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N-[(E)-2-(3,4-dimethoxyphenyl)-1-{[2-(5-nitro-2-oxo-2H-indol-3-yl)hydrazino]carbonyl}ethenyl]benzamide is a complex organic compound with a molecular formula of C26H22N4O7. It is characterized by a benzamide group attached to a long alkenyl chain, which includes a 3,4-dimethoxyphenyl group and a 5-nitro-2-oxo-2H-indol-3-ylhydrazino moiety. N-[(E)-2-(3,4-dimethoxyphenyl)-1-{[2-(5-nitro-2-oxo-2H-indol-3-yl)hydrazino]carbonyl}ethenyl]benzamide is known for its potential applications in medicinal chemistry, particularly as an inhibitor of certain enzymes or as a precursor in the synthesis of pharmaceuticals. Its structure features a nitro group, which may contribute to its reactivity and potential therapeutic properties. The compound's specific activity and mechanism of action would be detailed in scientific literature and are subject to ongoing research in the field of drug development.

5745-13-1

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5745-13-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5745-13-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,4 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5745-13:
(6*5)+(5*7)+(4*4)+(3*5)+(2*1)+(1*3)=101
101 % 10 = 1
So 5745-13-1 is a valid CAS Registry Number.

5745-13-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(E)-1-(3,4-dimethoxyphenyl)-3-[2-(5-nitro-2-oxoindol-3-yl)hydrazinyl]-3-oxoprop-1-en-2-yl]benzamide

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

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More Details:5745-13-1 SDS

5745-13-1Downstream Products

5745-13-1Relevant academic research and scientific papers

A concerted mechanism for the transfer of the thiophosphinoyl group from aryl dimethylphosphinothioate esters to oxyanionic nucleophiles in aqueous solution

Onyido, Ikenna,Swierczek, Krzysztof,Purcell, Jamie,Hengge, Alvan C.

, p. 7703 - 7711 (2007/10/03)

Earlier work on the hydrolysis of aryl phosphinothioate esters has led to contradictory mechanistic conclusions. To resolve this mechanistic ambiguity, we have measured linear free energy relationships (βnuc and βIg) and kinetic isot

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