1385029-13-9

Basic information

• Product Name: 2-bromo-3-(phenylthio)-1H-indole
• Synonyms: 2-bromo-3-(phenylthio)-1H-indole
• CAS NO: 1385029-13-9
• Molecular Weight: 304.21
• Mol File: 1385029-13-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-bromo-3-(phenylthio)-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-3-(phenylthio)-1H-indole(1385029-13-9)
• EPA Substance Registry System: 2-bromo-3-(phenylthio)-1H-indole(1385029-13-9)

Safety Data

• Hazardous Substances Data: 1385029-13-9(Hazardous Substances Data)

Upstream product

• 120-72-9 indole 
• 2297-65-6 benzenesulfonyl bromide 
• 98-09-9 benzenesulfonyl chloride 
• 108-98-5 thiophenol 
• 882-33-7 diphenyldisulfane 
• 1259577-20-2 N-[2-(2,2-dibromoethenyl)phenyl]methanesulfonamide 

Downstream Products

• 1285494-82-7 2-(4-methoxyphenyl)-3-(phenylthio)-1H-indole 

Relevant articles and documents

Synergistic Dual Role of [hmim]Br-ArSO2Cl in Cascade Sulfenylation-Halogenation of Indole: Mechanistic Insight into Regioselective C-S and C-S/C-X (X = Cl and Br) Bond Formation in One Pot

Bifunctionalized indoles are an important class of biologically active heterocyclic compounds and potential drug candidates. Because of the lack of efficient synthetic methods, one pot cascade synthesis of these compounds is rare and remains a challenge.

An efficient synthesis of 2-bromo(chloro)-3-selenyl(sulfenyl)indoles via tandem reactions of 2-(gem-dibromo(chloro)vinyl)anilines with diselenides(disulfides)

A novel and efficient synthesis of 2-bromo(chloro)-3-selenyl(sulfenyl) indoles through tandem reactions of 2-(gem-dibromo(chloro)vinyl)-N- methylsulfonylanilines with diselenides and disulfides in the presence of t-BuOLi and I2 (10 mol%) in DMS