343944-91-2

Basic information

• Product Name: benzyl (3-pyridyl) sulfide
• Synonyms: benzyl (3-pyridyl) sulfide
• CAS NO: 343944-91-2
• Molecular Weight: 201.292
• Mol File: 343944-91-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: benzyl (3-pyridyl) sulfide(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl (3-pyridyl) sulfide(343944-91-2)
• EPA Substance Registry System: benzyl (3-pyridyl) sulfide(343944-91-2)

Safety Data

• Hazardous Substances Data: 343944-91-2(Hazardous Substances Data)

Upstream product

• 462-08-8 pyridin-3-ylamine 
• 100-44-7 benzyl chloride 
• 626-55-1 3-Bromopyridine 
• 100-53-8 phenylmethanethiol 
• 6313-36-6 benzyl thiosulphate 

Downstream Products

• 25936-03-2 3-(4-nitrophenylsulfanyl)pyridine 

Relevant articles and documents

SMALL MOLECULE ACTIVATORS OF NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) AND USES THEREOF

Provided herein are small molecule activators of Nicotinamide Phosphoribosyltransferase (NAMPT), compositions comprising the compounds, and methods of using the compounds and compositions.

An aryl alkyl thioether compound and its synthetic method

The invention discloses a synthetic method of an aryl alkyl thioether compound shown as formula (II), and the synthetic method is as follows: at room temperature and in a water phase, using triazene and haloalkane as reaction raw materials, using Na2S2O3 as a vulcanization reagent for reaction under the promotion effect of a copper catalyst and a Lewis acid to obtain the aryl alkyl thioether compound. The advantages of the synthetic method are as follows: reaction is efficient and yield is high; the vulcanization reagent is cheap, easy to obtain, stable, and free of irritating smell; the reaction is carried out in the solvent green water, the reaction is free of addition of a phase transfer catalyst and a volatile organic solvent, and is environmentally friendly; the reaction is carried out at room temperature, is mild in condition; the catalyst copper sulfate used in the reaction is cheap and economic reaction; the reaction substrate is easy in preparation; after amplification, the reaction efficiency is higher.

Sulfide synthesis through copper-catalyzed C-S bond formation under biomolecule-compatible conditions

We report here an efficient and mild method for constructing C-S bonds. The reactions were carried out with Na2S2O3 as a sulfurating reagent, CuSO4 as a catalyst, and water as solvent without any surfactant. The products were achieved in moderate to excellent yields at room temperature under air. Notably, this reaction is compatible with various biomolecules including amino acids, oligosaccharides, nucleosides, proteins, and cell lysates. This journal is