138900-59-1

Basic information

• Product Name: 1H-Pyrrole, 3-(4-methoxyphenyl)-1-[tris(1-methylethyl)silyl]-
• CAS NO: 138900-59-1
• Molecular Formula: C20H31NOSi
• Molecular Weight: 329.558
• Mol File: 138900-59-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrole, 3-(4-methoxyphenyl)-1-[tris(1-methylethyl)silyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole, 3-(4-methoxyphenyl)-1-[tris(1-methylethyl)silyl]-(138900-59-1)
• EPA Substance Registry System: 1H-Pyrrole, 3-(4-methoxyphenyl)-1-[tris(1-methylethyl)silyl]-(138900-59-1)

Safety Data

• Hazardous Substances Data: 138900-59-1(Hazardous Substances Data)

Upstream product

• 104-92-7 1-bromo-4-methoxy-benzene 
• 365564-11-0 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(triisopropylsilyl)pyrrole 
• 138900-55-7 1-(triisopropylsilyl)-1H-pyrrole-3-boronic acid 
• 87630-36-2 3-bromo-1-triisopropylsilanyl-1H-pyrrole 
• 13139-86-1 4-methoxyphenyl magnesium bromide 

Downstream Products

• 63761-14-8 3-(4-Methoxy-phenyl)-1H-pyrrole 
• 773851-40-4 3-bromo-4-(4-methoxyphenyl)-1-(triisopropylsilyl)pyrrole 

Relevant articles and documents

Synthesis of the pyrrolo[2,3-c]carbazole core of the dictyodendrins

The pyrrolo[2,3-c]carbazole 1, the common core of the marine alkaloids known as the dictyodendrins, has been synthesised. The sequence is based on a Suzuki cross-coupling reaction between the pyrrole fragment 2 and the indole fragment 3, followed by tandem photochemical 6π-electrocyclisation/ aromatisation.

Synthesis of 3-Arylpyrroles and 3-Pyrrolylacetylenes by Palladium-Catalyzed Coupling Reactions

Efficacious methods for the synthesis of 3-arylpyrroles or 3-pyrrolylacetylenes are described based on the palladium-catalyzed coupling of appropriate 1-(triisopropylsilyl)-3-substituted pyrroles with aryl halides or monosubstituted acetylenes and subsequ