1253410-37-5

Basic information

• Product Name: 2-(1H-indol-4-yl)phenylamine
• Synonyms: 2-(1H-indol-4-yl)phenylamine
• CAS NO: 1253410-37-5
• Molecular Weight: 208.263
• Mol File: 1253410-37-5.mol

Chemical Properties

• CAS DataBase Reference: 2-(1H-indol-4-yl)phenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1H-indol-4-yl)phenylamine(1253410-37-5)
• EPA Substance Registry System: 2-(1H-indol-4-yl)phenylamine(1253410-37-5)

Safety Data

• Hazardous Substances Data: 1253410-37-5(Hazardous Substances Data)

Upstream product

• 52488-36-5 4-bromo-1H-indole 
• 191171-55-8 2-anilineboronic acid pinacol ester 
• 615-36-1 2-bromoaniline 
• 388116-27-6 indole-4-boronic acid pinacol ester 

Downstream Products

• 1253410-87-5 6-(4-methylphenyl)-6,7-dihydro-4H-indolo[3,4-cd][1]benzazepine 
• 1253410-83-1 6-(4-fluorophenyl)-6,7-dihydro-4H-indolo[3,4-cd][1]benzazepine 
• 1253410-74-0 6-(4-chlorophenyl)-6,7-dihydro-4H-indolo[3,4-cd][1]benzazepine 
• 1253410-77-3 6-(4-nitrophenyl)-6,7-dihydro-4H-indolo[3,4-cd][1]benzazepine 
• 1253410-91-1 6-(4-ethoxyphenyl)-6,7-dihydro-4H-indolo[3,4-cd][1]benzazepine 
• 1253410-97-7 2-(6,7-dihydro-4H-indolo[3,4-cd][1]benzazepin-6-yl)phenol 
• 1253410-80-8 6-(4-bromophenyl)-6,7-dihydro-4H-indolo[3,4-cd][1]benzazepine 
• 1335242-67-5 C₂₁H₁₅ClN₂ 
• 1335242-85-7 C₂₃H₁₈N₂O₂ 
• 1335242-81-3 C₂₂H₁₈N₂ 
• 1335242-83-5 C₂₁H₁₆N₂ 
• 1448038-50-3 3-[2-(p-tolylethynyl)phenyl]-3,4-dihydro-1H-benzo[6,7]azepino[3,4,5-cd]indole 

Relevant articles and documents

Catalytic asymmetric pictet-spengler-type reaction for the synthesis of optically active indolo[3,4-cd][1]benzazepines

A new strategy has been introduced to develop a catalytic asymmetric Pictet-Spengler-type reaction by replacing the aldehyde with an imine. A range of 4-(2-aminoaryl)indoles smoothly undergo the chiral phosphoric acid catalyzed asymmetric Pictet-Spengler-

Water-accelerated cationic π-(7-endo) cyclisation: Application to indole-based peri-annulated polyheterocycles

An efficient and versatile method for the synthesis of indolebased polycyclic indolo-benzazepine and its derivatives through water-accelerated cationic π-cyclisation is described. The strategy involves condensation of arylamine moieties linked to C-4 in i