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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, 5-bromo-

O=c1ccc2c([nH]1)cccc2Br Request for Quotation
Chemical Name: 2(1H)-Quinolinone, 5-bromo-
CAS Number: 99465-09-5
Product Number: AG005SB8(AGN-PC-000R2C)
Synonyms:
MDL No: MFCD11557206
Molecular Formula: C9H6BrNO
Molecular Weight: 224.0540

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
224.057g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
222.963g/mol
Monoisotopic Mass:
222.963g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
227
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


5-Bromoquinolin-2(1H)-one is a versatile compound used in chemical synthesis as a key building block in the production of various pharmaceuticals, agrochemicals, and materials. Its unique structure and reactivity make it a valuable intermediate in organic reactions. This compound can undergo various transformations, such as nucleophilic substitution, oxidation, and cycloaddition reactions, allowing for the synthesis of complex molecules with specific functionalities and properties. In pharmaceutical synthesis, 5-Bromoquinolin-2(1H)-one is utilized in the preparation of antimalarial and antiviral agents, as well as potential drug candidates for various diseases. Additionally, in the field of agrochemicals, this compound serves as a precursor to pesticides and herbicides with broad-spectrum activity. Furthermore, its application extends to materials science, where it is employed in the synthesis of novel polymers and organic materials with tailored properties for diverse applications.