Product Name:9-ethyl-3-(5-phenyltriazol-1-yl)carbazole

IUPAC Name:9-ethyl-3-(5-phenyl-1H-1,2,3-triazol-1-yl)-9H-carbazole

CAS:2097938-73-1
Molecular Formula:C22H18N4
Purity:95%+
Catalog Number:CM772001
Molecular Weight:338.41

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Product Details

CAS NO:2097938-73-1
Molecular Formula:C22H18N4
Melting Point:-
Smiles Code:CCN1C2=C(C=CC=C2)C2=C1C=CC(=C2)N1N=NC=C1C1=CC=CC=C1
Density:
Catalog Number:CM772001
Molecular Weight:338.41
Boiling Point:
MDL No:MFCD31746894
Storage:

Category Infos

Triazoles
Triazole refers to a heterocyclic compound with the molecular formula C2H3N3, which has a five-membered ring consisting of two carbon atoms and three nitrogen atoms. Neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease already affect many people around the world, and these numbers are increasing rapidly. Treatment for these disorders is often aimed at relieving symptoms and has no cure. Research on new molecules is underway, and heterocyclic compounds have important pharmacological implications. Triazoles and tetrazoles are emerging as new molecules in this field.
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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