cas 6209-23-0|| where to buy ethyl 2-(9H-carbazol-9-yl)acetate

Nom du produit:ethyl 2-(9H-carbazol-9-yl)acetate

IUPAC Name:ethyl 2-(9H-carbazol-9-yl)acetate

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CM184998-1g	in stock	ǯșƞ

Pour une utilisation en R&D uniquement..

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: N° CAS:6209-23-0; Formule moléculaire:C16H15NO2; Point de fusion:-; Code SMILES:O=C(OCC)CN1C2=C(C3=C1C=CC=C3)C=CC=C2; Densité:

: Numéro de catalogue:CM184998; Poids moléculaire:253.3; Point d'ébullition:; N° Mdl:MFCD00022224; Stockage:Store at 2-8°C.

: 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.; carbazole price; Buy low price, high quality carbazole,choose our products, warmly welcome new and old customers to visit and patronize!

Product Overview	9-Carbazoleacetic acid ethyl ester is a chemical compound that belongs to the class of carbazole derivatives. It has gained significant attention in the scientific community due to its potential applications in various fields, such as organic electronics, optoelectronics, and medicinal chemistry.
Physical Properties	It is limitations include its low solubility in water and its tendency to degrade under certain conditions.
Chemical Properties	It can be easily synthesized and modified to suit specific needs.
Synthesis and Application	In organic electronics, it has been used as a hole transport material in organic light-emitting diodes (OLEDs) due to its excellent charge transport properties. In optoelectronics, it has been used as a sensitizer in dye-sensitized solar cells (DSSCs) due to its high molar extinction coefficient and broad absorption spectrum. In medicinal chemistry, it has been studied for its potential anticancer and antiviral activities.
Future Directions	Firstly, further research is needed to understand its mechanism of action in biological systems. Secondly, its potential applications in other fields, such as catalysis and materials science, should be explored. Thirdly, its structure-activity relationship should be studied to develop more potent derivatives with improved properties. Lastly, its long-term effects on human health should be investigated to ensure its safety for use in various applications.