60940-24-1

Basic information

• Product Name: 2-methylselenobenzanilide
• Synonyms: 2-methylselenobenzanilide
• CAS NO: 60940-24-1
• Molecular Formula: C₁₄H₁₃NOSe
• Molecular Weight: 290.22
• Mol File: 60940-24-1.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 335.4°C at 760 mmHg
• Flash Point: 156.7°C
• Appearance: /
• Vapor Pressure: 0.00012mmHg at 25°C
• CAS DataBase Reference: 2-methylselenobenzanilide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methylselenobenzanilide(60940-24-1)
• EPA Substance Registry System: 2-methylselenobenzanilide(60940-24-1)

Safety Data

• Hazardous Substances Data: 60940-24-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H13NOSe/c1-17-13-10-6-5-9-12(13)14(16)15-11-7-3-2-4-8-11/h2-10H,1H3,(H,15,16)

Upstream product

• 106663-84-7 2,2‘-diselenobis(N-phenylbenzamide) 
• 110-05-4 di-tert-butyl peroxide 
• 93-98-1 N-phenyl benzoyl amide 
• 74-88-4 methyl iodide 
• 1442-04-2 2-methylselenobenzoyl chloride 
• 62-53-3 aniline 
• 60940-34-3 2-phenyl-1,2-benzoisoselenazol-3(2H)-one 

Downstream Products

• 60940-41-2 benzo[d]isoselenazol-3-yl-phenyl-amine 
• 60975-10-2 3-chloro-2-phenyl-benzo[d]isoselenazolium; chloride 

Relevant articles and documents

Horseradish peroxidase inhibition and antioxidant activity of ebselen and related organoselenium compounds

Horseradish peroxidase (HRP) inhibition and glutathione peroxidase (GPx) activities of ebselen and some related derivatives are described. These studies show that ebselen and ebselen ditelluride (EbTe2) with significant antioxidant activity, inhibit the HRP-catalyzed oxidation reactions. In addition, inhibition of lipid peroxidation and singlet oxygen quenching studies were carried out. Although the inhibition of HRP by ebselen is comparable with that of EbTe2, the inhibitory effect on γ-radiation induced lipid peroxidation and the GPx activity of ebselen is found to be much higher than that of EbTe2.

N-phenyl-2-(triphenylstannylseleno)benzamide and 2-methylseleno-N-phenylbenzamide

The two independent molecules of N-phenyl-2-(triphenylstannylseleno)benzamide, C31H25NOSeSn, differ significantly in the conformations of the N-phenylbenzamide groups. For 2-methylseleno-N-phenylbenzamide, C14H13/sub

Expedient Synthesis of Ebselen and Related Compounds

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