Chetoni

Applications 1-Cyclohexenyl phenyl ketone is a useful reactant for the synthesis of cyclopentanone enol ethers.
References Huang, X., et al.: J. Am. Chem. Soc., 129, 6398-99 (2007);

(3,5-Dimethoxyphenyl)acetone is a plant phenolic compound that has been found in many plants. It is an intermediate in the biosynthesis of lignans and a wide range of other natural products. The production of (3,5-dimethoxyphenyl)acetone by plants is induced by the presence of nitrate, chloride and/or tyrosol. This compound also represses the expression of genes involved in dextrose metabolism and carbon fixation pathways. Furthermore, it can be quantified using isotopic labelling techniques and has been detected at low levels in human urine samples.

2-Azabicyclo[2.2.1]hept-5-en-3-one is a carbocyclic nucleoside that is synthesized from cyclopentyl and organic solvent, imine, lactam, and fluorine. It has been shown to have potential as a prodrug for the treatment of cancer when it is converted to 2-azabicyclo[2.2.1]heptane by an enzyme called lactamase in the body. Molecular modeling studies show that this compound has a high level of fluidity and can be used in liquid chromatography methods. The enantiomer of this molecule has also been identified and is being studied as a possible drug candidate for the treatment of malaria.

(2,4-Difluorophenyl)acetone is a high quality chemical that can be used as a reagent, intermediate or building block for the synthesis of complex compounds. It is also a versatile building block for the synthesis of speciality chemicals, research chemicals and reaction components. (2,4-Difluorophenyl)acetone is an important intermediate in the synthesis of fluoroquinolones and it has been shown to be useful in the preparation of dyes such as indigo and phthalocyanine. This compound is also used to synthesize other pharmaceuticals such as aspirin and acetaminophen.

1,2-Dihydro-1,5-dimethyl-2-phenyl-3H-pyrazol-3-one (1,2DHDP) is a chemical inhibitor that prevents the activity of enzymes by binding to their active site. 1,2DHDP has been shown to inhibit the enzyme pyrazole ring synthesis in rat liver microsomes. It also inhibits the production of antimicrobial agents and has been used as a sample preparation agent. 1,2DHDP also interferes with drug interactions by inhibiting cytochrome P450 enzymes in the liver. This compound can be used for wastewater treatment because it is not toxic to bacteria or plants. The mechanism of this inhibitor is unknown but may be due to its ability to bind to the dinucleotide phosphate cofactor at the active site of an enzyme.

Please enquire for more information about 2-Ethyl-2-methyl-1,2,3-trihydroquinazolin-4-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Trans-4,5-Dichloro-4,5-dimethyl-1,3-dioxolan-2-one is a fine chemical that can be used as a versatile building block and as an intermediate. It is also useful in research. Trans-4,5-Dichloro-4,5-dimethyl-1,3-dioxolan-2-one has been shown to be a useful reagent in complex organic synthesis because of its high quality. This compound is used to produce useful scaffolds and reaction components.

2,3-Dimethyl-2,5-cyclohexadiene-1,4 dione (DMX) is an antioxidant that has been shown to be effective in the reaction of transfer reactions. DMX has been shown to have a binding constant with fatty acids and is able to inhibit bacterial enzymes such as cytochrome P450s. DMX also reacts with hydroxide solution and forms a salt that can be used as an inhibitor molecule for redox potential. This salt can easily be dissolved in water and is stable at high temperatures. It is possible for DMX to react with molecular modelling software in order to find the optimal reaction conditions for this compound.

1-(4-Amino-3,5-dichloro-phenyl)-2-ethanone is a beta-adrenergic agent. It has been used as a stable isotope label for the study of the pharmacokinetics and metabolism of drugs in humans. In addition, it has been shown to have a good stability profile in acidic solutions and can be easily converted to other derivatives by simple chemical methods. The compound's UV spectrum is linear with respect to concentration over the range from 0.1 to 1 mg/mL, with maxima at 227 nm and 254 nm. This compound has been characterized using analytical methods such as diffraction, spectroscopy, and chromatography.

