101-13-3

Basic information

• Product Name: (3-aminophenyl)-(3-aminophenyl)imino-oxidoazanium
• Synonyms: 3-(3-(3-aminophenyl)-1-oxadiaziridin-2-yl)benzenamine;(3-aminophenyl)-(3-aminophenyl)imino-oxido-ammonium;(3-aminophenyl)-(3-aminophenyl)imino-oxidoazanium;(3-azanylphenyl)-(3-azanylphenyl)imino-oxidanidyl-azanium
• CAS NO: 101-13-3
• Molecular Formula: C₁₂H₁₂N₄O
• Molecular Weight: 228.24988
• Mol File: 101-13-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 507.1°Cat760mmHg
• Flash Point: 260.5°C
• Appearance: /
• Density: 1.3g/cm³
• Vapor Pressure: 2.1E-10mmHg at 25°C
• Refractive Index: 1.657
• CAS DataBase Reference: (3-aminophenyl)-(3-aminophenyl)imino-oxidoazanium(CAS DataBase Reference)
• NIST Chemistry Reference: (3-aminophenyl)-(3-aminophenyl)imino-oxidoazanium(101-13-3)
• EPA Substance Registry System: (3-aminophenyl)-(3-aminophenyl)imino-oxidoazanium(101-13-3)

Safety Data

• Hazardous Substances Data: 101-13-3(Hazardous Substances Data)

Usage

General Description

(3-aminophenyl)-(3-aminophenyl)imino-oxidoazanium is a chemical compound characterized by its complex molecular structure, which consists of two 3-aminophenyl groups linked by an imino-oxidoazanium bridge.

InChI:InChI=1/C12H12N4O/c13-9-3-1-5-11(7-9)15-16(17)12-6-2-4-10(14)8-12/h1-8H,13-14H2/b16-15-

Upstream product

• 50-99-7 D-glucose 
• 99-09-2 3-nitro-aniline 
• 1230-85-9 3,3'-dinitro azoxybenzene 
• 60-29-7 diethyl ether 
• 99-65-0 meta-dinitrobenzene 
• 102-71-6 triethanolamine 
• 111-42-2 2,2'-iminobis[ethanol] 
• 302-01-2 hydrazine 

Downstream Products

• 63494-41-7 bis-(3-acetylamino-phenyl)-diazene-N-oxide 
• 23377-21-1 1,2-bis(3-iodophenyl)diazene 
• 63494-42-8 bis-(3-acetylamino-phenyl)-diazene 
• 19618-17-8 bis-(3-iodo-phenyl)-diazene-N-oxide 
• 108-45-2 m-phenylenediamine 
• 21371-44-8 3,3'-diaminoazobenzene 
• 17540-51-1 3,3'-Azoxy-di-phenol 

Relevant articles and documents

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Palladium Nanoparticles on Silica Nanospheres for Switchable Reductive Coupling of Nitroarenes

Abstract: In this study, we synthesized a robust and sustainable Pd/SiO2 nanospheres catalyst. Further, its catalytic activity was demonstrated for the direct reductive coupling of nitroarenes under mild conditions. While the reaction with Pd nanoparticles on other supporting materials such as modified carbon materials and TiO2, under similar conditions, resulted formation of amines exclusively. Therefore, it was confirmed that the SiO2 was found to be the best supporting material towards the selective reductive coupling of nitroarenes. Also, the catalyst could be recycled up to five cycles with a marginal loss of product yield ( 2% yield). Graphic Abstract: [Figure not available: see fulltext.].