41401-03-0

Basic information

• Product Name: Benzeneacetaldehyde, a-phenyl-, oxime
• CAS NO: 41401-03-0
• Molecular Formula: C14H13NO
• Molecular Weight: 211.263
• Mol File: 41401-03-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzeneacetaldehyde, a-phenyl-, oxime(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetaldehyde, a-phenyl-, oxime(41401-03-0)
• EPA Substance Registry System: Benzeneacetaldehyde, a-phenyl-, oxime(41401-03-0)

Safety Data

• Hazardous Substances Data: 41401-03-0(Hazardous Substances Data)

Upstream product

• 530-48-3 1,1-Diphenylethylene 
• 60-29-7 diethyl ether 
• 5670-69-9 1,1'-(2-nitroethene-1,1-diyl)dibenzene 
• 947-91-1 Diphenylacetaldehyde 

Downstream Products

• 451-40-1 phenyl benzyl ketone 
• 1233537-88-6 N-(2,2-diphenylethyl)hydroxylamine 
• 77198-90-4 N-(2,2-diphenylethyl)benzamide 
• 93007-74-0 N-(2,2-diphenylethyl)acetamide 
• 3550-21-8 diphenylmethyl isothiocyanate 
• 4467-90-7 N-hydroxy-2,2-diphenylacetimidoyl chloride 
• 41401-10-9 C₂₈H₂₄N₂O₂ 
• 86-29-3 Diphenylacetonitrile 
• 3963-62-0 2,2-Diphenylethylamine 

Relevant articles and documents

1,2,4-Oxadiazolidin-3,5-diones and 1,3,5-triazin-2,4,6-triones as cytosolic phospholipase A2α inhibitors

1,2,4-Oxadiazolidin-3,5-dione and 1,3,5-triazin-2,4,6-trione scaffolds were employed as templates to incorporate the pharmacophore requirements of cytosolic phospholipase A2α substrate mimetics. Inhibitors that are active in both enzyme, and ce

Titanium(III) Chloride Mediated Reduction of 1-Nitro-2-phenylethenes

The reaction of 1-nitro-2-phenylethenes (β-nitrostyrenes) with aqueous titanium(III) chloride afforded substituted pyrroles in addition to the expected reduction products, oximes and carbonyl compounds. 2-Substituted 1-nitro-2-phenylethenes yielded divinylamine derivatives instead of pyrroles.The reaction mechanism has been rationalized by taking account of the electron transfer from titanium(III) species to the nitro olefines, followed by protonation, dimerization, cyclization, and/or hydrolysis.

TITANIUM TRICHLORIDE MEDIATED REDUCTION OF NITROSTYRENES

Reactions of substituted nitrostyrenes with aqueous titanium trichloride afforded pyrroles, carbonyl compounds, and oximes.In some instances, divinylamines were produced as well.The reaction mechanism is rationalized taking account of electron transfer to nitroethylenes from Ti(III), followed by protonation, dimerization, cyclization, and hydrolysis.