157396-14-0

Basic information

• Product Name: 4-(4-chlorophenylthio)-4-(1-phenylsulfonyl-1H-pyrrol-2-yl)butanoyl chloride
• Synonyms: 4-(4-chlorophenylthio)-4-(1-phenylsulfonyl-1H-pyrrol-2-yl)butanoyl chloride
• CAS NO: 157396-14-0
• Molecular Weight: 454.398
• Mol File: 157396-14-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-(4-chlorophenylthio)-4-(1-phenylsulfonyl-1H-pyrrol-2-yl)butanoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-chlorophenylthio)-4-(1-phenylsulfonyl-1H-pyrrol-2-yl)butanoyl chloride(157396-14-0)
• EPA Substance Registry System: 4-(4-chlorophenylthio)-4-(1-phenylsulfonyl-1H-pyrrol-2-yl)butanoyl chloride(157396-14-0)

Safety Data

• Hazardous Substances Data: 157396-14-0(Hazardous Substances Data)

Upstream product

• 157396-13-9 ethyl 4-(4-chlorophenylthio)-4-(1-phenylsulfonyl-1H-pyrrol-2-yl)butanoate 
• 146564-01-4 ethyl 4-chloro-4-(4-chlorophenylthio)butanoate 
• 16851-82-4 N-phenylsulfonylpyrrole 

Downstream Products

• 157396-11-7 7-(4-chlorophenylthio)-6,7-dihydro-1-(phenylsulfonyl)-1H-indol-4(5H)-one 
• 95969-13-4 1-Benzenesulfonyl-4-hydroxy-1H-indole 
• 146564-00-3 1‐(benzenesulfonyl)‐4‐methoxy‐1H‐indole 
• 79315-62-1 4-(benzyloxy)-1-(phenylsulfonyl)-1H-indole 
• 146564-14-9 methyl <1-(phenylsulfonyl)-1H-indol-4-ylthio>acetate 
• 146564-11-6 methyl 3-methyl-5-phenylsulfonyl-5H-thiopyrano<4,3,2-c,d>indole-2-carboxylate 
• 146564-09-2 methyl <3-acetyl-1-(phenylsulfonyl)-1H-indol-4-ylthio>acetate 
• 157396-16-2 1-Benzenesulfonyl-7-(4-chloro-benzenesulfinyl)-1,5,6,7-tetrahydro-indol-4-one 
• 146564-12-7 1-Benzenesulfonyl-7-(4-chloro-phenylsulfanyl)-4-trimethylsilanyloxy-4,5,6,7-tetrahydro-1H-indole-4-carbonitrile 
• 146564-05-8 1-Benzenesulfonyl-7-(4-chloro-phenylsulfanyl)-4-methyl-4,5,6,7-tetrahydro-1H-indol-4-ol 
• 146564-06-9 4-methyl-1-phenylsulfonyl-1H-indole 

Relevant articles and documents

A new, general entry to 4-substituted indoles. Synthesis of (S)-(-)-pindolol and (±)-chuangxinmycin

A new method for synthesis of 4-substituted indoles has been developed by using the 7-arylthio-6-7-dihydroindol-4(5H) one 5 as a common intermediate. The method was applied to the synthesis of (S)-(-)-pindolol (11) and (±)-chuangxinmycin (16).