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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, 3-fluoro-4-methyl-

O=c1[nH]c2ccccc2c(c1F)C Request for Quotation
Chemical Name: 2(1H)-Quinolinone, 3-fluoro-4-methyl-
CAS Number: 198831-76-4
Product Number: AG002BR8(AGN-PC-0A7A8F)
Synonyms:
MDL No:
Molecular Formula: C10H8FNO
Molecular Weight: 177.1750

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Fluoro-4-methylquinolin-2(1H)-one is a versatile chemical compound with significant applications in organic synthesis. Its unique structure allows for various functional group manipulations, making it a valuable building block in the creation of complex molecules.One key application of 3-Fluoro-4-methylquinolin-2(1H)-one in chemical synthesis is its role as a precursor for the synthesis of pharmaceutical compounds. By converting this compound into other derivatives through substitution or addition reactions, chemists can access new molecules with potential therapeutic properties. Additionally, the presence of the fluoro group in the structure can impart specific properties to the final products, such as improved bioavailability or metabolic stability.Furthermore, 3-Fluoro-4-methylquinolin-2(1H)-one can serve as a valuable starting material for the preparation of functionalized heterocycles. By exploiting the reactivity of the fluorine atom and the quinoline ring system, chemists can introduce various substituents and functional groups to tailor the properties of the target molecules. This versatility opens up possibilities for the development of novel materials, agrochemicals, and dyes.In summary, the strategic use of 3-Fluoro-4-methylquinolin-2(1H)-one in chemical synthesis enables the efficient construction of diverse compounds with potential applications in pharmaceuticals, materials science, and agrochemicals.