198062-96-3

Basic information

• Product Name: O-(4-phenoxyphenyl)-N,N-dimethylthiocarbamate
• Synonyms: O-(4-phenoxyphenyl)-N,N-dimethylthiocarbamate
• CAS NO: 198062-96-3
• Molecular Weight: 273.356
• Mol File: 198062-96-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: O-(4-phenoxyphenyl)-N,N-dimethylthiocarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: O-(4-phenoxyphenyl)-N,N-dimethylthiocarbamate(198062-96-3)
• EPA Substance Registry System: O-(4-phenoxyphenyl)-N,N-dimethylthiocarbamate(198062-96-3)

Safety Data

• Hazardous Substances Data: 198062-96-3(Hazardous Substances Data)

Upstream product

• 831-82-3 4-Phenoxyphenol 
• 16420-13-6 N,N-Dimethylthiocarbamoyl chloride 

Downstream Products

• 198062-93-0 S-(4-phenoxyphenyl)-N,N-dimethylthiocarbamate 
• 292605-13-1 3-(4-phenoxyphenylsulfonyl)propyloxirane 
• 292605-12-0 2-(4-phenoxyphenylsulfonyl)ethyloxirane 
• 292605-14-2 SB-3CT 
• 292605-11-9 2-{[(4-phenoxyphenyl)sulfonyl]methyl}oxirane 
• 292605-10-8 5-(4-phenoxyphenylsulfanyl)-1-pentene 
• 292605-09-5 4-(4-phenoxyphenylsulfanyl)-1-butene 
• 3159-49-7 3-(4-phenoxyphenylsulfanyl)-1-propene 
• 38778-05-1 4-(Phenoxy)benzenethiol 

Relevant articles and documents

Electrochemically Catalyzed Newman-Kwart Rearrangement: Mechanism, Structure-Reactivity Relationship, and Parallels to Photoredox Catalysis

The facilitation of redox-neutral reactions by electrochemical injection of holes and electrons, also known as "electrochemical catalysis", is a little explored approach that has the potential to expand the scope of electrosynthesis immensely. To systematically improve existing protocols and to pave the way toward new developments, a better understanding of the underlying principles is crucial. In this context, we have studied the Newman-Kwart rearrangement of O-arylthiocarbamates to the corresponding S-aryl derivatives, the key step in the synthesis of thiophenols from the corresponding phenols. This transformation is a particularly useful example because the conventional method requires temperatures up to 300 °C, whereas electrochemical catalysis facilitates the reaction at room temperature. A combined experimental-quantum chemical approach revealed several reaction channels and rendered an explanation for the relationship between the structure and reactivity. Furthermore, it is shown how rapid cyclic voltammetry measurements can serve as a tool to predict the feasibility for specific substrates. The study also revealed distinct parallels to photoredox-catalyzed reactions, in which back-electron transfer and chain propagation are competing pathways.

An Electrocatalytic Newman-Kwart-type Rearrangement

An electrochemical approach toward rearrangement of O-aryl thiocarbamates to the corresponding S-aryl thiocarbamates is presented. The protocol requires only catalytic amounts of electric charge and allows for operation at room temperature. The electrolys

α-amino-β-sulfonyl hydroxamic acid compounds

A family of molecules is disclosed that inhibit matrix metalloprotease (MMP) activity, and particularly inhibit the activity of one or more of MMP-2, MMP-9, or MMP-13, while generally exhibiting little activity against MMP-1. A contemplated compound also