30058-45-8

Basic information

• Product Name: (4,5-dimethoxy-2-nitrophenyl)(methyl)sulfane
• Synonyms: (4,5-dimethoxy-2-nitrophenyl)(methyl)sulfane
• CAS NO: 30058-45-8
• Molecular Weight: 229.257
• Mol File: 30058-45-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (4,5-dimethoxy-2-nitrophenyl)(methyl)sulfane(CAS DataBase Reference)
• NIST Chemistry Reference: (4,5-dimethoxy-2-nitrophenyl)(methyl)sulfane(30058-45-8)
• EPA Substance Registry System: (4,5-dimethoxy-2-nitrophenyl)(methyl)sulfane(30058-45-8)

Safety Data

• Hazardous Substances Data: 30058-45-8(Hazardous Substances Data)

Upstream product

• 1444018-10-3 potassium 4,5-dimethoxy-2-nitrobenzoate 
• 67-68-5 dimethyl sulfoxide 
• 4998-07-6 4,5-dimethoxy-2-nitro-benzoic acid 
• 74-93-1 methylthiol 
• 51072-66-3 1-bromo-4,5-dimethoxy-2-nitro-benzene 

Downstream Products

• 68559-74-0 S-methyl-S-<2-<(pyrrolidinylcarbonyl)amino>-4,5-dimethoxyphenyl>sulfoximine 
• 68559-73-9 N-(pyrrolidinylcarbonyl)-2-(methylsulfinyl)-4,5-dimethoxyaniline 
• 68559-72-8 N-(pyrrolidinylcarbonyl)-2-(methylthio)-4,5-dimethoxyaniline 
• 73791-76-1 1-Isocyanato-4,5-dimethoxy-2-methylsulfanyl-benzene 
• 30058-46-9 2-(methylthio)-4,5-dimethoxyaniline 

Relevant articles and documents

Palladium-catalyzed decarboxylative methylthiolation of aromatic carboxylic acids by using DMSO as the sulfurizing reagent

By using simple and readily available DMSO as a convenient and environmentally friendly source of sulfur, a practical approach for the Pd-catalyzed decarboxylative methylthiolation of 2-nitrobenzoic acids was developed. A range of substituents on the aryl group of the ortho-nitrobenzoic acid were compatible with this process.

Synthesis and blood pressure lowering activity of 3-(substituted-amino)-1,2,4-benzothiadazine 1-oxide derivatives

A series of (substituted amino)-1,2,4-benzothiadiazine 1-oxides has been synthesized and most members of the series have been shown to have blood-pressure lowering effects in normotensive rabbits and in spontaneously hypertensive rats. The most active member of the series was 3-[4-(2-furoyl)-1-piperazinyl]-6,7-dimethoxy-1-methyl-1H-1,2,4-benzothiadiazine 1-oxide hydrochloride. This compound in animal tests was equipotent to the known antihypertensive Prazosin.