Produktname:2-Phenyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline
IUPAC Name:2-phenyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline
- CAS：867164-54-3
- Molekulare Formel：C21H22BNO2
- Reinheit：97%
- Katalognummer：CM124068
- Molekulargewicht：331.22
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Produkt-Details
- CAS-Nr.:867164-54-3
- Molekulare Formel:C21H22BNO2
- Schmelzpunkt:-
- SMILES-Code:CC1(C)C(C)(C)OB(C2=CC=C3C=CC(C4=CC=CC=C4)=NC3=C2)O1
- Dichte:
- Katalognummer:CM124068
- Molekulargewicht:331.22
- Siedepunkt:
- Mdl-Nr.:MFCD22126087
- Lagerung:
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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- Boronic Acids and Esters
- Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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