5809-25-6

Usage

Uses

Used in Organic Synthesis:
(4-aminophenyl)[4-(dimethylamino)phenyl]methanone is used as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its presence of both amino and dimethylamino groups allows for a wide range of chemical reactions, making it a valuable component in the synthesis of new compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (4-aminophenyl)[4-(dimethylamino)phenyl]methanone is used as a building block in the development of new drugs. Its unique structure and functional groups contribute to the design and synthesis of potential therapeutic agents, aiding researchers in their quest to discover innovative medications.
Used in Material Development:
(4-aminophenyl)[4-(dimethylamino)phenyl]methanone also finds application in the development of new materials. Its chemical properties and reactivity make it suitable for creating novel materials with specific properties for various industrial applications.
It is important to handle (4-aminophenyl)[4-(dimethylamino)phenyl]methanone with care due to its potential health hazards if not properly managed.

Upstream product

• 90-94-8 bis(p-dimethylaminophenyl)methanone 
• 548-62-9 crystal violet 
• 1217306-78-9 tert-butyl 4-[4'-(dimethylamino)benzoyl] phenylcarbamate 
• 1226-45-5 (4-(dimethylamino)phenyl)(4-nitrophenyl)methanone 
• 569-64-2 Malachitgruen 

Relevant academic research and scientific papers

A series of BiO: XIy/GO photocatalysts: Synthesis, characterization, activity, and mechanism

A series of bismuth oxyiodide (BiOxIy)-grafted graphene oxide (GO) sheets with different GO contents were synthesized through a simple hydrothermal method. This is the first report where four composites of BiOI/GO, Bi4O5I2/GO, Bi7O9I3/GO, and Bi5O7I/GO have been characterized using X-ray diffraction, transmission electron microscopy, scanning electron microscopy energy-dispersive spectroscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and diffuse reflectance spectroscopy. The assembled BiOxIy/GO composites exhibited excellent photocatalytic activities in the degradation of crystal violet (CV) under visible light irradiation. The order of rate constants was as follows: Bi7O9I3/GO > Bi4O5I2/GO > Bi4O5I2 > Bi7O9I3 > Bi5O7I/GO > BiOI/GO > BiOI > Bi5O7I > GO. The photocatalytic activity of the Bi7O9I3/GO (or Bi4O5I2/GO) composite reached a maximum rate constant of 0.351 (or 0.322) h-1, which was 1.8 (or 1.7) times higher than that of Bi7O9I3 (or Bi4O5I2), 6-7 times higher than that of BiOI/GO, and 119-130 times higher than that of BiOI. The quenching effects of different scavengers and electron paramagnetic resonance demonstrated that the superoxide radical (O2-) played a major role and holes (h+) and hydroxyl radicals (OH) played a minor role as active species in the degradation of crystal violet (CV) and salicylic acid (SA). Possible photodegradation mechanisms are proposed and discussed in this research.

SURFACE ENHANCED RAMAN SPECTROSCOPY (SERS) COMPOUNDS AND METHODS OF THEIR PREPARATION

A compound for detecting an analyte using Surface Enhanced Raman Spectroscopy (SERS) and a method of forming the compound is provided. The compound has Formula I: wherein W is selected from the group consisting of an optionally substituted aryl group and an optionally substituted heteroaryl group; each Y independently is NR1R2, wherein R1 and R2 are independently selected from the group consisting of H and C1-C6 alkyl, or R1 and R2 combine to form together with the nitrogen to which they are attached a heterocyclic group with 4 to 5 carbon atoms, is used to denote a single or a double bond, and Z is NH, NH2, NH—(C═O)—(CH2)n—SH, wherein n=1 to 10, or or a tautomer or stereoisomer thereof, or a salt thereof. A method and device for detecting an analyte using Surface Enhanced Raman Spectroscopy (SERS) is also provided.

Combinatorial synthesis of a triphenylmethine library and their application in the development of Surface Enhanced Raman Scattering (SERS) probes

The first synthesis of a triphenylmethine (TM) library of compounds and screening of their Surface Enhanced Raman Scattering (SERS) capability was carried out to identify novel Raman reporters with high sensitivity. We identified three novel SERS reporters (B2, B7, and C7) with higher signal intensity than that of commonly used crystal violet (CV). These reporters may find potential applications in developing sensitive SERS based biosensors.

Photocatalytic degradation of michler's ketone in water by Uv light illumination using TiO2 photocatalyst: Identification of intermediates and the reaction pathway

The TiO2/UV photocatalytic degradation ofMichler's Ketone (MK) has been investigated in aqueous heterogeneous suspensions. Results obtained show rapid and complete oxidation of MK after 24-h, and more than 97.5% of MK was mineralized after a 32-h exposure

Urea thiadiazole inhibitors of plasminogen activator inhibior-1

Methods of treating disorders associated with elevated levels of PAI-1 are disclosed comprising administering to a patient in need thereof a therapeutically effective amount of at least one compound of formula (I), or a pharmaceutically-acceptable salt, prodrug, stereoisomer or solvate thereof, wherein: A is aryl o heteroaryl, and R1-R12, are defined herein. The invention also pertains to pharmaceutical compositions and compounds within the scope of formula (I) as well as medicaments and articles of manufacture comprising compounds of formula (I).

Photo-Fenton degradation of malachite green catalyzed by aromatic compounds under visible light irradiation

The photo-Fenton degradation of malachite green (MG) catalyzed by aromatic derivatives under visible light irradiation was examined. Aromatic derivatives exhibit significant catalytic action in the photo-Fenton reaction. The degradation rates of MG with various kinds of aromatic derivatives obey the following order: hydroquinone > salicylic acid > quinone > carboxylic aromatic derivatives > amido aromatic derivatives. GC-MS detection of the products formed in the MG Fenton degradation in the presence of aromatic derivatives shows that the addition of the latter does not change the MG degradation pathways, although it greatly alters the reaction rate. The MG degradation mainly involves two different pathways: cleavage with a [MG-OH]· transition intermediate and N-demethylation.