Imines

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1,3-Dichloro-propan-2-one O-benzyl-oxime is a water-soluble compound that falls under the category of research chemicals. It has various applications in the field of chemistry and pharmaceutical research. This compound can be used as a precursor or intermediate in the synthesis of other organic compounds. Its unique chemical structure allows it to react with different functional groups, making it versatile for various reactions and transformations. In addition to its role in research, 1,3-Dichloro-propan-2-one O-benzyl-oxime can also be utilized in industries such as cosmetics, agriculture, and manufacturing. Its solubility in water makes it easy to incorporate into formulations or processes where water-based solutions are required. The compound's compatibility with other substances allows for potential synergistic effects when combined with other active ingredients. Furthermore, 1,3-Dichloro-propan-2-one O-benzyl-oxime has been studied for its

3,4-Dimethylbenzaldehyde oxime is a reactive oxygen species (ROS) that is produced by the oxidation of 3,4-dimethylbenzaldehyde. It has been shown to be an efficient oxidant in aerobic oxidation reactions. The active species generated by this reaction is the aldehyde or ketone form of 3,4-dimethylbenzaldehyde oxime, which can then react with another substrate to generate an oxidized product. This reaction is catalyzed by metal ions and is activated by molecular oxygen.

8-Hydroxyquinoline-2-carbaldehyde oxime is a heteronuclear complex that can be used as a catalyst to produce isonicotinic acid. It is a chelate ligand in which the metal ion binds to one of the two oxygen atoms of the oxime group. The metal ions are coordinated by 8-hydroxyquinoline-2-carbaldehyde oxime, which is coordinated by the metal ions. This coordination results in an increased reactivity of 8-hydroxyquinoline-2-carbaldehyde oxime for the alkali metal cations.

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2-Chlorobenzaldehyde oxime is a compound that inhibits the growth of mycobacterium tuberculosis. It reacts with chloride in the environment to form 2-chlorobenzaldehyde, which reacts with an isoxazole to produce a quinone. Quinones are toxic to mammals and are thought to be responsible for the antimycobacterial activity of this compound. The reaction mechanism of 2-chlorobenzaldehyde oxime has been studied using various techniques and its toxicity has been evaluated in both culture and animal studies. This compound has shown no significant effects on mice at up to 100 mg/kg body weight, but it was found to cause death in rats at doses as low as 0.1 mg/kg body weight. 2-Chlorobenzaldehyde oxime was synthesised by reacting 2-chlorobenzaldehyde with oxalyl chloride under conditions suitable for safety, and the product was purified by recrystallisation from acetone. The synthesis

4-Aminoacetophenone oxime is an organic compound that is soluble in water and methanol. It has a molecular weight of 169.17 g/mol, a melting point of 190 °C, and a boiling point of 260 °C. 4-Aminoacetophenone oxime has been shown to have antimicrobial activity against Gram-positive bacteria, such as Staphylococcus aureus, but not against Gram-negative bacteria. This compound can be used as a ligand for metal ions such as copper and zinc, which are important in biological processes. The magnetic properties of 4-aminoacetophenone oxime make it possible to detect the molecule using nuclear magnetic resonance spectroscopy. 4-Aminoacetophenone oxime can be synthesized by reacting 5-nitrosalicylaldehyde with ammonium acetate in the presence of hydrochloric acid:

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Piperonal oxime is a chemical compound that is used in the synthesis of the fragrance piperonal. It can be produced by the reaction of sodium carbonate and piperonal with an aldehyde such as n-propyl chloride. Piperonal oxime can also be produced by refluxing piperonal in water with sodium carbonate, followed by acidification and polymerization. Piperonal oxime is insoluble in water and has a melting point range between 118-121 °C. The compound has been shown to catalyze the oxidation of benzaldehyde to benzoic acid and o-xylene to ortho-xylene, which are useful for the production of polymers such as nylon 6.

4-(Trifluoromethoxy)Benzamidoxime is a heterocyclic amine compound that is used in the synthesis of hydroxamic acids, hydroxamate, and tetrazole. It has been shown to selectively inhibit MMP-1 over MMP-2, which may be due to its preferentially binding to the active site of MMP-1. 4-(Trifluoromethoxy)Benzamidoxime also inhibits xanthine oxidase and tyrosinase activity. The benzamide isosteres can be synthesized from this molecule by reaction with 3-aminobenzoyl chloride or 3-aminobenzamide.

2-Bromobenzaldoxime is a chemical compound that belongs to the class of isoxazoles. It is used as an agrochemical to control nematodes and insects in crops. 2-Bromobenzaldoxime has been shown to have a high transformation efficiency, with a low response of resistant strains, and is effective against acarids and insects. The product yields are high when 2-bromobenzaldoxime is applied on soil or as a foliar spray. This chemical can be used as an alternative to diethyl ether when it comes to controlling pests in agricultural environments.

2-Oxopropanal oxime is a coordination compound that has been shown to be an effective catalyst for the oxidation of hydrochloric acid to hydrogen chloride and methane. It has also been found to have a protective effect against the nerve agent sarin. 2-Oxopropanal oxime binds to the active site of the enzyme acetylcholinesterase, which breaks down acetylcholine, preventing its action on muscle cells and leading to paralysis. The reaction mechanism of 2-Oxopropanal oxime is not well understood, but it is hypothesized that it may involve a pyridinium intermediate. This compound has been investigated as a possible treatment for metabolic disorders, such as obesity and type II diabetes, due to its ability to stimulate detoxification enzymes in the liver. 2-Oxopropanal oxime is also used in plant biotechnology as an expression plasmid because it allows plants to produce large quantities of proteins with signal pept

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L-Methionine [S]-sulfoximine is a compound that has various applications in research and chemical synthesis. It is commonly used as an inhibitor for certain enzymes involved in the biosynthesis of shikimic acid, which is a precursor for the production of herbicides, aluminum, and boronic compounds. L-Methionine [S]-sulfoximine can also be used as a reagent in the synthesis of pharmaceuticals such as cetirizine and canagliflozin. Additionally, it has been studied for its potential photocatalytic properties and its ability to modulate fibrinogen levels. This versatile compound is highly sought after by researchers and chemists alike for its wide range of applications.

2,6-Dimethylbenzaldehyde oxime is a reagent and useful intermediate for the synthesis of complex compounds. It is also a building block for speciality chemicals. 2,6-Dimethylbenzaldehyde oxime has been used in research and as a reaction component for various organic syntheses. This compound has a CAS number of 55882-62-7.