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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)-

8-Quinolinol, sulfate (2:1) (salt)

OS(=O)(=O)O.Oc1cccc2c1nccc2.Oc1cccc2c1nccc2 Request for Quotation
Chemical Name: 8-Quinolinol, sulfate (2:1) (salt)
CAS Number: 134-31-6
Product Number: AG0037UA(AGN-PC-0PK8CA)
Synonyms:
MDL No:
Molecular Formula: C18H16N2O6S
Molecular Weight: 388.3944

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Chemical Structure


8-Hydroxyquinoline sulfate is widely utilized in chemical synthesis as a versatile reagent due to its unique properties. This compound serves as a chelating agent, forming stable complexes with various metal ions, particularly transition metals like copper, nickel, and cobalt. These metal complexes play a crucial role in catalyzing a range of organic reactions, including oxidation, reduction, and carbon-carbon bond formation.In addition to its chelating capabilities, 8-Hydroxyquinoline sulfate also demonstrates antimicrobial activity, making it a valuable component in the formulation of disinfectants and antimicrobial agents. Its ability to selectively bind to certain metal ions can also be harnessed in analytical chemistry applications for metal ion detection and quantification.Overall, the diverse applications of 8-Hydroxyquinoline sulfate in chemical synthesis make it a valuable tool for researchers and chemists working in various fields, including coordination chemistry, organic synthesis, and materials science.