138888-73-0

Basic information

• Product Name: 1,2-Propanedione, 1-phenyl-, 1-(O-methyloxime)
• CAS NO: 138888-73-0
• Molecular Formula: C10H11NO2
• Molecular Weight: 177.203
• Mol File: 138888-73-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,2-Propanedione, 1-phenyl-, 1-(O-methyloxime)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Propanedione, 1-phenyl-, 1-(O-methyloxime)(138888-73-0)
• EPA Substance Registry System: 1,2-Propanedione, 1-phenyl-, 1-(O-methyloxime)(138888-73-0)

Safety Data

• Hazardous Substances Data: 138888-73-0(Hazardous Substances Data)

Upstream product

• 25355-34-4 1-phenyl-propane-1,2-dione 1-oxime 
• 74-88-4 methyl iodide 
• 77-78-1 dimethyl sulfate 

Relevant articles and documents

The Complex Anionic Rearrangements of Deprotonated α-Oximino Carbonyl Derivatives in the Gas Phase

α-Oximino ketones R1COC(NOH)R2 deprotonate preferentially to form R1COC(NO-)R2 and this anion decomposes by a variety of complex rearrangement processes.The two major fragmentations involve the following overall processes (i) and (ii). (i) R1COC(NO-)R2 R1CO2- + R2CN, and (ii) R1COC(NO-)CH2R -O(R1)C=C=CH2 + RNO (R=H or alkyl).It is proposed that the reaction (i) involves a four-centre reaction of O- at the carbonyl carbon.No evidence of a Beckmann-type rearrangement is indicated for α-oximino ketones.The corresponding deprotonated α-oximino keto ne O-methyl ethers also fragment by complex rearrangement.For example, MeCOC(NOMe)Me deprotonates to form two ions which are interconvertible on collisional activation.The enolate ion is the principial deprotonated species, and it decomposes by the overall process -CH2COC(NOMe)Me --> -CH2CN + CH2CO + MeOH.The other anion decomposes by loss of methanol.This is best rationalised either by the Beckmann process MeCOC(NOMe)CH2- --> -> --> CH2=C=NCOCH2- + MeOH, or a related Neber rearrangement.This investigation was aided by deuterium labelling, and product ion studies.