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Dibenzothiophene, a representative of polycyclic aromatic hydrocarbons (PAHs), holds significant importance in various contexts. Its hydrodesulfurization kinetics on a presulfided molybdenaalumina catalyst have been extensively examined in a high-pressure-flow microreactor. Moreover, the biodesulfurization of dibenzothiophene, achieved through selective cleavage of carbon-sulfur bonds by the thermophilic bacterium Bacillus subtilis WU-S2B, has been documented. This sulfur-containing PAH, dibenzothiophene, possesses three fused rings and exhibits keratolytic activity. It is notably found as a component of petroleum oils. Dibenzothiophene can be described as a parent compound of a heterotricyclic structure, featuring a thiophene ring flanked by two ortho-fused benzene rings at the 2,3- and 4,5-positions. Dibenzothiophene belongs to the dibenzothiophene family and serves as a core structure within the realm of heterotricyclic organic compounds.
Ordering Information
Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Dibenzothiophene, 1 g | sc-239684 | 1 g | $41.00 |