. By leveraging the versatility of this compound in chemical synthesis, researchers can access novel molecules with tailored properties for various industrial and academic applications.