Название продукции:2,7-Diphenyl-9H-carbazole

IUPAC Name:2,7-diphenyl-9H-carbazole

CAS:42448-04-4
Молекулярная формула:C24H17N
Чистота:95%+
Номер в каталоге:CM396227
Молекулярная масса:319.41

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Информация о продукции

Номер CAS:42448-04-4
Молекулярная формула:C24H17N
Точка плавления:-
Smiles-код:N1C2=CC(=CC=C2C2=C1C=C(C=C2)C1=CC=CC=C1)C1=CC=CC=C1
Плотность:
Номер в каталоге:CM396227
Молекулярная масса:319.41
Точка кипения:
Номер Mdl:
Хранение:

Category Infos

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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Product Other Information

Product Overview 2,7-Diphenyl-9H-carbazole (2,7-DPC) is a synthetic compound that has been used in a variety of scientific research applications in the past few decades. It is a member of the carbazole family of compounds.
Physical Properties 2,7-DPC is a colorless solid and is soluble in organic solvents such as ethanol, acetone, and chloroform. It is not very soluble in water, making it difficult to use in aqueous solutions.
Chemical Properties It is a relatively inexpensive compound and is readily available. It is also a stable compound and is not easily degraded by light or heat. It is a relatively non-toxic compound, making it safe for use in lab experiments.
Synthesis and Application 2,7-diphenyl-9H-carbazole has been used in a variety of scientific research applications, including the study of cell signaling pathways, the synthesis of dyes and pharmaceuticals, and the study of the structure and function of proteins. It has also been used in the development of biosensors and in the study of enzyme activity.
Future Directions It could be used to study the structure and function of proteins, as well as to develop new biosensors. It could also be used in the development of new pharmaceuticals, as well as in the study of cell signaling pathways. Additionally, it could be used to study the effects of environmental pollutants on cells and organisms, as well as to study the effects of drugs on cells and organisms. Finally, it could be used to study the effects of diet and lifestyle on health and disease.