104636-54-6

Basic information

• Product Name: 5-phenyl-2,3-dihydroindole
• Synonyms: 5-phenyl-2,3-dihydroindole
• CAS NO: 104636-54-6
• Molecular Weight: 195.264
• Mol File: 104636-54-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 5-phenyl-2,3-dihydroindole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-phenyl-2,3-dihydroindole(104636-54-6)
• EPA Substance Registry System: 5-phenyl-2,3-dihydroindole(104636-54-6)

Safety Data

• Hazardous Substances Data: 104636-54-6(Hazardous Substances Data)

Upstream product

• 7633-56-9 N-aminoindoline 
• 71-43-2 benzene 
• 22190-33-6 5-bromoindoline 
• 98-80-6 phenylboronic acid 
• 22190-38-1 5-bromo-N-acetylindoline 
• 10075-50-0 5-bromo-1H-indole 
• 66616-72-6 5-phenyl-1H-indole 

Downstream Products

• 66616-72-6 5-phenyl-1H-indole 
• 884496-37-1 1-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-5-phenylindoline-2,3-dione 
• 884496-36-0 1-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-5-phenylindole 
• 884496-35-9 1-(β-D-glucopyranosyl)-5-phenylindole 
• 884496-34-8 1-(β-D-glucopyranosyl)-5-phenylindoline 

Relevant articles and documents

Using weak interactions to control C-H mono-nitration of indolines

An unprecedented C-H mononitration of indolines either at the -C5 or -C7 positions under mild condition is reported here. The roles of multiple weak interactions and factors such as steric factors, electronic effects, cation-π interactions, and solvent polarity were established, and we achieved a 100% regioselective electrophilic aromatic (EArS) nitration using Cu(NO3)2 or AgNO3.

Synthesis and antiproliferative activities of diversely substituted glycosyl-isoindigo derivatives

In the course of structure-activity relationship studies, diversely substituted 1-(β-D-glucopyranosyl)-isoindigo derivatives were prepared from commercially available indolines. Their antiproliferative activities were evaluated toward a panel of human solid cancer cell lines (PC 3, DLD-1, MCF-7, M4Beu, A549, PA 1), a murine cell line (L929) and a human fibroblast primary culture to get an insight into the substitution pattern required for the best biological potencies.

A TRIFLUOROMETHANESULFONIC ACID-CATALYZED REACTION OF ARYLHYDRAZINES WITH BENZENE

Arylhydrazines reacted with benzene in the presence of trifluoromethanesulfonic acid (TFSA) to give aminobiphenyls.This is a general method for the synthesis of aminobiphenyls.