120517-33-1

Basic information

• Product Name: 1H-Indole, 2,3-bis(methylthio)-
• CAS NO: 120517-33-1
• Molecular Formula: C10H11NS2
• Molecular Weight: 209.336
• Mol File: 120517-33-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 2,3-bis(methylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 2,3-bis(methylthio)-(120517-33-1)
• EPA Substance Registry System: 1H-Indole, 2,3-bis(methylthio)-(120517-33-1)

Safety Data

• Hazardous Substances Data: 120517-33-1(Hazardous Substances Data)

Upstream product

• 40015-10-9 3-methylthioindole 
• 1440957-15-2 (2-methylthioindol-3-yl)dimethylsulfonium perchlorate 
• 142-84-7 di-n-propylamine 
• 54491-43-9 3-phenylthioindole 
• 5813-48-9 Methanesulfenyl chloride 

Relevant articles and documents

Regioselective synthesis of mixed indole 2,3-bis(sulfides). A study of the mechanism of the second sulfenylation of indole

Sulfenylation of indole using sulfenyl chlorides leads to the initial formation of a 3-indolyl sulfide, while excess reagent introduces a second sulfide at the 2-position of the ring. The mechanism of this second sulfenylation has not, to date, been rigor

Acid-catalysed Isomerization of Indol-3-yl Sulphides to Indol-2-yl Sulphides: Unexpected Intermolecular Nature of the Rearrangement

The rearrangement of indol-3-yl sulphides (1) indol-2-yl sulphides (4), catalysed by proton acids, unexpectedly proceeds by an intermolecular mechanism involving initial disproportionation to an indole-2,3-diyl bis-sulphide (2) and an indole (3), followed by a reaction between (2) and (3) to yield the rearranged product (4).