113598-55-3

Usage

Chemical Category

The compound belongs to the category of ketones.

Usage in Fragrances and Flavorings

The compound is commonly used in the production of fragrances and flavorings due to its pleasant aroma.

Application in Pharmaceutical Industry

The compound is used as an intermediate in the synthesis of various drugs and pharmaceutical products.

Use in Manufacturing Polymers

The compound has applications in the manufacture of polymers and other organic compounds.

Upstream product

• 113598-57-5 N-(2,2-dimethyl-3-phenyl-1-p-tolylpropylidene)methylamine 
• 401636-52-0 di-tert-butyl 4-benzyl-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate 
• 14289-68-0 2-bromo-2-methyl-1-(4-methylphenyl)-1-propanone 
• 122-78-1 phenylacetaldehyde 
• 73305-96-1 N-(3-amino-2-methyl-1-phenyl-3-p-tolyl-allylidene)-4-methyl-aniline 
• 74-88-4 methyl iodide 
• 138356-05-5 3-imino-1,N-diphenyl-2-methyl-3-(p-tolyl)prop-1-enylamine 

Relevant academic research and scientific papers

Building Congested Ketone: Substituted Hantzsch Ester and Nitrile as Alkylation Reagents in Photoredox Catalysis

For the first time, 4-alkyl Hantzsch esters were used to construct molecules with all-carbon quaternary centers by visible light-induced photoredox catalysis via transfer alkylation. Up to a 1500 h-1 turnover frequency was achieved in this reaction. Reactions of 4-alkyl Hantzsch nitriles as tertiary radical donors joined two contiguous all-carbon quaternary centers intermolecularly, and this chemistry was used to synthesize a common precursor of a class of hydroxysteroid dehydrogenase inhibitors.

Reaction of 3-Amino-2-alkenimines with Alkali Metals: Unexpected Synthesis of Substituted 4-(Arylamino)quinolines

A study of the reduction of 3-amino-2-alkenimines 1 with alkali metals is reported.The nature of the alkali metal plays an important role in the course of the process.In this context, a new and simple method for the regioselective synthesis of 4-(arylamino)quinolines 4 from 1 and sodium or potassium is described.

Mild and Regiospecific Reduction of Masked 1,3-Dicarbonyl Derivatives to Monocarbonyl Compounds and Primary and Secodary Amines

The regiospecific reduction of masked 1,3-dicarbonyl compounds to the corresponding saturated monocarbonyl 3 or iminic 4 compounds via 3-amino-2-alkenimines 1 is described.The formation of 3 and 4 can be explained in terms of a double reduction process from 1.A simple method for the synthesis of primary and secondary amines 6 is also described.