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2H-Indol-2-one, 1,3-dihydro-3-(4-nitrophenylimino)-, also known as 3-(4-nitrophenylimino)-1,3-dihydro-2H-indol-2-one, is a chemical compound with the molecular formula C14H10N2O3. It is a derivative of indol-2-one, featuring a 1,3-dihydro structure and a 4-nitrophenylimino group attached to the 3-position. 2H-Indol-2-one, 1,3-dihydro-3-(4-nitrophenylimino)- is characterized by its yellow crystalline appearance and is soluble in organic solvents such as ethanol and acetone. It has potential applications in the synthesis of various pharmaceuticals and organic compounds due to its unique structure and reactivity.

78662-38-1

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78662-38-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78662-38-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,6 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78662-38:
(7*7)+(6*8)+(5*6)+(4*6)+(3*2)+(2*3)+(1*8)=171
171 % 10 = 1
So 78662-38-1 is a valid CAS Registry Number.

78662-38-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(4-nitrophenylimino)indolin-2-one

1.2 Other means of identification

Product number -
Other names 3-(4-Nitro-phenylimino)-indolin-2-on

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:78662-38-1 SDS

78662-38-1Downstream Products

78662-38-1Relevant academic research and scientific papers

Leucine rich repeat kinase 2 (LRRK2) inhibitors based on indolinone scaffold: Potential pro-neurogenic agents

Salado, Irene G.,Zaldivar-Diez, Josefa,Sebastian, Victor,Li, Lingling,Geiger, Larissa,González, Silvia,Campillo, Nuria E.,Gil, Carmen,Morales, Aixa V.,Perez, Daniel I.,Martinez, Ana

, p. 328 - 342 (2017/07/07)

Leucine-rich repeat kinase 2 (LRRK2) is one of the most pursued targets for Parkinson's disease (PD) therapy. Moreover, it has recently described its role in regulating Wnt signaling and thus, it may be involved in adult neurogenesis. This new hypothesis

Remote activation of the nucleophilicity of isatin

Zari, Sergei,Kudrjashova, Marina,Pehk, Tonis,Lopp, Margus,Kanger, Tonis

supporting information, p. 1740 - 1743 (2014/04/17)

The concept of the remote activation of reactivity was first applied in asymmetric organocatalysis. An isatin 3-phenylimine derivative acts as a donor in the thiourea catalyzed asymmetric addition to unsaturated 1,4-ketoesters, affording aza-Michael adducts in high enantiomeric purity and yield.

Some isatin Schiff bases as corrosion inhibitors for iron in sulphuric acid solution

Mohamed, A. K.,Bekheit, M. M.,Fouda, A. S.

, p. 331 - 336 (2007/10/02)

Six isatin Schiff bases have been prepared and treated as inhibitors for the corrosion of iron in 1 mol L-1 sulphuric acid.The inhibitor efficiencies calculated from weight loss and polarization methods are in good agreement.The Tafel slope is

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