Nom du produit:9-(4-carbazol-9-yl-6-chloro-1,3,5-triazin-2-yl)carbazole

IUPAC Name:9-[4-(9H-carbazol-9-yl)-6-chloro-1,3,5-triazin-2-yl]-9H-carbazole

CAS:877615-05-9
Formule moléculaire:C27H16ClN5
Pureté:95%+
Numéro de catalogue:CM328854
Poids moléculaire:445.91

Unité d'emballage Stock disponible Prix($) Quantité
CM328854-25g in stock ƙǧɅ

Pour une utilisation en R&D uniquement..

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Détails du produit

N° CAS:877615-05-9
Formule moléculaire:C27H16ClN5
Point de fusion:-
Code SMILES:ClC1=NC(N2C3=C(C4=C2C=CC=C4)C=CC=C3)=NC(N5C6=C(C7=C5C=CC=C7)C=CC=C6)=N1
Densité:
Numéro de catalogue:CM328854
Poids moléculaire:445.91
Point d'ébullition:
N° Mdl:
Stockage:

Category Infos

Triazines
Triazines are an important class of six-membered aromatic heterocycles with three nitrogen atoms that give rise to three regioisomers: 1,2,4-triazines, 1,2,3-triazines, and 1,3, 5-triazine. 1,2,3-Triazines show remarkable reactivity and have attracted attention for their medicinal value. Triazine compounds fused with other carbon and heterocycles are stable and have a broad spectrum of pharmacological activities.
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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