52671-42-8

Basic information

• Product Name: 4-nitrosodiphenyl ether
• Synonyms: 4-nitrosodiphenyl ether
• CAS NO: 52671-42-8
• Molecular Formula: C₁₂H₉NO₂
• Molecular Weight: 199.21
• Mol File: 52671-42-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 313.1°Cat760mmHg
• Flash Point: 146.1°C
• Appearance: /
• Density: 1.12g/cm³
• Vapor Pressure: 0.000935mmHg at 25°C
• Refractive Index: 1.568
• CAS DataBase Reference: 4-nitrosodiphenyl ether(CAS DataBase Reference)
• NIST Chemistry Reference: 4-nitrosodiphenyl ether(52671-42-8)
• EPA Substance Registry System: 4-nitrosodiphenyl ether(52671-42-8)

Safety Data

• Hazardous Substances Data: 52671-42-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H9NO2/c14-13-10-6-8-12(9-7-10)15-11-4-2-1-3-5-11/h1-9H

Upstream product

• 620-88-2 4-nitrophenyl phenyl ether 
• 139-59-3 4-phenoxyanilin 
• 3586-12-7 3-phenoxyaniline 
• 51067-38-0 4-phenoxyphenylboronic acid 

Downstream Products

• 104-91-6 p-nitrosophenol 
• 108-95-2 phenol 
• 928206-73-9 8,8-dimethyl-3-(4-phenoxyphenyl)-2-oxa-3-azabicyclo[2.2.2]octan-6-one 
• 928206-74-0 (1R,4R,6R)-8,8-dimethyl-3-(phenoxyphenyl)-2-oxa-3-azabicyclo[2.2.2]octane-6-ol 
• 928206-75-1 benzoic acid 8,8-dimethyl-3-(4-phenoxy-phenyl)-2-oxa-3-aza-bicyclo[2.2.2]oct-6-yl ester 
• 928206-77-3 C₂₈H₂₇NO₅ 
• 928206-76-2 (1R,3R,4R)-3,4-dibenzoyloxy-6,6-dimethyl-1-(4-phenoxyphenylamino)-cyclohexane 
• 1069119-18-1 C₂₂H₂₃NO₇ 
• 1104588-07-9 ((1R,4S)-3-(4-phenoxyphenyl)-2-oxa-3-azabicyclo[2.2.2]oct-5-en-1-yl)methanol 
• 1141700-28-8 C₂₃H₁₉NO₅ 

Relevant articles and documents

Ipso-Nitrosation of arylboronic acids with chlorotrimethylsilane and sodium nitrite

Nitroso compounds are versatile reagents in synthetic organic chemistry. Herein, we disclose a feasible protocol for the ipso-nitrosation of aryl boronic acids using chlorotrimethylsilane-sodium nitrite unison as nitrosation reagent system.

Diastereo- and enantioselective synthesis of nitroso Diels-Alder-type bicycloketones using dienamine: Mechanistic insight into sequential nitroso aldol/Michael reaction and application for optically pure 1-amino-3,4-diol synthesis

This article presents complete diastereo- and highly enantioselective synthesis of nitroso Diels-Alder-type bicycloketones using dienamine. With the hydrogen bonding of two hydroxyls in the bulky binaphthol 1c, high enantioselectivities and complete diast