6317-69-7

Usage

Uses

Used in Organic Synthesis:
N,N-dimethyl-4-(phenylcarbohydrazonoyl)aniline is utilized as a reagent in organic synthesis, contributing to the formation of various complex organic molecules. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable component in the synthesis of new compounds.
Used in Pharmaceutical Development:
N,N-dimethyl-4-(phenylcarbohydrazonoyl)aniline has been studied for its potential use in the development of new pharmaceuticals. Its specific properties and reactivity may offer advantages in the creation of novel drug candidates, particularly in the areas of medicinal chemistry and drug discovery.
Used in Dye Production:
N,N-dimethyl-4-(phenylcarbohydrazonoyl)aniline also holds potential in the dye industry due to its color-producing characteristics. It can be used as a precursor or intermediate in the production of various dyes, contributing to the development of new colorants for different applications.
Safety and Handling:
It is crucial to handle N,N-dimethyl-4-(phenylcarbohydrazonoyl)aniline with care, as it can be hazardous if not properly managed. The potential health effects of this chemical necessitate adherence to safety guidelines during its use, storage, and disposal to ensure the well-being of individuals and the environment.

InChI:InChI=1/C15H17N3/c1-18(2)14-10-8-13(9-11-14)15(17-16)12-6-4-3-5-7-12/h3-11H,16H2,1-2H3/b17-15+

Upstream product

• 530-44-9 4-(Dimethylamino)benzophenone 

Downstream Products

• 71350-89-5 bis-(4-dimethylamino-benzhydrylidene)-hydrazine 
• 67155-39-9 (p-Dimethylaminophenyl)-phenyldiazomethan 

Relevant academic research and scientific papers

Enantioselective Diarylcarbene Insertion into Si-H Bonds Induced by Electronic Properties of the Carbenes

Catalytic enantioselection usually depends on differences in steric interactions between prochiral substrates and a chiral catalyst. We have discovered a carbene Si-H insertion in which the enantioselectivity depends primarily on the electronic characteristics of the carbene substrate, and the log(er) values are linearly related to Hammett parameters. A new class of chiral tetraphosphate dirhodium catalysts was developed; it shows excellent activity and enantioselectivity for the insertion of diarylcarbenes into the Si-H bond of silanes. Computational and mechanistic studies show how the electronic differences between the two aryls of the carbene lead to differences in energies of the diastereomeric transition states. This study provides a new strategy for asymmetric catalysis exploiting the electronic properties of the substrates.

Cross-Coupling between Difluorocarbene and Carbene-Derived Intermediates Generated from Diazocompounds for the Synthesis of gem-Difluoroolefins

Cross-coupling between difluorocarbene and carbene-derived intermediates generated from diazocompounds was developed to give gem-difluoroolefins, which constitutes a fast practical pathway to achieve hindered gem-difluoroolefins. The cross-coupling between difluorocarbene and aryl diazoacetates proceeded smoothly in the presence of a copper source, whereas its coupling with diaryl diazomethanes occurred well under metal-free conditions. A mechanism involving a copper-difluorocarbene complex was proposed.