63157-79-9

Basic information

• Product Name: Disulfide, bis(2,3,5,6-tetramethylphenyl)
• CAS NO: 63157-79-9
• Molecular Formula: C20H26S2
• Molecular Weight: 330.558
• Mol File: 63157-79-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Disulfide, bis(2,3,5,6-tetramethylphenyl)(CAS DataBase Reference)
• NIST Chemistry Reference: Disulfide, bis(2,3,5,6-tetramethylphenyl)(63157-79-9)
• EPA Substance Registry System: Disulfide, bis(2,3,5,6-tetramethylphenyl)(63157-79-9)

Safety Data

• Hazardous Substances Data: 63157-79-9(Hazardous Substances Data)

Upstream product

• 60706-63-0 2,3,5,6-tetramethyl-benzene-1-sulfonyl chloride 
• 95-93-2 1,2,4,5-tetramethylbenzene 
• 111183-90-5 2,3,5,6-tetramethylbenzenesulfenyl chloride 
• 14786-84-6 2,3,5,6-tetramethylthiophenol 

Downstream Products

• 111183-90-5 2,3,5,6-tetramethylbenzenesulfenyl chloride 
• 85479-95-4 {Ru(2,3,5,6-tetramethylbenzenethiolate)4(CH₃CN)} 
• 145514-23-4 {Os(2,3,5,6-tetramethylbenzenethiolate)4(CH₃CN)} 
• 267660-48-0 ethyl (2E,1'R,2'S)-3-[2'-(2,3,5,6-tetramethylphenylthio)cyclopropyl]propenoate 
• 267660-60-6 ethyl (2E,1'R,2'R)-3-[2'-(2,3,5,6-tetramethylphenylthio)cyclopropyl]propenoate 
• 221016-14-4 (2E,1'R,2'S)-3-[2'-(2,3,5,6-tetramethylphenylthio)cyclopropyl]-1-(methylseleno)prop-2-ene 
• 267660-49-1 (2E,1'R,2'S)-3-[2'-(2,3,5,6-tetramethylphenylthio)cyclopropyl]prop-2-en-1-ol 
• 267660-50-4 (2E,1'R,2'R)-3-[2'-(2,3,5,6-tetramethylphenylthio)cyclopropyl]prop-2-en-1-ol 
• 267660-47-9 (1R,2S)-2-(2,3,5,6-tetramethylphenylthio)cyclopropanemethanal 
• 267660-59-3 (1R,2R)-2-(2,3,5,6-tetramethylphenylthio)cyclopropanemethanal 
• 221016-23-5 (1S,2R)-2-(hydroxymethyl)-1-(2,3,5,6-tetramethylphenylthio)cyclopropane 
• 267660-58-2 (1R,2R)-2-(hydroxymethyl)-1-(2,3,5,6-tetramethylphenylthio)cyclopropane 
• 14786-84-6 2,3,5,6-tetramethylthiophenol 

Relevant articles and documents

Attempts to Synthesize Sterically Hindered Thiazyl Arenes and Their Relationship to Arylsulfenyl Nitrenes

Up till now all attempts to synthesize organic thiazyl compounds in substance failed.Stabilization leads to the corresponding disulfide 2, the thioaminyl radical 7 and the sulphur diimide 8.Formally thiazyl compounds 1 and sulfenyl nitrenes 1 were resonance structures.Via sulfenyl nitrenes 1 the formation of 2, 7, 8 can be discussed.An in situ preparation of sulfenyl nitrene 1a via the sulfenyl chloride 5a, synthesized by chlorination of the disulfide 2a, and the sulfenyl azide 6a is described in detail. 1a can also be prepared from the sulfenyl amide 4a by oxidation.The structures of the radicals 7a-f and 12f are discussed.