342423-70-5

Basic information

• Product Name: 1-Hexanone, 1-(3-methoxyphenyl)-
• CAS NO: 342423-70-5
• Molecular Formula: C13H18O2
• Molecular Weight: 206.285
• Mol File: 342423-70-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-Hexanone, 1-(3-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Hexanone, 1-(3-methoxyphenyl)-(342423-70-5)
• EPA Substance Registry System: 1-Hexanone, 1-(3-methoxyphenyl)-(342423-70-5)

Safety Data

• Hazardous Substances Data: 342423-70-5(Hazardous Substances Data)

Upstream product

• 5813-86-5 m-methoxybenzamide 
• 142-61-0 Hexanoyl chloride 
• 100-66-3 methoxybenzene 
• 112545-96-7 1-(hex-1-yn-1-yl)-3-methoxybenzene 
• 62-53-3 aniline 
• 2398-37-0 3-methoxyphenyl bromide 
• 66-25-1 hexanal 

Downstream Products

• 103119-13-7 1-(3-hydroxy-phenyl)-hexan-1-one 
• 157382-25-7 3-Hexyl-phenol 

Relevant articles and documents

Ketide compounds, method for manufacturing, and use for treating diabetes thereof

The present invention relates to ketide compounds, as well as ketide compounds. The present invention relates to a method for preparing a ketide compound, and a use thereof, in which various anti-diabetic TMPA derivative designs can be induced, and is effective in comparison with existing multi-stage synthesis. In addition, the ketide compounds according to the present invention have strong AMPMPK activity and are expected to be useful as a therapeutic agent for diabetes. (by machine translation)

Direct acylation of aryl bromides with aldehydes by palladium catalysis

A new protocol for the direct acylation of aryl bromides with aldehydes is established. It appears to involve palladium-amine cooperative catalysis, affording synthetically important alkyl aryl ketones in moderate to excellent yields in a straightforward manner, and broadening the scope of metal-catalyzed coupling reactions. Copyright

Aquapalladium complex: A stable and convenient catalyst for the intermolecular hydroamination of alkynes

The intermolecular hydroamination of alkynes proceeds very smoothly in the presence of a catalytic amount of the aquapalladium complex [Pd(dppe)(H 2O)2](TfO)2. This reaction most probably proceeds through the formation of an equilibrium between the hydroxopalladium and the amidopalladium complexes, and subsequent aminopalladation of alkynes. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.