1,3-Acetonedicarboxylic acid is a crystalline solid that belongs to the group of carboxylic acids. 1,3-Acetonedicarboxylic acid interacts with its receptor by binding to a hydroxyl group and two hydrogen atoms. It has been shown that 1,3-acetonedicarboxylic acid can inhibit HIV infection in vitro by preventing the virus from attaching to cells. It also inhibits malonic acid oxidation and citric acid cycle enzymes in rat liver mitochondria. The synthesis of 1,3-acetonedicarboxylic acid can be achieved through different methods:

1) By reacting sodium carbonate with malonic acid
2) By reacting hydrogen fluoride with malonic acid
3) By reacting sodium carbonate with citric acid (malonic ester) and then hydrolyzing it
4) By reacting sodium carbonate with malonitrile and then hydro

3,3-Dibromopiperidin-2-one is a synthetic reaction product that is used to synthesize diisobutylaluminum. This compound can be found in the sources methylester chloride, pentachloride, thionyl, phosphorus pentachloride, coniferyl alcohol and ferulic acid. It is also an alkaloid compound that has been reported as a palladium catalyst for coupling reactions. 3,3-Dibromopiperidin-2-one is used to synthesize diisobutylaluminum. This compound can be found in the sources methylester chloride, pentachloride, thionyl, phosphorus pentachloride, coniferyl alcohol and ferulic acid. It is also an alkaloid compound that has been reported as a palladium catalyst for coupling reactions.

Heptylphenylketone is a colorless liquid that is soluble in organic solvents. It is used as a chemical intermediate and has been found to be toxic to humans. Heptylphenylketone can be reduced with borohydride, which will result in the formation of phenol. The reduction of heptylphenylketone with borohydride at constant pressure will yield phenol, acetophenone, and benzoic acid. The transport properties of heptylphenylketone are controlled by its hydrophobicity and the degree of hydrogen bonding between the molecules. Human metabolism of heptylphenylketone has been studied by analysis of urine samples collected from volunteers who were given an oral dose of 25 mg/kg body weight. It was found that heptylphenylketone was metabolized mainly by oxidation to produce aldehydes, ketones, acids, fatty acids, and carboxylic acids.

1,3-Dihydroxyacetone is a chemical compound that has been used as a reactant in the synthesis of glycerol. It is the simplest ketone formed from glycerol and a hydroxyl group. The reaction mechanism for the formation of 1,3-dihydroxyacetone involves the reaction of metal hydroxides with glycerol to form an intermediate product, which then reacts with hydrogen peroxide to produce dihydroxyacetone. 1,3-Dihydroxyacetone is also an analytical reagent for phosphorus pentoxide due to its acidic properties. Structural analysis and surface methodology have been used to determine the intramolecular hydrogen bonding between hydroxyl groups on the 1,3-dihydroxyacetone molecule.

4-Propylpyrrolidin-2-one is a chemical compound. It is the product of the condensation of two molecules of butyric acid and one molecule of hexanoic acid. The cyclization reaction occurs at the 4 position, forming a six-membered ring. This reaction can be catalyzed by bromine or UV light. Brivaracetam is a drug that belongs to the class of antiepileptic drugs and was developed as an analog of levetiracetam, which inhibits voltage-gated sodium channels in neurons. It has been shown to have only weak affinity for benzodiazepine binding sites and does not cause sedation or memory impairment.

4-Phenyl-2-butanone is an organic compound that is used as a solvent. It has been shown to be effective against a wide range of bacteria, including Gram positive and Gram negative bacteria. 4-Phenyl-2-butanone disrupts the cell membrane by binding to glycol ether, which is an important part of the lipid bilayer. It also inhibits the synthesis of two important molecules in bacterial cells, dinucleotide phosphate and phospholipids. This process leads to bacterial cell death. 4-Phenyl-2-butanone also has antimicrobial properties due to its ability to destroy water vapor and inhibit growth of microorganisms on skin.

1-(2-Thienyl)-1-butanone (1TBB) is a reactive oxygen species that has been shown to exhibit biological activity. 1TBB is an active oxygen species that can be used as a source of hydrogen peroxide, which is involved in the desulfurization of tobacco and the oxidation of ethylene to produce ethane. 1TBB also reacts with aliphatic aldehydes to form reactive intermediates, which may lead to oxidative injury. 1TBB has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.

(2,6-Difluorophenyl)acetone is an organic compound with the chemical formula CH3C(O)CH=CHF. It is a colorless liquid that boils at 142 °C and has a melting point of about -5 °C. This compound is mainly used as a reagent in organic synthesis, but it can also be used as a building block for complex compounds. The synthesis of (2,6-difluorophenyl)acetone starts by reacting 2-bromo-1,4-phenylene with 2,6-difluoroaniline in benzene. The product can then be purified by distillation or recrystallization to yield high quality (2,6-difluorophenyl)acetone.

Ethyl tridecyl ketone (ETK) is a fatty acid that is an oxidation product of the natural fatty acids found in plants. ETK has been shown to inhibit cell growth and physiological function, which may be due to its ability to react with plasma proteins, such as polysorbate. ETK is also an anti-inflammatory agent and has shown activity against infectious diseases. ETK inhibits the production of inflammatory cytokines by interfering with the synthesis of arachidonic acid, which is an important precursor for these molecules.