95605-39-3

Basic information

• Product Name: 1-Propanone, 3-(dimethylamino)-1-(3-hydroxyphenyl)-
• CAS NO: 95605-39-3
• Molecular Formula: C11H15NO2
• Molecular Weight: 193.246
• Mol File: 95605-39-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 3-(dimethylamino)-1-(3-hydroxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 3-(dimethylamino)-1-(3-hydroxyphenyl)-(95605-39-3)
• EPA Substance Registry System: 1-Propanone, 3-(dimethylamino)-1-(3-hydroxyphenyl)-(95605-39-3)

Safety Data

• Hazardous Substances Data: 95605-39-3(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 121-71-1 3-Hydroxyacetophenone 
• 506-59-2 N,N-dimethylammonium chloride 
• 5453-62-3 β-dimethylamino-m-hydroxypropiophenone hydrochloride 

Downstream Products

• 76106-47-3 cyclopropyl (3-hydroxyphenyl)methanone 
• 76106-44-0 β-methoxy-m-hydroxypropiophenone 
• 76106-43-9 αβ-epoxy-m-hydroxypropiophenone 
• 76106-42-8 β-dimethylamino-m-hydroxypropiophenone methiodide 
• 76106-45-1 2-[3-(3-Hydroxy-phenyl)-3-oxo-propyl]-malonic acid diethyl ester 

Relevant articles and documents

HCV POLYMERASE INHIBITORS

The invention provides compounds of the formula:wherein B is a nucleobase selected from the groups (a) to (d):and the other variables are as defined in the claims, which are of use in the treatment or prophylaxis of hepatitis C virus infection, and related aspects.

HCV POLYMERASE INHIBITORS

The invention provides compounds of the formula (I) wherein B is a nucleobase selected from the groups (a) to (d): and the other variables are as defined in the claims, which are of use in the treatment or prophylaxis of hepatitis C virus infection, and related aspects.

Intramolecular Alkylation of Phenols. Part 4. Base-catalysed Cyclisation of Phenolic Enones. Scope and Limitations

The phenolic enones (4), (5), (8), (9), and (13) cyclise readily under acidic conditions.However, neither these nor the thio-substituted phenols (11a), (13a), (14a), and (15a) closed under basic conditions.Involvement of unfavourable equilibria is disproved.Comparison is made with related successful cyclisations of the saturated ketone (38) and aldehyde (39).Preliminary results suggest that strict stereo-electronic requirements are necessary for enone ring closure and that these conditions are not met in base-catalysed 5-Endo- and 6-Endo-Trigonal ring closures of the phenols of general type (2; n=0 and n=1).