683203-82-9

Basic information

• Product Name: 1H-Indole, 5-bromo-3-[(4-fluorophenyl)thio]-
• CAS NO: 683203-82-9
• Molecular Formula: C14H9BrFNS
• Molecular Weight: 322.201
• Mol File: 683203-82-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 5-bromo-3-[(4-fluorophenyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 5-bromo-3-[(4-fluorophenyl)thio]-(683203-82-9)
• EPA Substance Registry System: 1H-Indole, 5-bromo-3-[(4-fluorophenyl)thio]-(683203-82-9)

Safety Data

• Hazardous Substances Data: 683203-82-9(Hazardous Substances Data)

Upstream product

• 106-40-1 4-bromo-aniline 
• 371-42-6 4-Fluorothiophenol 
• 61871-82-7 1-(2-amino-5-bromophenyl)-2-chloroethan-1-one 
• 10075-50-0 5-bromo-1H-indole 
• 405-31-2 bis(4-fluorophenyl)disulfide 

Relevant articles and documents

ANTIMICROBIAL COMPOUNDS, COMPOSITIONS, AND ARTICLES OF MANUFACTURE FOR SELECTIVELY INHIBITING PATHOGENIC MICROBES

A compound can have a structure of Formula A, or derivative thereof, salt thereof, or stereoisomer thereof, or having any chirality at any chiral center, or tautomer, polymorph, solvate, or combination thereof: wherein ring A is a phenyl, indolyl, naphthyl, or benzothiazolyl; X is S, SO, or SO2; Y is a linker or bond; Z is CH, CR2, or N; Z1 is C or N to form an imidazopyridine; each Z2, Z3, or Z4 is independently CH, CR2, or N; each Z5 or Z6 is C or CH; each R1, R2, and R3 is independently a substituent, and at least one of R1, R2, or R3 is a substituent other than a hydrogen; m is 0, 1, 2, 3, or 4; and n is 0 or a positive integer. The compounds can have specific substituent patterns.

Metal-free, iodine-catalyzed regioselective sulfenylation of indoles with thiols

An iodine-catalyzed regioselective sulfenylation of indoles in the presence of DMSO has been presented. Various indoles can react with aryl thiols or alkyl thiols to afford their corresponding 3-sulfenylindoles in good to excellent yields. The notable fea