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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)-

2(1H)-Quinolinone

O=c1ccc2c([nH]1)cccc2 Request for Quotation
Chemical Name: 2(1H)-Quinolinone
CAS Number: 104534-80-7
Product Number: AG007XT1(AGN-PC-0JK7G3)
Synonyms:
MDL No:
Molecular Formula: C9H7NO
Molecular Weight: 145.1580

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Chemical Structure


Quinolinone is a versatile compound widely used in chemical synthesis due to its diverse range of applications. Its unique structure and reactivity make it a valuable building block in the production of various chemical products. In organic synthesis, Quinolinone serves as a key intermediate for the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. It can undergo various transformations, such as functional group modifications, cyclization reactions, and heterocyclic ring formations, making it a powerful tool for creating complex molecular structures. Additionally, Quinolinone derivatives exhibit promising biological activities, making them attractive candidates for drug discovery and development. The ability of Quinolinone to participate in multiple types of chemical reactions and its potential for yielding structurally diverse compounds make it a valuable resource in the field of chemical synthesis.