carbazole

In the third step this compound is oxidized by Red lead to carbazole itself.

It is able to degrade carbazole and as such may be used in bioremediation.

It is in both the imidazole and carbazole families of heterocyclic compounds.

A second method for the synthesis of carbazole is the Graebe-Ullmann reaction.

The Bucherer carbazole synthesis is a related organic reaction.

This enzyme catalyses the third step in the aerobic degradation pathway of carbazole.

Commercial anthracene is obtained from coal tar, common impurities being phenanthrene and carbazole.

A classic laboratory organic synthesis for carbazole is the Borsche-Drechsel cyclization.

Carbazole is an aromatic heterocyclic organic compound.

This enzyme participates in carbazole degradation.

P. resinovorans can degrade carbazole.

Carbazole 1,9a-dioxygenase catalyses the first reaction in the pathway of carbazole degradation.

Likewise, the compounds with two benzene rings fused to the central heterocycle are carbazole, acridine, and dibenzoazepine.

In 1992, Gaudiana et al. reported a series of polymethylacrylate compounds containing lateral brominated and iodinated carbazole rings.

This genus, along with genera Clausena and Glycosmis within the same family, are a major source of carbazole alkaloids.

The triazole is unstable and at elevated temperatures nitrogen is set free and the carbazole is formed.

Carbazole derivatives (ondansetron)

Some simple indole alkaloids do not contain tryptamine, such as gramine and glycozoline (the latter is a derivative of carbazole).

There are also purely structural classifications based on the presence of carbazole, β-carboline or other units in the carbon skeleton of the alkaloid molecule.

Fusion of two benzene rings gives rise to a third large family of compounds, respectively the acridine, dibenzothiophene, carbazole, and dibenzofuran.

The Bucherer carbazole synthesis is a chemical reaction used to synthesize carbazoles from naphthols and aryl hydrazines using sodium bisulfite.

This enzyme participates in 3 metabolic pathways: benzoate degradation via hydroxylation, carbazole degradation, and nitrogen metabolism.

In addition, both oxygen and nitrogen heterocyclic hydrocarbons, such as parent and alkyl homologues of carbazole, quinoline, and pyridine, are present in many crude oils.

A 2011 study of girinimbine, a carbazole alkaloid isolated from this plant, found that it inhibited the growth and induced apoptosis in human hepatocellular carcinoma, HepG2 cells in vitro.

TPD (tetraphenyldiaminophenyl) based materials are known to exhibit higher charge carrier mobilities and lower ionization potentials compare to carbazole based (PVK) materials.