61053-50-7

Basic information

• Product Name: Benzene, 1-(methylseleno)-2-nitro-
• CAS NO: 61053-50-7
• Molecular Formula: C7H7NO2Se
• Molecular Weight: 216.098
• Mol File: 61053-50-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(methylseleno)-2-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(methylseleno)-2-nitro-(61053-50-7)
• EPA Substance Registry System: Benzene, 1-(methylseleno)-2-nitro-(61053-50-7)

Safety Data

• Hazardous Substances Data: 61053-50-7(Hazardous Substances Data)

Upstream product

• 5570-19-4 2-nitrophenylboronic acid 
• 7101-31-7 dimethyl diselenide 
• 552-16-9 ortho-nitrobenzoic acid 
• 1493-27-2 ortho-nitrofluorobenzene 
• 365-33-3 2-nitrobenzenediazonium tetrafluoroborate 

Downstream Products

• 1265625-23-7 C₃₂H₃₀N₆OSe 
• 1265625-21-5 C₅₁H₄₄N₆OSe 
• 1265625-27-1 2-butyl-1-(4-carboxybenzyl)-5-[2-carboxy-3-(benzo[b]selenophen-1-yl)prop-1-enyl]-1H-imidazole 
• 27350-33-0 2-phenylbenzo[b]selenophene 
• 89723-13-7 benzo[d][1,3]selenazol-2-yl(phenyl)methanone 
• 89723-06-8 N-(2-(methylselanyl)phenyl)acetamide 
• 32586-68-8 2-phenylbenzo[d][1,3]selenazole 
• 2818-88-4 2-methylbenzoselenazole 
• 273-91-6 benzoselenazole 
• 70086-67-8 2-(methylselanyl)aniline 
• 1657-95-0 2.4.2'-Trinitro-diphenylselenid 

Relevant articles and documents

Structure and spectroelectrochemical response of arene-ruthenium and arene-osmium complexes with potentially hemilabile noninnocent ligands

Nine of the compounds [M(L2-)(p-cymene)] (M = Ru, Os, L2- = 4,6-di-tert-butyl-N-aryl-o-amidophenolate) were prepared and structurally characterized (Ru complexes) as coordinatively unsatu-rated, formally 16 valence electron species.

Synthetic method of aryl methyl selenide compound

The invention relates to a synthetic method of an aryl methyl selenide compound. In an organic solvent, under the oxygen condition, aryl carboxylic acid and dimethyldiselenide are used as reaction raw materials to obtain the aryl methyl selenide compound through oxidative decarboxylation coupling reaction under the joint promoting effect of a copper catalyst, a ligand and alkaline. The aryl carboxylic acid and the copper catalyst adopted in the method are cheap and easy to obtain, a substance range is wide, the reaction condition is simple, the product yield and purity are high, a new synthetic route and method is developed for the aryl methyl selenide compound, and the aryl methyl selenide compound has good utilization potential and a research value.

Tandem free-radical addition/substitution chemistry and its application to the preparation of novel AT1 receptor antagonists

Benzothiophene and benzoselenophene analogues of the thiophene-containing antihypertensives milfasartan and eprosartan were prepared and tested for AT1 receptor antagonist properties. While the sulfur-containing systems were prepared following