1371592-09-4

Basic information

• Product Name: 1-[4-(1-benzyl-4-chloroindol-3-yl)-benzo[1,3]dioxol-5-yl]-propan-1-one
• Synonyms: 1-[4-(1-benzyl-4-chloroindol-3-yl)-benzo[1,3]dioxol-5-yl]-propan-1-one
• CAS NO: 1371592-09-4
• Molecular Weight: 417.892
• Mol File: 1371592-09-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-[4-(1-benzyl-4-chloroindol-3-yl)-benzo[1,3]dioxol-5-yl]-propan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[4-(1-benzyl-4-chloroindol-3-yl)-benzo[1,3]dioxol-5-yl]-propan-1-one(1371592-09-4)
• EPA Substance Registry System: 1-[4-(1-benzyl-4-chloroindol-3-yl)-benzo[1,3]dioxol-5-yl]-propan-1-one(1371592-09-4)

Safety Data

• Hazardous Substances Data: 1371592-09-4(Hazardous Substances Data)

Upstream product

• 77801-60-6 4-chloro-1-benzyl-1H-indole 
• 56008-63-0 4-bromobenzo[d][1,3]dioxole-5-carbaldehyde 
• 1371591-88-6 1-benzyl-4-chloro-3-iodoindole 
• 1371591-86-4 1-benzyl-3-bromo-4-chloroindole 
• 1371592-03-8 1-(4-bromo-benzo[1,3]dioxol-5-yl)-propan-1-one 
• 1371591-91-1 1-benzyl-4-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-indole 
• 25235-85-2 4-chloro-1H-indole 

Relevant articles and documents

Synthesis of tetracyclic indoles via intramolecular α-arylation of ketones

Figure Persented: An intramolecular palladium(0)-mediated α-arylation of ketones applied to the synthesis of various substituted tetracyclic indoles is reported. Most significantly, the efficiency of the transformation was enhanced by the use of monoligated Pd(0) complexes. This methodology was extended to double α-arylation of ketones using one-pot reactions with either simultaneous addition or sequential addition of two aryl halides for producing aryl substituted tetracyclic indoles.