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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)-

1,4-Chrysenedione

O=C1C=CC(=O)c2c1ccc1c2ccc2c1cccc2 Request for Quotation
Chemical Name: 1,4-Chrysenedione
CAS Number: 100900-16-1
Product Number: AG00035I(AGN-PC-0JNG6K)
Synonyms:
MDL No:
Molecular Formula: C18H10O2
Molecular Weight: 258.2708

Identification/Properties

Properties
MP:
>212°C (dec.)
Storage:
2-8℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
258.276g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
258.068g/mol
Monoisotopic Mass:
258.068g/mol
Topological Polar Surface Area:
34.1A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
464
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,4-Chrysenequinone is a versatile compound often employed in chemical synthesis due to its capability to undergo a variety of reactions, making it a valuable building block in organic chemistry. This compound can participate in cycloaddition reactions with dienes or enol ethers to form complex polycyclic aromatic hydrocarbons, which are important intermediates in the synthesis of pharmaceuticals, agrochemicals, and materials science. Additionally, 1,4-Chrysenequinone can be utilized in the production of dyes and pigments, as well as in the development of organic electronic materials. Its unique structure and reactivity make it a valuable tool for chemists seeking to design and create a diverse range of compounds for various applications in the field of chemistry.