100191-85-3

Usage

Uses

Used in Organic Synthesis:
2-(4-Dimethylaminophenyl)furan is used as a building block in organic synthesis for its ability to contribute to the formation of more complex chemical structures. Its unique structure allows for versatile reactions and the creation of a variety of compounds with different properties and applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(4-Dimethylaminophenyl)furan is used as a starting material for the development of new drugs. Its potential biological activity makes it an area of interest for researchers who are exploring its possible therapeutic uses and mechanisms of action.
Used in Chemical Reaction Studies:
2-(4-Dimethylaminophenyl)furan is utilized in the study of chemical reactions to understand its reactivity and the types of products that can be formed. This knowledge is crucial for optimizing synthetic routes and developing new methodologies in organic chemistry.
Used in Medicinal Chemistry:
2-(4-Dimethylaminophenyl)furan is employed in medicinal chemistry as a potential lead compound for the discovery of new pharmaceutical agents. Its structure and properties are investigated to identify how it may interact with biological targets and contribute to therapeutic effects.

Upstream product

• 110-00-9 furan 
• 698-69-1 4-chloro-N,N-dimethylaniline 
• 13331-23-2 fur-2-ylboronic acid 
• 586-77-6 4-bromo-N,N-dimethylaniline 
• 59147-02-3 4-(furan-2-yl)aniline 
• 50-00-0 formaldehyd 
• 6165-76-0 propargyl p-toluenesulfonate 

Relevant academic research and scientific papers

Impact of Five-membered Heterocyclic Rings on Photophysical Properties including Two-photon Absorption Character

A series of dipolar-type terphenyl derivatives 13 featuring an electron donor (p-NMe2C6H4 group) and acceptor (p-NO2C6H4 group) unit was synthesized and their photophysical properties were

Base-Mediated Borylsilylation/Silylation of Ammonium Salts with Silylborane

This work describes a base-mediated borylsilylation of benzylic ammonium salts to synthesize geminal silylboronates bearing benzylic proton under mild reaction conditions. Deaminative silylation of aryl ammonium salts was also achieved in the presence of

Preparation of furans by palladium-catalyzed reaction of acylchromates and propargylic tosylates

Substituted furans are prepared by the palladium-catalyzed reaction of propargylic tosylates with acylchromates. The reaction is initiated by the oxidative additiion of propagylic tosylates to palladium(O) complexes to give 1,2-propadienylpalladium(II) co

Easy photochemical preparation of 2-dimethylaminophenylfurans, -pyrroles and -thiophenes

2-(4-N,N-dimethylaminophenyl) heterocycles are smoothly obtained from the photolysis of 4-chloro-N,N-dimethylaniline in acetonitrile in the presence of furan, pyrrole, thiophene and some of their methyl derivatives bearing a free α-position. With 2,5-dimethyl heterocycles the arylation occurs with equal efficiency in the β position. In the case of furan, when the irradiation is carried out in methanol, cis/trans 2-aryl-5-methoxy-2,5-dihydro adducts are obtained. The reaction is rationalized as involving heterolytic cleavage of the C-Cl bond in the triplet state of the aniline. The intermediacy of the thus formed triplet aryl cation explains the observed high regio- and chemo-selectivity of the process. (C) 2000 Elsevier Science Ltd.