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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)-

5-Fluoroquinolin-6-ol

Oc1ccc2c(c1F)cccn2 Request for Quotation
Chemical Name: 5-Fluoroquinolin-6-ol
CAS Number: 1261470-32-9
Product Number: AG000RS6(AGN-PC-0WAG9Z)
Synonyms:
MDL No:
Molecular Formula: C9H6FNO
Molecular Weight: 163.1484

Identification/Properties

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Fluoroquinolin-6-ol is a versatile chemical compound that finds widespread application in chemical synthesis. Thanks to its unique structure and properties, this compound serves as a valuable building block in the creation of various advanced materials and pharmaceuticals. In chemical synthesis, 5-Fluoroquinolin-6-ol is utilized as a key intermediate in the production of pharmaceutical drugs, agrochemicals, and fine chemicals. Its functional groups and reactivity make it a highly sought-after reagent for the formation of new molecular structures through diverse chemical transformations including functional group modifications, cyclization reactions, and heterocyclic synthesis. Additionally, the presence of the fluorine atom in the molecule enhances the compound's bioactivity and allows for the development of novel drug candidates with improved pharmacological profiles. This compound's significance in chemical synthesis lies in its ability to participate in various synthetic pathways to produce complex molecules with enhanced properties and functionalities.