102210-76-4

Basic information

• Product Name: 1H-Indole, 2-(3-methyl-1-oxo-2-butenyl)-1-(phenylsulfonyl)-
• CAS NO: 102210-76-4
• Molecular Formula: C19H17NO3S
• Molecular Weight: 339.415
• Mol File: 102210-76-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 2-(3-methyl-1-oxo-2-butenyl)-1-(phenylsulfonyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 2-(3-methyl-1-oxo-2-butenyl)-1-(phenylsulfonyl)-(102210-76-4)
• EPA Substance Registry System: 1H-Indole, 2-(3-methyl-1-oxo-2-butenyl)-1-(phenylsulfonyl)-(102210-76-4)

Safety Data

• Hazardous Substances Data: 102210-76-4(Hazardous Substances Data)

Upstream product

• 3350-78-5 3,3-Dimethylacryloyl chloride 
• 40899-71-6 1-benzenesulfonylindole 
• 99655-68-2 3-bromo-1-phenylsulfonyl indole 
• 120-72-9 indole 
• 98-09-9 benzenesulfonyl chloride 
• 1484-27-1 3-bromoindole 
• 107-86-8 3,3-dimethyl acrylaldehyde 

Downstream Products

• 581083-28-5 1.1-dimethyl-4-[1-(phenylsulfonyl)]-1,4-dihydrocyclopenta[b]indol-3(2H)-one 
• 102210-78-6 1-(1-Benzenesulfonyl-1H-indol-2-yl)-3-chloro-3-methyl-butan-1-one 

Relevant articles and documents

HEPATITIS C INHIBITOR COMPOUNDS

Compounds of Formula (I) wherein n, X1, X2, R1, R2, Y1, Y2 and RA are defined herein, are useful for the treatment of hepatitis C viral infection.

Efficient synthesis of bromocyclopenta[b]indoles via a bromination - Reduction sequence

Substituted cyclopenta[b]indoles are selectively brominated in good yields with excess pyridine - Br2 charge-transfer complex (PyBr2) in a one-pot reaction to provide 5 and/or 7-bromoindoles. The mechanism involves the formation of a