96746-56-4

Basic information

• Product Name: (E)-β-Methoxy-α-nitrostilbene
• Synonyms: (E)-β-Methoxy-α-nitrostilbene
• CAS NO: 96746-56-4
• Molecular Weight: 255.273
• Mol File: 96746-56-4.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: (E)-β-Methoxy-α-nitrostilbene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-β-Methoxy-α-nitrostilbene(96746-56-4)
• EPA Substance Registry System: (E)-β-Methoxy-α-nitrostilbene(96746-56-4)

Safety Data

• Hazardous Substances Data: 96746-56-4(Hazardous Substances Data)

Upstream product

• 122801-33-6 C₁₈H₁₈NO₅S^(1-) 
• 1215-07-2 (E)-(1-nitroethene-1,2-diyl)dibenzene 
• 876477-04-2 (α'-bromo-α'-nitro-bibenzyl-α-yl)-methyl ether 
• 28925-38-4 α,β-Dinitrostilbene 
• 58593-91-2 α-Iodo-β-nitrostilbene 
• 124-41-4 sodium methylate 
• 159562-65-9 C₁₇H₁₅F₃NO₄^(1-) 
• 162189-76-6 β-(N-methyl-N-methoxyamine)-α-nitrostilbene 
• 122801-32-5 C₁₉H₂₀NO₅S^(1-) 
• 122801-31-4 C₁₇H₁₈NO₄S^(1-) 
• 122801-30-3 C₁₇H₁₈NO₃S^(1-) 
• 253150-02-6 C₁₆H₁₆NO₄^(1-) 
• 67-56-1 methanol 
• 55902-54-0 (E)-1-Iodo-2-nitro-1,2-diphenylethene 

Downstream Products

• 122801-31-4 C₁₇H₁₈NO₄S^(1-) 
• 122801-33-6 C₁₈H₁₈NO₅S^(1-) 
• 122801-32-5 C₁₉H₂₀NO₅S^(1-) 
• 162189-76-6 β-(N-methyl-N-methoxyamine)-α-nitrostilbene 
• 159562-61-5 α-nitro-β-(2,2,2-trifluoroethoxy)stilbene 
• 159562-65-9 C₁₇H₁₅F₃NO₄^(1-) 
• 253150-02-6 C₁₆H₁₆NO₄^(1-) 
• 122801-30-3 C₁₇H₁₈NO₃S^(1-) 
• 73013-91-9 4-((E)-2-Nitro-1,2-diphenyl-vinyl)-morpholine 
• 73013-90-8 1-((E)-2-Nitro-1,2-diphenyl-vinyl)-piperidine 

Relevant articles and documents

The CF3CH2O- adducts of α-nitro-β-(2,2,2-trifluoroethoxy)stilbene and β-methoxy-α-nitrostilbene, and the MeO- adduct of β-methoxy-α-nitrostilbene. Kinetics of competition between protonation and acid catalyzed a

The reaction of aqueous acids with the CF3CH2O- adduct, Ph(OCH2CF3)2CC(Ph)=NO2-, of α-nitro-β-(2,2,2-trifluoroethoxy)stilbene leads virtually exclusively to the corres

Kinetic analysis of elementary steps in nucleophilic vinylic substitution reactions of α-nitro-β-X-stilbenes (X = OCH2CF3, OCH3, NO2) with various nucleophiles.

Rate constants of elementary steps in the addition-elimination mechanism of nucleophilic vinylic substitutions (SNV) were determined by studying the following reactions in 50% Me2SO-50% water at 20 °C: (1) α-nitro-β-(2,2,2-trifluoroethoxy)stilb

Kinetics of reactions of hydroxide ion and water with β-X-substituted α-nitrostilbenes (X = Cl, I, SEt, OMe, SCH2CH2OH) in 50% Me2SO-50% water. Search for the intermediate in nucleophilic vinylic substitution

The hydrolysis of Ph(LG)C=Cph(NO2) (4-LG, Lg = Cl, I, Set, Ome) in basic solution yields the anion of 1,2-diphenyl-2-nitroethanone, PhC(=O)C(=NO2-)Ph (8-), by the addition-elimanation mechanism of nucleophilic v