73271-41-7

Basic information

• Product Name: 1-METHYL-3-[(4-METHYLPHENYL)IMINO]-1,3-DIHYDRO-2H-INDOL-2-ONE
• Synonyms: 1-METHYL-3-[(4-METHYLPHENYL)IMINO]-1,3-DIHYDRO-2H-INDOL-2-ONE;BUTTPARK 130\40-93;(3E)-1-methyl-3-[(4-methylphenyl)imino]-2,3-dihydro-1H-indol-2-one
• CAS NO: 73271-41-7
• Molecular Formula: C₁₆H₁₄N₂O
• Molecular Weight: 250.3
• Mol File: 73271-41-7.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-METHYL-3-[(4-METHYLPHENYL)IMINO]-1,3-DIHYDRO-2H-INDOL-2-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-METHYL-3-[(4-METHYLPHENYL)IMINO]-1,3-DIHYDRO-2H-INDOL-2-ONE(73271-41-7)
• EPA Substance Registry System: 1-METHYL-3-[(4-METHYLPHENYL)IMINO]-1,3-DIHYDRO-2H-INDOL-2-ONE(73271-41-7)

Safety Data

• Hazardous Substances Data: 73271-41-7(Hazardous Substances Data)

Usage

General Description

1-METHYL-3-[(4-METHYLPHENYL)IMINO]-1,3-DIHYDRO-2H-INDOL-2-ONE is a chemical compound with the molecular formula C17H16N2O. It is an indole derivative with a methyl group and a phenylimino group attached to the indole ring. 1-METHYL-3-[(4-METHYLPHENYL)IMINO]-1,3-DIHYDRO-2H-INDOL-2-ONE has potential pharmaceutical applications, particularly in the field of medicinal chemistry and drug discovery. Its unique chemical structure makes it a promising candidate for the development of new drugs targeting various biological processes. Further research and investigation are necessary to fully understand the potential uses and effects of this compound.

Upstream product

• 1128-44-5 4-methyl-1H-indole-2,3-dione 
• 106-49-0 p-toluidine 
• 2058-74-4 1-methyl-1H-indole-2,3-dione 

Downstream Products

• 3893-33-2 benzil monoazine 
• 96859-88-0 C₃₀H₂₄N₂O₂ 
• 1210949-03-3 diisopropyl 3-(p-tolylamino)-1-methyl-2-oxoindolin-3-ylphosphonate 
• 1210948-84-7 diethyl 1-methyl-2-oxo-3-(p-tolylamino)indolin-3-ylphosphonate 

Relevant articles and documents

Some organotellurium(iv) complexes of 1-methyl-3-(p-tolylimino)indolin-2-one schiff base

Six new hexa-coordinated organotellurium(IV) complexes of type RTeCl3 NMeIPT and R2TeCl2 NMeIPT (R = 4-hydroxyphenyl, 4- methoxyphenyl or 3-methy-4-hydroxyphenyl; NMeIPT(L) = Schiff base (1-methyl-3-(p-tolylimino)indolin-2-one) derived from condensation o

A copper-catalyzed one-pot, three-component diastereoselective synthesis of 3-spiroazetidinimine-2-oxindoles and their synthetic transformation into fluorescent conjugated indolones

A facile and efficient copper(I)-catalyzed one-pot, three-component diastereoselective synthesis that provides new 3-spiroazetidinimine-2-oxindoles in excellent yield has been accomplished. The 3-spiroazetidinimine-2-oxindoles underwent a facile ring-open

Isatin derivatives, a novel class of transthyretin fibrillogenesis inhibitors

The isatin core structure was found to be a novel chemical scaffold in transthyretin (TTR) fibrillogenesis inhibitor design. Among the series of isatin analogues prepared and tested, the nitro compound 1,3-dihydro-3-[(4-nitrophenyl)imino]-2H-indol-2-one (2r) is as potent as triiodophenol, which is one of the most active known TTR inhibitors. The E/Z stereochemistry of these molecules in solution, elucidated by 1H NMR, does not influence their biological activity. The compounds do not bind to the native tetrameric TTR suggesting that their inhibitory action is independent of the protein binding and stabilization.