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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-(pyridin-2-ylamino)quinolin-8-ol

Oc1cccc2c1nc(cc2)Nc1ccccn1 Request for Quotation
Chemical Name: 2-(pyridin-2-ylamino)quinolin-8-ol
CAS Number: 70125-23-4
Product Number: AG005XK3(AGN-PC-0K4HRA)
Synonyms:
MDL No:
Molecular Formula: C14H11N3O
Molecular Weight: 237.2566

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
237.262g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
237.09g/mol
Monoisotopic Mass:
237.09g/mol
Topological Polar Surface Area:
58A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
274
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-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Pyridin-2-ylamino)quinolin-8-ol is a versatile compound widely employed in chemical synthesis for its unique properties and diverse applications. This compound is commonly utilized as a key building block in the synthesis of various organic molecules and pharmaceutical intermediates. Its structure, characterized by the presence of a quinoline ring combined with a pyridine moiety, confers distinctive reactivity that enables it to participate in a range of synthetic transformations.One of the prominent applications of 2-(Pyridin-2-ylamino)quinolin-8-ol is in the construction of heterocyclic compounds, where its presence as a functional group facilitates the formation of complex ring systems. The compound's ability to undergo selective functionalization at both the quinoline and pyridine positions allows for precise modification of the molecular structure, making it a valuable tool in the design of novel chemical entities. Additionally, the nitrogen atoms present in the pyridine and quinoline rings can serve as points for further derivatization, enabling the creation of diverse chemical libraries for drug discovery and material science.Moreover, 2-(Pyridin-2-ylamino)quinolin-8-ol has found utility in the synthesis of fluorescent probes and molecular sensors due to its inherent fluorescence properties. By incorporating this compound into the structure of fluorescent dyes or sensors, researchers can develop molecular tools for detecting specific analytes or monitoring biological processes with high sensitivity and selectivity. The tunable emission characteristics of 2-(Pyridin-2-ylamino)quinolin-8-ol make it a valuable component in the design of molecular probes for various imaging and detection applications.Overall, the versatile nature of 2-(Pyridin-2-ylamino)quinolin-8-ol makes it a valuable asset in chemical synthesis, offering researchers a versatile platform for the construction of complex molecules, heterocyclic scaffolds, and functional materials with diverse applications in medicinal chemistry, materials science, and chemical biology.