製品名:9,9'-(5-(6-([1,1'-biphenyl]-3-yl)-2-phenylpyrimidin-4-yl)-1,3-phenylene)bis(9H-carbazole)

IUPAC Name:9-[3-(6-{[1,1'-biphenyl]-3-yl}-2-phenylpyrimidin-4-yl)-5-(9H-carbazol-9-yl)phenyl]-9H-carbazole

CAS番号:1492813-34-9
分子式:C52H34N4
純度:95%+
カタログ番号:CM338781
分子量:714.87

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製品詳細

CAS番号:1492813-34-9
分子式:C52H34N4
融点:-
SMILESコード:C1(N2C3=C(C4=C2C=CC=C4)C=CC=C3)=CC(C5=NC(C6=CC=CC=C6)=NC(C7=CC(C8=CC=CC=C8)=CC=C7)=C5)=CC(N9C%10=C(C%11=C9C=CC=C%11)C=CC=C%10)=C1
密度:
カタログ番号:CM338781
分子量:714.87
沸点:
MDL番号:
保管方法:

Category Infos

Pyrimidines
Pyrimidine, also known as 1,3-diazobenzene, is a heterocyclic compound with the chemical formula C4H4N2. Pyrimidine is formed by substituting 2 nitrogen atoms for 2 carbons in the meta-position of benzene. It is a diazine and retains its aromaticity. Derivatives of pyrimidine widely exist in organic macromolecular nucleic acids, and many drugs also contain pyrimidine rings. In nucleic acids, three nucleobases are pyrimidine derivatives: cytosine, thymine and uracil. There are a variety of pyrimidine-containing drugs on the market, most of which are kinase inhibitors.
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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