57204-41-8

Upstream product

• 636-98-6 p-nitrobenzene iodide 
• 79678-00-5 α-deutero-vinyltrimethylsilane 
• 1193-80-2 α-deuteriostyrene 
• 20455-07-6 p-nitrophenyl methanesulfonate 
• 94781-50-7 α-deuterio-4-nitro-benzaldehyde 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 104960-15-8 1-(p-nitrophenyl)ethyl-1-d tosylate 
• 535995-34-7 C₈H₆⁽²⁾H₂BrNO₂ 
• 619-50-1 4-nitrobenzoic acid methyl ester 
• 104960-14-7 1-(p-nitrophenyl)ethanol-1-d 
• 100-19-6 (4-nitrophenyl)ethanone 
• 73908-63-1 <1-²H₂>-p-nitrobenzyl alcohol 
• 3592-47-0 Benzaldehyde-d 

Relevant academic research and scientific papers

Resolution of the non-steady-state kinetics of the elimination of HBr from 2-(p-nitrophenyl)ethyl bromide in alcohol/alkoxide media

Non-steady-state kinetic studies reveal that the elimination of HBr from 2-(p-nitrophenyl)ethyl bromide in alcohol/alkoxide media, the classical concerted E2 reaction, actually takes place by a two-step mechanism involving the intermediate formation of th

Mechanism of elimination rections. 40. Attempted study of stereochemistry of elimination from 2-(p-nitrophenyl)ethyltrimmethylammonium ion. Base-promoted cis-trans isomerization of p-nitrostyrene-β-d1

Stereospecifically deuterated ArCHDCHDNMe3+I- and ArCHDCHDNMe2O have been prepared, where Ar=C6H5 and p-NO2C6H4.When Ar=C6H5, the elimination reaction of the quaternery salt with ethoxide in ethanol goes with >98percent anti stereoch

On the Electron Impact Induced Hydroxyl Loss from o-Nitrostyrene

Unimolecular hydroxyl (OD.) loss form regio- and stereo-specifically labelled o-nitrostyrenes 1a, 1c and 1d results in the formation of an ion which upon collisional activation gives identical mass spectra.Suggestions are made which aim at explaining: (i) the loss of stereochemical integrity of the diastereotopic methylene hydrogens in the course of hydroxyl elimination; and (ii) to account for the collision induced losses of CO and HCN from the (1+) ion.