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ethyl 4-(7-oxo-9-selena-8-azabicyclo[4.3.0]nona-1,3,5-trien-8-yl)benzo ate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81743-93-3

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81743-93-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81743-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,7,4 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 81743-93:
(7*8)+(6*1)+(5*7)+(4*4)+(3*3)+(2*9)+(1*3)=143
143 % 10 = 3
So 81743-93-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H13NO3Se/c1-2-20-16(19)11-7-9-12(10-8-11)17-15(18)13-5-3-4-6-14(13)21-17/h3-10H,2H2,1H3

81743-93-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-(3-oxo-1,2-benzoselenazol-2-yl)benzoate

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

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

More Details:81743-93-3 SDS

81743-93-3Relevant academic research and scientific papers

Benzisoselenazolone derivative and preparation method and application thereof

-

, (2022/01/05)

The invention provides a benzisoselenazolone derivative and a preparation method and application thereof. The compound has a structure as shown in a formula I. The invention further relates to a preparation method of the compound with the structure shown in the formula I, a pharmaceutical composition and application of the compound in preparation of anti-SARS-CoV-2Mpro drugs.

Synthesis of a Hybrid between SOD Mimetic and Ebselen to Target Oxidative Stress

Orth, Nicole,Scheitler, Andreas,Josef, Verena,Franke, Alicja,Zahl, Achim,Ivanovi?-Burmazovi?, Ivana

, p. 3073 - 3075 (2019/07/15)

Oxidative stress emerged as target in drug discovery due to its diverse role in various diseases, such as cardiovascular, neurodegenerative, and autoimmune diseases. During the last decades, considerable progress was made in the development of compounds with the ability to reduce reactive oxygen species (ROS) like superoxide. However, the dismutation of the latter leads to formation of another harmful ROS, hydrogen peroxide, which can be depleted through peroxidase activity. The present work describes the synthesis of a hybrid, which unifies a superoxide dismutase mimetic, MnIIpyane, and a glutathione peroxidase mimetic, ebselen, that are connected via an amide bond. This unique hybrid is designed in order to convert superoxide into oxygen and water, i.e. as a potential biological agent for complete ROS removal and will be used in the future as mechanistic molecular tool for further elucidation of (patho) physiological consequences of ROS removal.

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