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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)-

Quinoline-4,7-diol

Oc1ccc2c(c1)[nH]ccc2=O Request for Quotation
Chemical Name: Quinoline-4,7-diol
CAS Number: 955938-89-3
Product Number: AG005ZPN(AGN-PC-0WAHRK)
Synonyms:
MDL No:
Molecular Formula: C9H7NO2
Molecular Weight: 161.1574

Identification/Properties

Properties
BP:
397.2±22.0°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
161.16g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
161.048g/mol
Monoisotopic Mass:
161.048g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
225
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Hydroxyquinolin-4(1H)-one, also known as 7-Hydroxy-4-quinolinol, is a versatile compound widely used in chemical synthesis processes. This organic molecule has found various applications in the field of chemistry due to its unique structure and reactivity.One of the key applications of 7-Hydroxyquinolin-4(1H)-one in chemical synthesis is as a building block for the synthesis of heterocyclic compounds. Its hydroxyquinoline scaffold provides a valuable starting point for the construction of complex molecules with diverse functionalities. By utilizing the reactive hydroxyl group and the quinoline ring system, chemists can introduce different substituents and functional groups to tailor the properties of the final product.Moreover, 7-Hydroxyquinolin-4(1H)-one serves as a key intermediate in the synthesis of pharmaceutical compounds. The presence of the quinoline moiety in its structure makes it a valuable precursor for developing bioactive molecules with potential therapeutic applications. Chemists can modify the 7-Hydroxyquinolin-4(1H)-one molecule through various reactions to introduce specific pharmacophores or enhance biological activities.In addition, this compound has been employed in the preparation of coordination complexes and chelating agents. Its ability to form stable complexes with metal ions makes it useful in metal coordination chemistry and catalysis. By chelating with metal ions, 7-Hydroxyquinolin-4(1H)-one can exhibit enhanced properties or serve as a catalyst in various chemical transformations.Overall, the versatile nature of 7-Hydroxyquinolin-4(1H)-one makes it a valuable resource in chemical synthesis, enabling the creation of diverse compounds with significant applications in medicinal chemistry, materials science, and catalysis.