Search results
Results from the WOW.Com Content Network
Dibenzyl sulfide is a symmetrical thioether. It contains two C 6 H 5 CH 2 - (benzyl) groups linked by a sulfide bridge. It is a colorless or white solid that is soluble in nonpolar solvents.
Dibenzyl Dihydrostilbene sym-Diphenylethane. Identifiers CAS Number. 103-29-7 ...
This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.
Benzyl is most commonly abbreviated Bn. For example, benzyl alcohol can be represented as BnOH. Less common abbreviations are Bzl and Bz, the latter of which is ambiguous as it is also the standard abbreviation for the benzoyl group C 6 H 5 C(O)−.
Diphenyl disulfide is usually prepared by the oxidation of thiophenol: . 2 PhSH + I 2 → Ph 2 S 2 + 2 HI Hydrogen peroxide can also be used as the oxidant. [2] Ph 2 S 2 is rarely prepared in the laboratory because it is inexpensive, and the precursor has a disagreeable odour.
This page was last edited on 1 February 2024, at 22:19 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
Many methods exist for the preparation of diphenyl sulfide. It arises by a Friedel-Crafts-like reaction of sulfur monochloride and benzene. [4] Diphenyl sulfide and its analogues can also be produced by coupling reactions using metal catalysts. [5]
The 4S pathway is a sulfur-specific metabolic pathway of oxidative desulfurization that converts dibenzothiophene (DBT) into 2-hydroxybiphenyl and sulfite.It uses a total of four NADH molecules (three required by DszD to generate FMNH 2 and a fourth to regenerate the FMN-oxide byproduct of DszA) and three molecules of oxygen, thus producing NAD + and water as byproducts.