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3-[2-(2,4-dinitrophenyl)hydrazino]-2H-indol-2-one is a complex organic compound with the molecular formula C10H7N5O5. It is a derivative of indole, a heterocyclic aromatic organic compound, and features a hydrazino group attached to the 2-position of the indole ring. The compound is characterized by the presence of two nitro groups (-NO2) at the 2 and 4 positions of a phenyl ring, which is connected to the hydrazino group. This chemical structure endows the compound with potential applications in various fields, such as pharmaceuticals and chemical research, due to its unique reactivity and properties. However, it is important to note that the compound may have hazardous properties and should be handled with care, following proper safety protocols.

2058-71-1

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2058-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2058-71-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2058-71:
(6*2)+(5*0)+(4*5)+(3*8)+(2*7)+(1*1)=71
71 % 10 = 1
So 2058-71-1 is a valid CAS Registry Number.

2058-71-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[2-(2,4-dinitrophenyl)hydrazinyl]indol-2-one

1.2 Other means of identification

Product number -
Other names -

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

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More Details:2058-71-1 SDS

2058-71-1Relevant academic research and scientific papers

Effect of a =X-NH-Fragment, (X = C, N), on Z/E Isomerization and ON/OFF Functionality of Isatin Arylhydrazones, ((Arylamino)Methylene)Indolin-2-Ones and Their Anions

?andrik, Róbert,Csicsai, Klaudia,Donovalová, Jana,Gáplovsky, Anton,Sokolík, Róbert,Tisovsky, Pavol

, (2020/07/25)

The subject of this work was the study of thermally and photochemically stimulated Z ? E isomerization and hydrazo ? azo tautomerism of Z- and E-isomers of isatin arylhydrazones and ((arylamino)methylene)indolin-2-ones and their anions. Using NMR, UV-Vis spectroscopy, kinetic measurements, and HPLC, we studied the relationship of structure, (Z- and E-isomers), of these compounds and hydrazo=azo tautomerism. The ON/OFF functionality of these compounds and their anions using light to stimulate switching between ON and OFF states was investigated. We pointed out the characterization of the effect of =N- and =CH- structural fragments and aryl structure on ON and OFF states of isatin arylhydrazones and ((arylamino)methylene)indolin-2-ones.

Catalyst free, multicomponent-tandem synthesis of spirooxindole-indazolones and spirooxindole-pyrazolines: A glycerol mediated green approach

Singh, Swastika,Saquib, Mohammad,Singh, Shyam Babu,Singh, Mandavi,Singh, Jagdamba

, p. 45152 - 45157 (2015/06/02)

The development of a versatile new one pot, catalyst free, multicomponent-tandem strategy for assembly of spirooxindole-indazolones and spirooxindole-pyrazolines is described. The reported protocol includes several advantages like environmental friendliness, cost effectiveness, high atom economy, short reaction times and high yields. The reported method is the first green synthesis of spirooxindole-indazolones and spirooxindole-pyrazolines. This journal is

Investigation of reactions between binucleophilic reagents with 2-(2-Oxindolin-3-ylidene)malononitrile derivatives

Seifi, Mohammad,Sheibani, Hassan

, p. 478 - 481 (2013/08/23)

Nucleophilic addition of hydrazines and thiosemicarbazide to the 2-(2-oxoindolin-3-ylidene) malononitrile derivatives 1, followed by elimination of malononitrile, lead to 3-(2-Arylhydrazono)indolin-2-ones and 1-(2-oxoindolin-3- ylidene)thiosemicarbzides r

Synthesis and antibacterial screening of hydrazones, Schiff and Mannich bases of isatin derivatives

Sridhar, Seshaiah Krishnan,Saravanan, Muniyandy,Ramesh, Atmakuru

, p. 615 - 625 (2007/10/03)

Schiff bases and hydrazones of substituted isatins (1-28) were prepared by reacting isatin and aromatic primary amines/hydrazines. A new series of the corresponding N-Mannich base (29-35) was synthesised by reacting them with formaldehyde and diphenyl ami

Hydrazone derivatives and their use

-

, (2008/06/13)

A method of antagonizing the biological effects of an excitatory amino acid of a subject in need of such antagonization, comprising the step of administering to said subject an effective excitatory amino acid antagonizing amount of an indole-2,3-dione-3-h

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