33244-57-4

Basic information

• Product Name: 7-Benzoylindoline
• Synonyms: 7-Benzoylindoline;indolin-7-yl(phenyl)methanone
• CAS NO: 33244-57-4
• Molecular Formula: C₁₅H₁₃NO
• Molecular Weight: 223.27
• Mol File: 33244-57-4.mol
• Article Data: 13

Chemical Properties

• Melting Point: 124°C
• Boiling Point: 364.56°C (rough estimate)
• Appearance: /
• Density: 1.0707 (rough estimate)
• Refractive Index: 1.5500 (estimate)
• Water Solubility: 2.29mg/L(25 oC)
• CAS DataBase Reference: 7-Benzoylindoline(CAS DataBase Reference)
• NIST Chemistry Reference: 7-Benzoylindoline(33244-57-4)
• EPA Substance Registry System: 7-Benzoylindoline(33244-57-4)

Safety Data

• Hazardous Substances Data: 33244-57-4(Hazardous Substances Data)

Upstream product

• 496-15-1 1-indoline 
• 611-73-4 Benzoylformic acid 
• 98-88-4 benzoyl chloride 
• 61589-14-8 N-benzoylindoline 
• 100-47-0 benzonitrile 

Downstream Products

• 76049-83-7 7-benzoyl-1-methylindoline 
• 76049-81-5 3-chloro-7-benzoylindole 
• 61941-56-8 2-amino-3-benzoylbenzeneacetic acid,sodium salt 
• 51135-38-7 7-benzoyl-1,3-dihydroindol-2-one 
• 129041-57-2 (3S)-1-phenyl-3-<(S)-phenylalanyl>amino-3,4,5,7-tetrahydropyrrolo<3,2,1-jk><1,4>benzodiazepin-4(3H)-one 
• 129041-56-1 (3R)-1-phenyl-3-<(S)-phenylalanyl>amino-3,4,5,7-tetrahydropyrrolo<3,2,1-jk><1,4>benzodiazepin-4(3H)-one 
• 129042-20-2 (3RS)-3,4,6,7-tetrahydro-3-hydroxy-4-oxo-1-phenylpyrrolo[3,2,1-jk][1,4]benzodiazepine 
• 126149-54-0 (RS)-3-amino-5-phenyl-3,4,6,7,-tetrahydropyrrolo<3,2,1-jk><1,4>benzodiazepin-4(3H)-one 
• 1026903-25-2 Methanesulfonic acid 4-oxo-1-phenyl-3,4,6,7-tetrahydro-[1,4]diazepino[6,7,1-hi]indol-3-yl ester 
• 129042-15-5 Acetic acid 4-oxo-1-phenyl-3,4,6,7-tetrahydro-[1,4]diazepino[6,7,1-hi]indol-3-yl ester 
• 129042-12-2 2-Oxy-1-phenyl-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-one 
• 126167-36-0 1-phenyl-6,7-dihydro[1,4]diazepino[6,7,1-hi]indole-3,4-dione 3-oxime 

Relevant articles and documents

Direct and site-selective palladium-catalyzed c-7 acylation of indolines with aldehydes

The palladium-catalyzed oxidative acylation of indolines at the C-7 position with aldehydes or alcohols via C-H bond activation is described. This protocol represents a facile access to 7-acylated indolines, which can be readily transformed into 7-acylated indoles with diverse biological properties.

Selective C-H Olefination of Indolines (C5) and Tetrahydroquinolines (C6) by Pd/S,O-Ligand Catalysis

Herein, we report a highly selective C-H olefination of directing-group-free indolines (C5) and tetrahydroquinolines (C6) by Pd/S,O-ligand catalysis. In the presence of the S,O-ligand, a wide range of challenging indolines, tetrahydroquinolines, and olefins was efficiently olefinated under mild reaction conditions. The synthetic potential of this methodology was demonstrated by the efficient olefination of several indoline-based natural products.

METHOD OF PREPARING LIGAND COMPOUND AND TRANSITION METAL COMPOUND

The present invention relates to a method of preparing a ligand compound and a transition metal compound comprising the same. An olefin based polymer with excellent material properties can be obtained using the transition metal compound obtained by said m