55439-08-2

Basic information

• Product Name: 3-Hydroxy-2-methyl-1-oxo-1-phenylprop-2-ene
• Synonyms: 3-Hydroxy-2-methyl-1-oxo-1-phenylprop-2-ene
• CAS NO: 55439-08-2
• Molecular Weight: 162.188
• Mol File: 55439-08-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-Hydroxy-2-methyl-1-oxo-1-phenylprop-2-ene(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Hydroxy-2-methyl-1-oxo-1-phenylprop-2-ene(55439-08-2)
• EPA Substance Registry System: 3-Hydroxy-2-methyl-1-oxo-1-phenylprop-2-ene(55439-08-2)

Safety Data

• Hazardous Substances Data: 55439-08-2(Hazardous Substances Data)

Upstream product

• 105787-50-6 4,4'-<3,3'-Oxybis(2-methyl-1-phenyl-2-propenyliden)>dimorpholinium-bis(trifluormethansulfonat) 

Downstream Products

• 87294-83-5 (Z) 3,5-Diphenyl-2-methylhexa-2,5-dienal 
• 87294-84-6 (E) 3,5-Diphenyl-2-methylhexa-2,5-dienal 
• 344261-34-3 6-methyl-5-phenyl-1,2,3,4-tetrahydro-1,8-naphthyridine 
• 77871-79-5 3-methyl-4-phenyl-1,2,3,4-tetrahydro-1,6-naphthyridine 
• 77871-77-3 3-methyl-4-phenyl-1,2,3,4-tetrahydro-1,8-naphthyridine 
• 77871-78-4 3-methyl-4-phenyl-1,2,3,4-tetrahydro-1,5-naphthyridine 
• 77871-82-0 3-Methyl-4-phenyl-[1,6]naphthyridine 
• 77871-80-8 3-Methyl-4-phenyl-[1,8]naphthyridine 
• 77871-81-9 3-Methyl-4-phenyl-[1,5]naphthyridine 
• 72945-07-4 2-Methyl-1-phenyl-3-(4'-pyridylamino)propan-1-ol 
• 72945-06-3 2-Methyl-1-phenyl-3-(3'-pyridylamino)propan-1-ol 
• 72945-05-2 2-Methyl-1-phenyl-3-(2'-pyridylamino)propan-1-ol 
• 22582-40-7 5-methyl-6-phenyl-(2H)-pyran-2-one 
• 125748-71-2 (Z)-2-Methyl-1-phenyl-3-trimethylsilanyloxy-propenone 

Relevant articles and documents

Dication Ethers, 12. - Reaction of Enaminones with Triflic Anhydride: 3-Trifloxypropeniminium- and Bis(3-amino-2-propenylio) Ether Salts

Reaction of enaminones 1 a-n with triflic anhydride (Tf2O) in a 1:1 molar ratio yields 3-trifloxypropeniminium triflates 2 a-n by O-sulfonylation.With a 2:1 molar ratio, the bis(3-amino-2-propenylio) ether bistriflates 3 are obtained.The configuration of the cations of 2 and 3 is derived from 1H and 13C NMR data as far as possible.Hydrolysis of the ambifunctional salts 3 may occur either at the iminium or the vinyl ether functions.