21305-56-6

Basic information

• Product Name: 1,2-Dithiol-1-ium, 3-(methylthio)-4-phenyl-, iodide
• CAS NO: 21305-56-6
• Molecular Formula: C10H9S3.I
• Molecular Weight: 352.284
• Mol File: 21305-56-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,2-Dithiol-1-ium, 3-(methylthio)-4-phenyl-, iodide(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Dithiol-1-ium, 3-(methylthio)-4-phenyl-, iodide(21305-56-6)
• EPA Substance Registry System: 1,2-Dithiol-1-ium, 3-(methylthio)-4-phenyl-, iodide(21305-56-6)

Safety Data

• Hazardous Substances Data: 21305-56-6(Hazardous Substances Data)

Usage

General Description

1,2-Dithiol-1-ium, 3-(methylthio)-4-phenyl-, iodide is a chemical compound that contains a dithiolium ion with a methylthio and phenyl substituents, and an iodide ion. It is commonly used in organic synthesis as a reagent for the preparation of various organic compounds. 1,2-Dithiol-1-ium, 3-(methylthio)-4-phenyl-, iodide exhibits strong nucleophilic properties due to the presence of sulfur atoms, making it useful in reactions involving carbon-carbon and carbon-heteroatom bond formation. It is also commonly employed as a mild oxidizing agent in chemical reactions. Due to its versatile chemical properties, 1,2-Dithiol-1-ium, 3-(methylthio)-4-phenyl-, iodide finds applications in various industries such as pharmaceuticals, agrochemicals, and materials science.

Upstream product

• 3354-37-8 4-phenyl-1,2-dithiole-3-thione 
• 74-88-4 methyl iodide 
• 98-83-9 isopropenylbenzene 
• 98-82-8 Isopropylbenzene 
• 123-86-4 acetic acid butyl ester 

Downstream Products

• 30165-24-3 3-ethylsulfanyl-2-methyl-5-phenyl-isothiazolium; iodide 
• 30165-25-4 2-ethyl-3-methylthio-5-phenylisothiazolium iodide 
• 18712-05-5 2-methyl-3-methylthio-5-phenylisothiazolium iodide 
• 4434-52-0 N-Phenyl-3,3-bis-2-phenyl-propen-1-imin 
• 4307-93-1 1,1-Bis-methylmercapto-2-phenyl-3-p-tolylimino-prop-1-en 
• 4254-65-3 3,3-Bis(methylthio)-2-phenylacrylaldehyd 
• 33900-48-0 3-(Diethyl-amino)-3-phenyl-propen-methyl-dithionat 
• 30165-59-4 3-tert.-Butylamino-2-phenylpropen-methyldithioat 
• 33900-47-9 3-(Dimethyl-amino)-3-phenyl-propen-methyl-dithionat 
• 52095-96-2 2-Phenyl-3ξ-p-toluidino-prop-2-en-dithiosaeure-methylester 
• 30437-31-1 3-Cyclohexylamino-2-phenylpropen-methyldithioat 
• 33900-51-5 3-(N,N-Cyclohexyl-methylamino)-2-phenyl-propen-(methyl)-dithioat 
• 79887-43-7 7,7-Dimethyl-3-phenyl-7,8-dihydro-6H-thiochromene-2,5-dione 
• 79887-39-1 7,7-Dimethyl-3-phenyl-2-thioxo-2,6,7,8-tetrahydro-thiochromen-5-one 

Relevant articles and documents

N2S2 tetradentate ligands for soft cationic species: preparation of new ligands of potential interest in nuclear medicine

The synthesis of N2S2 tetradentate ligands of the bis-(enaminothioester) type was carried out starting from 3-(methylthio)-3H-1,2-dithiolylium iodides and diamines.The title compounds, which are potential ligands for soft cationic species, can be obtained from 1,3-diaminopropan-2-ol and subsequently modified into the dissymmetrical succinic acid ester of the ligand and N-hydroxysuccinimide.The appendage of such a linking group on the chelating structure should allow further grafting to monoclonal antibodies in view of potential applications in nuclear medicine. 3H-1,2-dithiole-3-thione / 1,3-diaminopropan-2-ol / bis-(enaminothioester) / N2S2 tetradentate ligand / N-hydroxysuccinimidyl ester