Название продукции:9-([1,1'-Biphenyl]-3-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
IUPAC Name:9-{[1,1'-biphenyl]-3-yl}-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
- CAS:1533406-38-0
- Молекулярная формула:C30H28BNO2
- Чистота:97%
- Номер в каталоге:CM210395
- Молекулярная масса:445.36
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Информация о продукции
- Номер CAS:1533406-38-0
- Молекулярная формула:C30H28BNO2
- Точка плавления:-
- Smiles-код:CC1(C)C(C)(C)OB(C2=CC3=C(C=C2)N(C4=CC(C5=CC=CC=C5)=CC=C4)C6=C3C=CC=C6)O1
- Плотность:
- Номер в каталоге:CM210395
- Молекулярная масса:445.36
- Точка кипения:578.9±42.0°C at 760 mmHg
- Номер Mdl:MFCD28130384
- Хранение:
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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