Nombre del producto:(3-Bromophenyl)(quinolin-4-yl)methanone

IUPAC Name:4-(3-bromobenzoyl)quinoline

CAS:1706429-73-3
Fórmula molecular:C16H10BrNO
Pureza:97%
Número de catálogo:CM263771
Peso molecular:312.17

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CM263771-1g 1-2 Weeks ɐȷȌ

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Detalles del producto

Núm. De CAS :1706429-73-3
Fórmula molecular:C16H10BrNO
Punto de fusión:-
Código de sonrisas:O=C(C1=CC=NC2=CC=CC=C12)C3=CC=CC(Br)=C3
Densidad:
Número de catálogo:CM263771
Peso molecular:312.17
Punto de ebullición:
Nº Mdl:MFCD17170355
Almacenamiento:

Category Infos

Quinolines
Quinolines are an important class of biologically active heterocyclic compounds, and their derivatives usually exhibit a variety of biological activities. They can be used as antimalarial drugs and in the preparation of other antimalarial drugs. Other important activities of quinoline derivatives include inhibitory activity against EGFR-TK and antipsychotic activity. Futhermore, quinoline scaffolds are present in various drug molecules, including the antimalarial drugs aablaquine, chloroquine, mefloquine and primaquine, and the antibacterial agents gatifloxacin, levofloxacin, and moxifloxacin.
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Product Overview (3-Bromophenyl)(quinolin-4-yl)methanone (1706429-73-3) is an organic compound belonging to the quinoline family. It is an important intermediate in the synthesis of various organic compounds such as pharmaceuticals, dyes, and pigments. It is used in the synthesis of a wide range of organic compounds and has a variety of applications in the pharmaceutical and chemical industries.
Physical Properties Appearance: (3-Bromophenyl)(quinolin-4-yl)methanone is a colorless solid.
Melting Point: When in solid form, it typically has a melting point of 91-93°C.
Solubility: The compound is soluble in organic solvents.
Chemical Properties (3-Bromophenyl)(quinolin-4-yl)methanone is a reactive compound, often utilized as a starting material or intermediate in various chemical reactions and synthesis processes.
Synthesis and Application (3-Bromophenyl)(quinolin-4-yl)methanone has been used in a variety of scientific research applications. It has been used as a model compound to study the reactivity of quinoline derivatives in organic synthesis, as well as in the synthesis of pharmaceuticals, dyes, and pigments. It has also been used as a starting material for the synthesis of various organometallic complexes. Additionally, (3-Bromophenyl)(quinolin-4-yl)methanone has been used in the synthesis of novel compounds with potential applications in the treatment of cancer and other diseases.