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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(1H)-Quinolinone, 4-hydroxy-3-methyl-

O=c1[nH]c2ccccc2c(c1C)O Request for Quotation
Chemical Name: 2(1H)-Quinolinone, 4-hydroxy-3-methyl-
CAS Number: 1873-59-2
Product Number: AG00AMTF(AGN-PC-0AAGFM)
Synonyms:
MDL No:
Molecular Formula: C10H9NO2
Molecular Weight: 175.1840

Identification/Properties

Computed Properties
Molecular Weight:
175.187g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
175.063g/mol
Monoisotopic Mass:
175.063g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
270
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


4-Hydroxy-3-methylquinolin-2(1H)-one, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This molecule plays a crucial role in organic chemistry as a key building block for the synthesis of various complex organic compounds. Its specific structure and reactivity make it a valuable intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, $name$ serves as a precursor for the preparation of heterocyclic compounds, which are essential in drug discovery and development. By undergoing various chemical reactions such as substitution, addition, and rearrangement, $name$ can be transformed into a wide range of derivatives with diverse functional groups. These derivatives exhibit different properties and biological activities, making them valuable tools for the design and synthesis of new molecules with specific applications.Furthermore, the presence of the hydroxyl and methyl groups on the quinoline ring of $name$ provides additional sites for modifications, allowing chemists to fine-tune the properties of the resulting compounds. This flexibility in structural modification makes 4-Hydroxy-3-methylquinolin-2(1H)-one a highly versatile intermediate in chemical synthesis, enabling the construction of complex molecules with tailored characteristics for various industrial and research applications.