63296-17-3

Basic information

• Product Name: 1-(4-methoxyphenyl)-2-methyl disulfide
• Synonyms: 1-(4-methoxyphenyl)-2-methyl disulfide
• CAS NO: 63296-17-3
• Molecular Weight: 186.299
• Mol File: 63296-17-3.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1-(4-methoxyphenyl)-2-methyl disulfide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-methoxyphenyl)-2-methyl disulfide(63296-17-3)
• EPA Substance Registry System: 1-(4-methoxyphenyl)-2-methyl disulfide(63296-17-3)

Safety Data

• Hazardous Substances Data: 63296-17-3(Hazardous Substances Data)

Upstream product

• 624-92-0 Dimethyldisulphide 
• 696-63-9 4-Methoxybenzenethiol 
• 5335-87-5 4,4'-dimethoxyphenyl disulfide 

Relevant articles and documents

Disproportionation reaction of disulfides promoted by nitric oxide (NO) in the presence of oxygen

Two disulfides brought about disproportionation reaction to afford an unsymmetrical disulfide in 50% yield with a catalytic amount of nitric oxide in the presence of oxygen. The reaction proceeded faster when alkyl disulfides were employed for the reaction, and the substituent effects suggested that the reaction commenced with an oxidative process.

PdCl2/DMSO-Catalyzed Thiol-Disulfide Exchange: Synthesis of Unsymmetrical Disulfide

Unsymmetrical disulfides have been effectively prepared through thiol exchange with symmetrical disulfides employing a simple PdCl2/DMSO catalytic system. The given method features excellent functional group tolerance, a broad substrate scope, and operational simplicity. This reaction is especially useful for late-stage functionalization of bioactive scaffolds such as peptides and pharmaceuticals. Disulfide-containing organic dyes have also been prepared. This transformation could be extended to thiol-diselenide or thiol-ditelluride exchange affording RS-SeR′ or RS-TeR′.

Method for NFSI-catalyzed synthesis of asymmetric disulphide derivatives

The invention belongs to the field of fine chemical engineering, and relates to a method for NFSI-catalytically synthesizing an asymmetric disulphide derivative, which comprises the following steps: NFSI. The symmetric disulfide A and the symmetric disulf