831-30-1

Basic information

• Product Name: 3H-1,2-Dithiol-3-one, 5-(4-methoxyphenyl)-
• CAS NO: 831-30-1
• Molecular Formula: C10H8O2S2
• Molecular Weight: 224.304
• Mol File: 831-30-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3H-1,2-Dithiol-3-one, 5-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3H-1,2-Dithiol-3-one, 5-(4-methoxyphenyl)-(831-30-1)
• EPA Substance Registry System: 3H-1,2-Dithiol-3-one, 5-(4-methoxyphenyl)-(831-30-1)

Safety Data

• Hazardous Substances Data: 831-30-1(Hazardous Substances Data)

Upstream product

• 24393-56-4 ethyl p-methoxycinnamate 
• 24393-56-4 ethyl (E)-3-(4-methoxyphenyl)prop-2-enoate 
• 532-11-6 anethole trithione 

Downstream Products

• 133430-71-4 5-(p-hydroxyphenyl)-3H-1,2-dithiole-3-one 
• 532-11-6 anethole trithione 
• 95876-30-5 3-(4-methoxy-phenyl)-5-methylsulfanyl-[1,2]dithiolylium; methyl sulfate 
• 19652-13-2 5-amino-3-(4-methoxylphenyl)-1-phenyl-1H-pyrazole 
• 112161-79-2 5-p-methoxy-3-acetoxythiophene 
• 112161-81-6 2-nitroso-3-hydroxy-5-(p-methoxyphenyl)thiophene 
• 112161-80-5 5-p-methoxyphenyl-3-hydroxythiophene 
• 77654-79-6 α-(diethylamino-5 phenyl-4 oxathiole-1,3 ylidene-2) p-methoxythioacetophenone 
• 112161-78-1 (β-p-methoxyphenyl-β-carboxymethylthio)acryloylthioglycolic acid 

Relevant articles and documents

DESMETHYLANETHOLE TRITHIONE DERIVATIVES FOR THE TREATMENT OF DISEASES LINKED TO MITOCHONDRIAL REACTIVE OXYGEN SPECIES (ROS) PRODUCTION

The present invention relates to desmethylanethole trithione ( AOX ) and derivatives thereof, especially derivatives of formula (I), for the prevention and treatment of diseases whose initiation and/or evolution relates to the production and effects of re

SYNTHESIS OF SUBSTITUTED THIENOTHIAZOLES AND INDOLOTHIAZOLES

Alkylene-, halo-, and aryl-substituted 2-methylthienothiazoles were obtained by the action of phosphorus pentasulfide on the corresponding 2-acetylamino-3-bromo- or 2-acetylamino-3-hydroxythiophenes in an organic solvent with heating. 2-Oximes of halo- and methyl-substituted isatins were converted by reduction and acetylation into 2-hydroxy-3-acetylaminoindoles, from which 2-methylindolo-thiazoles were obtained by the action of phosphorous pentasulfide with heating in xylene.