112970-73-7

Basic information

• Product Name: 1H-Indole, 4-acetyl-1-[(4-methylphenyl)sulfonyl]-
• CAS NO: 112970-73-7
• Molecular Formula: C17H15NO3S
• Molecular Weight: 313.377
• Mol File: 112970-73-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 4-acetyl-1-[(4-methylphenyl)sulfonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 4-acetyl-1-[(4-methylphenyl)sulfonyl]-(112970-73-7)
• EPA Substance Registry System: 1H-Indole, 4-acetyl-1-[(4-methylphenyl)sulfonyl]-(112970-73-7)

Safety Data

• Hazardous Substances Data: 112970-73-7(Hazardous Substances Data)

Upstream product

• 50614-86-3 1-(1H-indol-4-yl)ethan-1-one 
• 98-59-9 p-toluenesulfonyl chloride 
• 112970-64-6 2-vinyl-3-(tosylamino)phenyl trifluoromethanesulfonate 
• 112970-61-3 2-bromo-3-nitrophenyl trifluoromethanesulfonate 
• 112970-62-4 2-ethenyl-3-nitrophenyl trifluoromethanesulfonate 
• 112970-63-5 2-vinyl-3-aminophenyl trifluoromethanesulfonate 
• 101935-40-4 2-bromo-3-hydroxy-1-nitrobenzene 
• 603-85-0 2-Amino-3-nitrophenol 
• 112970-71-5 4-<<(trifluoromethyl)sulfonyl>oxy>-N-tosylindole 
• 112713-84-5 trimethyl(1-ethoxylvinyl)tin 

Downstream Products

• 1425933-69-2 1-(1-tosyl-1H-indol-4-yl)ethanamine 
• 1425933-65-8 2-(1-(1-tosyl-1H-indol-4-yl)ethyl)isoindoline-1,3-dione 
• 1425933-63-6 (+/-)-4-(1-bromoethyl)-1-tosyl-1H-indole 

Relevant articles and documents

PYRAZOLE DERIVATIVES AS BROMODOMAIN INHIBITORS

The present invention is directed to pyrazole derivatives, pharmaceutical compositions comprising the compounds and the use of the compounds or the compositions in the treatment of various diseases

Palladium-Catalyzed Coupling Reactions of (α-Ethoxyvinyl)trimethylstannane with Vinyl and Aryl Triflates

The palladium-catalyzed cross-coupling reaction of vinyl triflates and halides with (α-ethoxyvinyl)trimethylstannane gives high yields of 2-ethoxy 1,3-dienes, which can be hydrolyzed to the corresponding α,β-unsaturated ketones.Aryl triflates undergo an analogous coupling reaction, providing a facile method for replacing the hydroxyl group of a phenol by an acyl group.The use of (α-ethoxyvinyl)trimethylstannane in palladium-catalyzed carbonylative coupling gives rise to vinyl and aryl α-ethoxyvinyl ketones and indirectly to the corresponding α-diketones (which result from their hydrolysis) and glyoxylates (which result from their ozonolysis).