25725-55-7

Basic information

• Product Name: Ethanone, 1-(4-methoxyphenyl)-2-phenyl-, oxime
• CAS NO: 25725-55-7
• Molecular Formula: C15H15NO2
• Molecular Weight: 241.29
• Mol File: 25725-55-7.mol
• Article Data: 23

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(4-methoxyphenyl)-2-phenyl-, oxime(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(4-methoxyphenyl)-2-phenyl-, oxime(25725-55-7)
• EPA Substance Registry System: Ethanone, 1-(4-methoxyphenyl)-2-phenyl-, oxime(25725-55-7)

Safety Data

• Hazardous Substances Data: 25725-55-7(Hazardous Substances Data)

Upstream product

• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 123-11-5 4-methoxy-benzaldehyde 
• 100-52-7 benzaldehyde 
• 4254-17-5 4-methoxybenzoin 
• 6921-34-2 benzylmagnesium chloride 
• 3424-93-9 4-methoxyphenylacetamide 
• 1023-17-2 4-methoxyphenyl benzyl ketone 
• 5720-07-0 4-methoxyphenylboronic acid 
• 140-29-4 phenylacetonitrile 
• 103-80-0 phenylacetyl chloride 
• 100-66-3 methoxybenzene 

Downstream Products

• 50916-21-7 N-(4-methoxyphenyl)-2-phenylacetamide 
• 1369425-79-5 2-(4-methoxyphenyl)-3-phenylazacyclopropene 
• 13901-72-9 dimethyl 2-(4-methoxyphenyl)-5-phenyl-1H-pyrrole-3,4-dicarboxylate 
• 639524-26-8 3-(4-Methoxy-phenyl)-4-phenyl-5-trifluoromethyl4, 5,-dihydro-isoxazol-5-ol 
• 93913-21-4 threo-1-(4-methoxyphenyl)-2-phenyl-1,2-ethanediamine 
• 93913-22-5 erythro-1-(4-methoxyphenyl)-2-phenyl-1,2-ethanediamine 
• 135147-83-0 erythro-1-(4-hydroxyphenyl)-2-phenyl-1,2-ethanediamine 

Relevant articles and documents

Visible-Light-Promoted [3 + 2] Cycloaddition of 2H-Azirines with Quinones: Access to Substituted Benzo[f]isoindole-4,9-diones

A visible-light-promoteded [3 + 2] cycloaddition reaction of 2H-azirines with quinones has been developed under mild reaction conditions. The reaction provides a general and efficient strategy for the synthesis of the benzo[f]isoindole-4,9-diones scaffold

Photocatalytic Approach for Construction of 5,6-Dihydroimidazo[2,1- A[isoquinolines and Their Luminescent Properties

A visible-light-driven photoredox reaction of tetrahydroisoquinoline with 2H-azirines is described. 4,7-Bis(4-methoxyphenyl)benzo[c][1,2,5]thiadiazole, a benzothiadiazole (BTD) derived fluorophore, is used as an organic photoredox catalyst, and the reacti

A copper-catalyzed insertion of sulfur dioxide: Via radical coupling

A copper-catalyzed three-component reaction of O-acyl oximes, DABCO·(SO2)2, and 2H-azirines under mild conditions has been achieved. This protocol provides an efficient route for the construction of various tetrasubstituted β-sulfonyl N-unprotected enamines in moderate to good yields with excellent stereoselectivity and regioselectivity. Notably, this method represents a rare example of 2H-azirines as useful synthons for β-functionalized N-unprotected enamines. Preliminary mechanistic studies indicate that the reaction proceeds through coupling of a sulfonyl radical and α-carbon radical via copper-catalyzed ring-opening C-C bond cleavage of O-acyl oxime and C-N bond cleavage of 2H-azirine with the insertion of sulfur dioxide.