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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, 3-bromo-1-methyl-

Brc1cc2ccccc2n(c1=O)C Request for Quotation
Chemical Name: 2(1H)-Quinolinone, 3-bromo-1-methyl-
CAS Number: 941-91-3
Product Number: AG006PA7(AGN-PC-0JO10S)
Synonyms:
MDL No:
Molecular Formula: C10H8BrNO
Molecular Weight: 238.0806

Identification/Properties

Properties
BP:
299.5 °C at 760 mmHg
Storage:
2-8℃;
Computed Properties
Molecular Weight:
238.084g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
236.979g/mol
Monoisotopic Mass:
236.979g/mol
Topological Polar Surface Area:
20.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
262
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Bromo-1-methylquinolin-2(1H)-one, also known as $name$, is a versatile chemical reagent that finds widespread application in chemical synthesis. This compound serves as a valuable building block in the development of various organic molecules, making it an essential tool in the field of medicinal chemistry and drug discovery. One key application of 3-Bromo-1-methylquinolin-2(1H)-one is its use as a precursor in the synthesis of biologically active compounds. By leveraging the reactivity of the bromine atom and the quinoline ring system, chemists can introduce functional groups and structural motifs that are crucial for enhancing the desired biological activity of the final product. Furthermore, the unique structural features of 3-Bromo-1-methylquinolin-2(1H)-one make it a valuable intermediate in the preparation of heterocyclic scaffolds, which are prevalent in a wide range of pharmaceuticals, agrochemicals, and materials science applications. Its ability to undergo various chemical transformations under mild reaction conditions enables the efficient construction of complex molecular architectures with high precision.In addition, the presence of the bromine moiety in 3-Bromo-1-methylquinolin-2(1H)-one allows for further diversification through cross-coupling reactions, halogenation, and other functional group manipulations. This flexibility in derivatization enables chemists to tailor the properties of the final compound for specific purposes, such as improving solubility, stability, or target binding affinity.Overall, 3-Bromo-1-methylquinolin-2(1H)-one serves as a valuable synthetic tool for chemists seeking to access new chemical entities with potential applications in drug development, material science, and beyond. Its versatile reactivity and structural characteristics make it an indispensable component in the toolbox of synthetic chemists striving to innovate and advance the frontiers of chemical research.