142837-80-7

Basic information

• Product Name: 1-(4',6'-dimethoxy-2',3'-diphenylindol-7'-yl)-3-phenylprop-2-en-1-one
• Synonyms: 1-(4',6'-dimethoxy-2',3'-diphenylindol-7'-yl)-3-phenylprop-2-en-1-one
• CAS NO: 142837-80-7
• Molecular Weight: 459.544
• Mol File: 142837-80-7.mol

Chemical Properties

• CAS DataBase Reference: 1-(4',6'-dimethoxy-2',3'-diphenylindol-7'-yl)-3-phenylprop-2-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4',6'-dimethoxy-2',3'-diphenylindol-7'-yl)-3-phenylprop-2-en-1-one(142837-80-7)
• EPA Substance Registry System: 1-(4',6'-dimethoxy-2',3'-diphenylindol-7'-yl)-3-phenylprop-2-en-1-one(142837-80-7)

Safety Data

• Hazardous Substances Data: 142837-80-7(Hazardous Substances Data)

Upstream product

• 91107-10-7 4,6-dimethoxy-2,3-diphenyl-1H-indole 
• 102-92-1 Cinnamoyl chloride 
• 100-52-7 benzaldehyde 
• 142837-78-3 1-(4',6'-dimethoxy-2',3'-diphenylindole-7'-yl)ethanone 
• 102-92-1 cinnamoyl chloride 

Downstream Products

• 193072-49-0 1-(4',6'-dimethoxy-2',3'-diphenylindol-7'-yl)-4-nitro-3-phenylpentan-1-one 
• 142837-82-9 1-(4',6'-dimethoxy-1'-methyl-2',3'-diphenylindol-7'-yl)-4-methyl-4-nitro-3-phenylpentan-1-one 
• 142837-83-0 2-(4',6'-dimethoxy-1'-methyl-2',3'-diphenylindol-7'-yl)-5,5-dimethyl-4-phenyl-1-pyrroline 1-oxide 
• 142837-84-1 2-(4',6'-dimethoxy-1'-methyl-2',3'-diphenylindol-7'-yl)-5,5-dimethyl-4-phenyl-1-pyrroline 
• 142837-81-8 1-(4',6'-dimethoxy-1'-methyl-2',3'-diphenylindol-7'-yl)-3-phenylprop-2-en-1-one 

Relevant articles and documents

Synthesis of pyrroloquinolines as indole analogues of flavonols

7-Acetyl-4,6-dimethoxy-3-phenylindole 10 was converted into a range of 7-indolyl chalcones 13 by reaction with aryl aldehydes under basic conditions. Oxidation of the chalcones 13 with alkaline hydrogen peroxide gave the isolable epoxides 14, which were cyclized with further base treatment into the indole flavonols, or 5-hydroxy-6-oxopyrroloquinolines 15. The related compounds 25 and 26, examples of indole flavanones and flavones, respectively, were also synthesized. UV spectroscopic comparisons between flavonoids and indole flavonoids are discussed.

Nitrones and Oxaziridines. XLIII. Synthesis of an Indol-7-yl-Substituted 1-Pyrroline 1-Oxide and Related Compounds

The pyrroline 1-oxide (8) which contains an indol-7-yl substituent to the 2-position has been synthesized by reductive cyclization of the related γ-nitro ketone.The corresponding 1-pyrroline (9) has also been isolated as the result of non-selective reduct