5023-67-6

Basic information

• Product Name: 1-methoxy-4-[(phenylsulfanyl)methyl]benzene
• CAS NO: 5023-67-6
• Molecular Formula: C₁₄H₁₄OS
• Molecular Weight: 230.3254
• Mol File: 5023-67-6.mol
• Article Data: 37

Chemical Properties

• Boiling Point: 356.1°C at 760 mmHg
• Flash Point: 169.2°C
• Density: 1.13g/cm³
• Vapor Pressure: 6.12E-05mmHg at 25°C
• Refractive Index: 1.61
• CAS DataBase Reference: 1-methoxy-4-[(phenylsulfanyl)methyl]benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methoxy-4-[(phenylsulfanyl)methyl]benzene(5023-67-6)
• EPA Substance Registry System: 1-methoxy-4-[(phenylsulfanyl)methyl]benzene(5023-67-6)

Safety Data

• Hazardous Substances Data: 5023-67-6(Hazardous Substances Data)

Usage

General Description

1-methoxy-4-[(phenylsulfanyl)methyl]benzene, also known as p-anisyl phenyl sulfide, is an organic compound with the molecular formula C14H14OS. It is a yellowish to brownish liquid that is insoluble in water but soluble in organic solvents. This chemical is often used in the synthesis of pharmaceuticals and other organic compounds due to its aromatic and sulfur-containing properties. It can also be used as a fragrance in perfumes and other personal care products. Additionally, p-anisyl phenyl sulfide has been studied for its potential as an antibacterial agent and in the field of organic electronics.

Upstream product

• 23837-10-7 ((4-methoxyphenyl)methylene)bis(phenylsulfane) 
• 882-33-7 diphenyldisulfane 
• 3613-53-4 1-((benzyloxy)methyl)-4-methoxybenzene 
• 108-98-5 thiophenol 
• 3111-52-2 potassium thiophenolate 
• 15175-54-9 N,N-dimethyl-4-methoxylbenzylamine 
• 105-13-5 4-Methoxybenzyl alcohol 
• 4551-15-9 phenylthiotrimethylsilane 
• 104-21-2 p-methoxybenzyl acetate 
• 19350-72-2 N'-(4-methoxybenzylidene)-4-methylbenzenesulfonohydrazide 
• 123-11-5 4-methoxy-benzaldehyde 
• 76950-87-3 1-(4-Methoxy-benzyl)-4,6-diphenyl-1H-pyridine-2-thione 
• 824-94-2 p-methoxybenzyl chloride 
• 104330-36-1 p-methoxybenzyl 3-phenylpropyl ether 

Downstream Products

• 104-21-2 p-methoxybenzyl acetate 
• 123-11-5 4-methoxy-benzaldehyde 
• 105-13-5 4-Methoxybenzyl alcohol 
• 882-33-7 diphenyldisulfane 
• 139-66-2 diphenyl sulfide 
• 7605-25-6 ethyl phenylsulfenylacetate 
• 5219-61-4 (phenylthio)acetonitrile 
• 1188287-36-6 C₁₇H₁₈O₂S 
• 34665-81-1 5-hydroxy-5-(4-methoxyphenyl)valeric acid δ lactone 
• 26153-41-3 γ-(4-methoxyphenyl)-γ-butyrolactone 
• 132723-33-2 2-(4-methoxyphenyl)-tetrahydro-2H-pyran 

Relevant articles and documents

Dithioacetalization or thioetherification of benzyl alcohols using 9-mesityl-10-methylacridinium perchlorate photocatalyst

We report herein the use of 9-mesityl-10-methylacridinium perchlorate as the visible-light photocatalyst for dithioacetalization or thioetherification of benzyl alcohols in one pot using aerial dioxygen as a terminal oxidant. EPR analysis and Stern-Volmer

Nanolayered cobalt-molybdenum sulphides (Co-Mo-S) catalyse borrowing hydrogen C-S bond formation reactions of thiols or H2S with alcohols

Nanolayered cobalt-molybdenum sulphide (Co-Mo-S) materials have been established as excellent catalysts for C-S bond construction. These catalysts allow for the preparation of a broad range of thioethers in good to excellent yields from structurally diverse thiols and readily available primary as well as secondary alcohols. Chemoselectivity in the presence of sensitive groups such as double bonds, nitriles, carboxylic esters and halogens has been demonstrated. It is also shown that the reaction takes place through a hydrogen-autotransfer (borrowing hydrogen) mechanism that involves Co-Mo-S-mediated dehydrogenation and hydrogenation reactions. A novel catalytic protocol based on the thioetherification of alcohols with hydrogen sulphide (H2S) to furnish symmetrical thioethers has also been developed using these earth-abundant metal-based sulphide catalysts.

Nano cobalt ferrite catalyzed coupling reaction of nitroarene and alkyl halide: An odorless and ligand-free rout to unsymmetrical thioether synthesis

This study describes an odorless protocol for the synthesis of unsymmetrical sulfides via cobalt ferrite (CoFe2O4) catalyzed cross-coupling reaction of nitroarenes with alkyl halides in the presence of thiourea as sulfur source under