68230-42-2

Usage

Uses

Used in Organic Synthesis:
(2-METHYL-1-PHENYL-PROPYL)-PHENYL-AMINE is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure allows it to be a versatile component in the synthesis of a wide range of compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2-METHYL-1-PHENYL-PROPYL)-PHENYL-AMINE is used as a key intermediate in the development of new drugs. Its potential chemical and biological properties make it valuable for exploring its efficacy in treating various medical conditions.
Used in Chemical Research:
(2-METHYL-1-PHENYL-PROPYL)-PHENYL-AMINE is also utilized in chemical research to study its properties and interactions with other compounds. This can lead to a better understanding of its potential applications and the development of new methodologies in chemistry.

InChI:InChI=1/C16H19N/c1-13(2)16(14-9-5-3-6-10-14)17-15-11-7-4-8-12-15/h3-13,16-17H,1-2H3

Upstream product

• 38660-83-2 N-(2-methyl-1-phenyl-1-propylidene) aniline 
• 75058-63-8 (E)-N-(2-methyl-1-phenylpropylidene)aniline 
• 62-53-3 aniline 
• 611-70-1 phenyl isopropyl ketone 
• 68230-35-3 3-Methyl-2-phenyl-2-phenylamino-butyronitrile 

Relevant academic research and scientific papers

Chiral Br?nsted Acid-Catalyzed Metal-Free Asymmetric Direct Reductive Amination Using 1-Hydrosilatrane

The asymmetric direct reductive amination of prochiral ketones with aryl amines using 1-hydrosilatrane with a chiral Br?nsted acid catalyst is reported. This is the first known example of chiral Br?nsted acid-catalyzed asymmetric reductive amination using

L-Pipecolinic acid derived Lewis base organocatalyst for asymmetric reduction of N-aryl imines by trichlorosilane: Effects of the side amide group on catalytic performances

A series of N-formamides derived from pipecolinic acid have been synthesized and tested as Lewis base catalysts for the enantioselective reduction of N-aryl imines by trichlorosilane. Through the investigation of the structure-efficacy relationship between the side amide group and catalytic performance, several highly effective catalysts were discovered. In particular, arylamido-type catalyst 5i and non-arylamido-type catalyst 6c exhibited high reactivity and enantioselectivity, furnishing the reduction of a wide variety of N-aryl imines with high isolated yields (up to 98%) and ee values (up to 96%) under mild conditions. Moreover, these two catalysts complement each other in terms of their tolerances to nonaromatic ketimines and non-methyl ketimines. The Royal Society of Chemistry 2013.

L-piperazine-2-carboxylic acid derived N-formamide as a highly enantioselective Lewis basic catalyst for hydrosilylation of N-aryl imines with an unprecedented substrate profile

L-Piperazine-2-carboxylic acid derived N-formamides have been developed as highly enantioselective Lewis basic catalysts for the hydrosilylation of N-aryl imines with trichlorosilane. The arene sulfonyl group on N4 was found to be critical for the high en

Enantioselective synthesis of optically active secondary amines via asymmetric reduction

The enantioselective synthesis of optically active secondary amines via the asymmetric reduction of N-substituted ketimines with various chiral hydride reagents, such as Itsuno's reagent (1), Corey's reagent (2), K glucoride (3), Sharpless' reagent (4), a

Asymmetric Reduction of Schiff's Bases with Lithium Aluminium Hydride-Monosaccharide Complexes to Give Optically Active Secondary Amines

The asymmetric reduction of selected Schiff's bases (ketimines) with the lithium aluminium hydride-monosaccharide complexes derived from 3-O-benzyl-1,2-O-cyclohexylidene-α-D-glucofuranose gives optically active secondary amines.The absolute configuration