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3-IMINO-2-INDOLINONE is a heterocyclic chemical compound with the molecular formula C9H6N2O. It features an indolinone backbone and a terminal imine group, which contribute to its unique structure and reactivity. 3-IMINO-2-INDOLINONE has garnered interest due to its potential biological activities, particularly as a prospective anti-cancer agent. Additionally, it has been considered for use in organic synthesis and as a building block in the creation of pharmaceuticals and agrochemicals, making it a significant subject for further research and development in medicinal chemistry and chemical synthesis.

612-53-3

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612-53-3 Usage

Uses

Used in Pharmaceutical Industry:
3-IMINO-2-INDOLINONE is used as a potential anti-cancer agent for its possible role in combating cancer cells. Its unique structure allows it to be a candidate for further exploration and development in the field of oncology.
Used in Organic Synthesis:
3-IMINO-2-INDOLINONE is utilized as a building block in the synthesis of various organic compounds. Its reactivity and structural properties make it a valuable component in the creation of complex organic molecules.
Used in Agrochemicals:
3-IMINO-2-INDOLINONE is employed as a starting material or intermediate in the development of agrochemicals. Its potential applications in this industry highlight its versatility and importance in chemical research and product development.

Check Digit Verification of cas no

The CAS Registry Mumber 612-53-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 612-53:
(5*6)+(4*1)+(3*2)+(2*5)+(1*3)=53
53 % 10 = 3
So 612-53-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O/c9-7-5-3-1-2-4-6(5)10-8(7)11/h1-4H,(H2,9,10,11)

612-53-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-aminoindol-2-one

1.2 Other means of identification

Product number -
Other names 2-Indolinone, 3-imino-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:612-53-3 SDS

612-53-3Relevant academic research and scientific papers

Electrochemical characterization of isatin-thiosemicarbazone derivatives

Bandeira, Katlen Christian Tribuzy,Bohs, Lucas Martins Correa,Bresolin, Leandro,Gervini, Vanessa Carratu,Godoi, Marcelo,Justim, Juliano da Rosa,Martins, Bianca Barreto,Melo, Ana Paula Lopes de,Peixoto, Carlos Roberto de Menezes

, (2021/11/26)

Abstract: Herein, we have notably described the electrochemical behavior of four isatin-thiosemicarbazone derivatives. In this regard, cyclic voltammograms of isatin-3-thiosemicarbazone (ITSC), isatin-3-(N4-benzylthiosemicarbazone) (ITSC-Ph), 1-(5-nitro-2-oxoindolin-3-ylidene)thiosemicarbazide (NO2-ITSC) and 1-(5-nitro-2-oxoindolin-3-ylidene)-4-phenylthiosemicarbazide (NO2-ITSC-Ph) have demonstrated an irreversible oxidation process. More specifically, the generation of isatin and thiourea moieties as the final oxidation products was proposed. The cyclic voltammograms also demonstrate irreversible reduction processes of ITSC and ITSC-Ph in three steps. The proposed final products are 3-aminoindolin-2-one and thiourea moieties. In the cyclic voltammograms of NO2-ITSC and NO2-ITSC-Ph, five reduction processes were observed: three of them due to reduction of the nitro group. It was proposed that the formation of 5-hydroxyamino-3-iminoindolin-2-one and the thiourea moieties would be the final products. Graphic abstract: [Figure not available: see fulltext.] Electrochemical characterization of four isatin thiosemicarbazone derivatives is described. The compounds are irreversibly oxidized and reduced. Isatin moieties and thiourea are proposed to be the products generated after oxidation. Considering the reduction processes, the nitro group present at the isatin moiety is also reduced and influences the reduction products generated.

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