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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-fluoroquinoline-4-carboxylic acid

Fc1ccc2c(c1)c(ccn2)C(=O)O Request for Quotation
Chemical Name: 6-fluoroquinoline-4-carboxylic acid
CAS Number: 220844-73-5
Product Number: AG00BI71(AGN-PC-01WKEY)
Synonyms:
MDL No:
Molecular Formula: C10H6FNO2
Molecular Weight: 191.1585

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Chemical Structure


6-Fluoro-4-quinolinecarboxylic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique chemical properties. In chemical synthesis, $name$ serves as a key building block for the synthesis of complex molecules through various reactions such as esterification, amidation, and halogenation. Its fluorine substituent enhances the compound's reactivity and can be selectively manipulated to introduce specific functional groups into target molecules. This enables chemists to design and synthesize novel compounds with tailored properties and activities for a wide range of applications. Additionally, the quinoline ring structure of $name$ provides an aromatic scaffold that can participate in diverse aromatic substitution reactions, further expanding its utility in chemical synthesis processes.