Nom du produit:Methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline-8-carboxylate

IUPAC Name:methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline-8-carboxylate

CAS:1627722-90-0
Formule moléculaire:C17H20BNO4
Pureté:97%
Numéro de catalogue:CM210778
Poids moléculaire:313.16

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Détails du produit

N° CAS:1627722-90-0
Formule moléculaire:C17H20BNO4
Point de fusion:-
Code SMILES:O=C(C1=C2N=CC=CC2=C(B3OC(C)(C)C(C)(C)O3)C=C1)OC
Densité:
Numéro de catalogue:CM210778
Poids moléculaire:313.16
Point d'ébullition:
N° Mdl:
Stockage:

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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