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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)-

4-Quinolinol, 2-phenyl-

Oc1cc(nc2c1cccc2)c1ccccc1 Request for Quotation
Chemical Name: 4-Quinolinol, 2-phenyl-
CAS Number: 1144-20-3
Product Number: AG000B8R(AGN-PC-0NYGJF)
Synonyms:
MDL No:
Molecular Formula: C15H11NO
Molecular Weight: 221.2539

Identification/Properties

Computed Properties
Molecular Weight:
221.259g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
221.084g/mol
Monoisotopic Mass:
221.084g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
328
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Phenylquinolin-4-ol, commonly referred to as $name$, is a versatile compound that finds extensive application in chemical synthesis processes. With its unique structure and reactivity, this compound is a valuable building block in the creation of various organic molecules and materials. One of the key applications of 2-Phenylquinolin-4-ol in chemical synthesis is its role as a key intermediate in the production of pharmaceutical compounds. Its ability to undergo various functionalization reactions makes it an essential component in the synthesis of drug candidates and active pharmaceutical ingredients. Additionally, 2-Phenylquinolin-4-ol serves as a crucial starting material in the development of novel organic dyes and fluorescent materials. Its aromatic backbone and functional groups make it a versatile precursor for the creation of vibrant and light-responsive molecules. In summary, the significance of 2-Phenylquinolin-4-ol in chemical synthesis lies in its ability to serve as a fundamental building block for the generation of diverse organic compounds with valuable applications in pharmaceuticals, materials science, and beyond.