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Benzamide, N-methyl-2-(methylseleno)-N-phenyl-, also known as N-Methyl-N-phenyl-2-(methylseleno)benzamide, is an organic compound with the chemical formula C15H16NOSeS. It is a derivative of benzamide, featuring a methylseleno group (-SeCH3) at the 2-position of the benzene ring and a methyl group (-CH3) at the nitrogen atom. Benzamide, N-methyl-2-(methylseleno)-N-phenyl- is characterized by its unique structure, which combines the properties of benzamide with the presence of selenium and sulfur atoms. It is primarily used in chemical research and as an intermediate in the synthesis of various organic compounds, particularly those involving selenium-containing molecules. Due to its specific functional groups, it may have potential applications in the development of pharmaceuticals, agrochemicals, and other specialty chemicals.

6518-76-9

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6518-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6518-76-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,1 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6518-76:
(6*6)+(5*5)+(4*1)+(3*8)+(2*7)+(1*6)=109
109 % 10 = 9
So 6518-76-9 is a valid CAS Registry Number.

6518-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-2-methylselanyl-N-phenylbenzamide

1.2 Other means of identification

Product number -
Other names Benzamide,N-methyl-2-(methylseleno)-N-phenyl

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:6518-76-9 SDS

6518-76-9Relevant academic research and scientific papers

Synthesis and biological evaluation of ebselen and its acyclic derivatives

Chang, Tsu-Chung,Huang, Mei-Lan,Hsu, Wen-Lin,Hwang, Jing-Min,Hsu, Ling-Yih

, p. 1413 - 1416 (2007/10/03)

Five ebselen and three acyclic ebselen derivatives were synthesized. These compounds were screened for their glutathione peroxidase (GSH Px)-like activity and scavenging activity against 1,1-diphenyl-2-pycryl-hydrazyl (DPPH) and peroxynitrite radical. All tested compounds displayed similar significant GSH Px-like activity, which are slightly higher than that of ebselen. The peroxynitrite scavenging activity showed that the acyclic allylseleno 4c was five times more potent than ebselen.

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