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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)-

6-Anilino-5,8-quinolinedione

O=C1C=C(Nc2ccccc2)C(=O)c2c1nccc2 Request for Quotation
Chemical Name: 6-Anilino-5,8-quinolinedione
CAS Number: 91300-60-6
Product Number: AG006OUJ(AGN-PC-0WAG2F)
Synonyms:
MDL No:
Molecular Formula: C15H10N2O2
Molecular Weight: 250.2521

Identification/Properties

Computed Properties
Molecular Weight:
250.257g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
250.074g/mol
Monoisotopic Mass:
250.074g/mol
Topological Polar Surface Area:
59.1A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
410
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


6-(Phenylamino)quinoline-5,8-dione, also known as $name$, serves as a versatile building block in chemical synthesis due to its unique structural properties and reactivity. It can be utilized in various synthetic pathways to create structurally diverse compounds with potential applications in pharmaceuticals, materials science, and agrochemicals. In chemical synthesis, $name$ is commonly employed as a key intermediate to introduce the quinoline moiety into the molecular structure, enabling the formation of novel compounds with enhanced biological or physical properties. Specifically, $name$ can participate in diverse organic reactions such as nucleophilic substitution, oxidative coupling, and heterocyclic ring formation, offering chemists a valuable tool for the rapid generation of complex molecules with tailored functionalities. Its strategic placement of the phenylamino group and quinone core facilitates the construction of intricate chemical frameworks, making it a valuable asset in the synthesis of biologically active compounds and advanced materials.