Produktname:9-Phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole

IUPAC Name:9-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole

CAS:1126522-69-7
Molekulare Formel:C24H24BNO2
Reinheit:97%
Katalognummer:CM136829
Molekulargewicht:369.26

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Produkt-Details

CAS-Nr.:1126522-69-7
Molekulare Formel:C24H24BNO2
Schmelzpunkt:-
SMILES-Code:CC1(OB(C2=CC3=C(C=C2)N(C4=CC=CC=C4)C5=C3C=CC=C5)OC1(C)C)C
Dichte:
Katalognummer:CM136829
Molekulargewicht:369.26
Siedepunkt:478.3°C at 760 mmHg
Mdl-Nr.:MFCD16621140
Lagerung:

Category Infos

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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Carbazoles
Carbazoles are an important class of nitrogen-containing heterocycles with a planar tricyclic skeleton consisting of two benzene rings fused on both sides of the central pyrrole ring, with a large aromatic system and a central nitrogen atom, showing broad of electron delocalization. The structure of this compound is based on the indole structure, but in which a second benzene ring is fused to a five-membered ring at positions 2-3 of the indole. Carbazole structural motifs are widely found in, but not limited to, a large number of natural alkaloids of plant or bacterial origin. Since many of these alkaloids are medically useful, exhibit a fairly wide range of biological activities (anticancer, anti-HIV, antibacterial, anti-Alzheimer's disease, anticoagulant, analgesic, antiepileptic, antidiabetic, antioxidant, etc.). Medicinal chemistry also uses carbazole motifs in synthetic drugs to combat hypertension, heart disease, and hepatitis C virus replication.
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