Product Name:2-(2-Chloroquinazolin-4-yl)-9-phenyl-9H-carbazole

IUPAC Name:2-(2-chloroquinazolin-4-yl)-9-phenyl-9H-carbazole

CAS:1616499-37-6
Molecular Formula:C26H16ClN3
Purity:97%
Catalog Number:CM210707
Molecular Weight:405.89

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Product Details

CAS NO:1616499-37-6
Molecular Formula:C26H16ClN3
Melting Point:-
Smiles Code:ClC1=NC(C2=CC(N(C3=CC=CC=C3)C4=C5C=CC=C4)=C5C=C2)=C6C=CC=CC6=N1
Density:
Catalog Number:CM210707
Molecular Weight:405.89
Boiling Point:528.9±50.0°C at 760 mmHg
MDL No:
Storage:Keep in inert atmosphere, store at 2-8°C.

Category Infos

Quinazolines
Quinazolines belong to heterocyclic chemistry, also known as 1,3-naphthalenes. The backbone consists of two six-membered aromatic rings fused to each other, with two nitrogen atoms at positions 1 and 3 on the backbone. The presence of these two nitrogen atoms in quinazoline increases its importance in pharmaceutical and biological reactions. Quinazolines and their derivatives are among the most important heterocyclic compounds due to their diverse chemical reactivity and important range of biological 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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