Imines

Please enquire for more information about 6-Methylpyridine-2-carbaldehyde oxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

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(4Z)-3-Methyl-1-phenyl-1H-pyrazole-4,5-dione 4-oxime is a heterocyclic compound. It is a pyrazolone derivative that can be used as coupling agent to form butyl or nitrite esters with basic nitrogenous compounds, such as pyridine or aniline. The compound is also susceptible to nitrosation under acidic conditions and the resulting product is a nitroso compound.

4-Chlorobenzaldehyde oxime is an antibacterial agent that is classified as a chloroamine. It has been shown to be an effective inhibitor of bacterial growth, with a low toxicity to mammalian cells. 4-Chlorobenzaldehyde oxime has been shown to be activated by amines and hydroxylamine, and the resulting intermediate can cleave a variety of bonds in the bacterial cell wall. The molecular orbitals of this compound have been calculated using crystallographic data and functional theory. 4-Chlorobenzaldehyde oxime also binds to chloride ions and forms a complex with ammonium nitrate, which may account for its activity against some bacteria that are resistant to chlorinated compounds (e.g., Clostridium difficile). This compound also contains functional groups that may react with disulfides present in the bacterial cell wall.

Please enquire for more information about 9,10-Dihydro-1-benzo[a]pyrene-7(8H)-one oxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

(S)-(+)-Methyl phenyl sulfoximine, or MMPS, is a synthetic chiral organocatalyst that has been shown to be a highly effective catalyst for the asymmetric synthesis of benzothiazines. It is used in a variety of reactions including cross-coupling, catalytic asymmetric synthesis, desymmetrization and solvents. MMPS has been shown to be enantiopure and stereochemically pure. The yield of this reaction using MMPS as a catalyst was about 98%.

Please enquire for more information about (1E)-1-[3-(2-Morpholin-4-yl-2-oxoethoxy)phenyl]ethanone oxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Phenoxybenzaldehyde oxime is a modified version of 3-phenoxybenzoic acid that inhibits sirtuins. It has been shown to inhibit the activity of SIRT2, which is involved in the regulation of metabolism and aging. The structural modifications on this molecule allow it to bind to the active site of SIRT2 and inhibit its activity. This inhibition leads to decreased cancer cell viability and an inhibitory effect on cancer cells. The pharmacophore for this drug contains lysine residues that are important for binding with SIRT2 and also contains a hydrophobic region that may be important for interactions with other cellular proteins.

3,4-Dichlorobenzaldehyde oxime is a natural carotenoid that has been shown to have antibacterial activity. 3,4-Dichlorobenzaldehyde oxime is produced by the reaction of malonate and aldehyde in an incubated system. This compound has been shown to be active against Gram-positive bacteria such as staphylococcus and aldoximes and Gram-negative bacteria such as E. coli, Salmonella typhimurium, and Shigella flexneri. 3,4-Dichlorobenzaldehyde oxime inhibits bacterial growth by binding to the 50S ribosomal subunit of the bacterial cell membrane. This binding prevents protein synthesis, leading to cell death. The biosynthesis of 3,4-dichlorobenzaldehyde oxime involves the conversion of abscisic acid (ABA) into ABA quinone through oxidation by an enzyme called ABA oxidase

Dimethylglyoxime is a chelate ligand that can be used as an antimicrobial agent. The compound binds to metals, such as iron and copper, which are found in wastewater and industrial effluents. Dimethylglyoxime can also chelate metal ions that are present in the water supply. This property makes it an effective agent for removing heavy metals from water. Dimethylglyoxime has been shown to react with various metal ions by means of Langmuir adsorption isotherms and fluorescence spectrometry. When this reaction occurs, the compound forms a complex with the metal ion. The model system is a solution of dimethylglyoxime with sodium citrate and tetramethylammonium chloride (TMA). The reaction mechanism involves protonation and deprotonation of the ligand, which occurs when the pH is changed from acidic to basic conditions. The plasma mass spectrometry technique has been used to detect the presence of dimethyl

Sipeimine is a natural compound that has been shown to have anti-cancer effects. It is extracted from the roots of peucedanum (fritillaria) and peiminine (peimine). Sipeimine inhibits cancer cell proliferation by blocking DNA synthesis and RNA transcription. It also has hypoglycemic effects. The antitumor activity of sipeimine was first reported in the 1970s, when it was used as an experimental agent for treating leukemia in mice. In recent years, it has been the subject of many research studies because of its potential use in treating chronic cough.

Applications N,N'-Diacetylglyoxime is an intermediates in the synthesis of various nitriles. References Subramanian, L.R., et al.: Sci. Synth., 19, 109 (2004);

2-(Chlorophenyl)methanimine is a fine chemical with CAS No. 91589-24-1 that is used in the synthesis of other research chemicals and speciality chemicals. This compound has a high quality, complex structure, and can be used as an intermediate or scaffold for a variety of reactions. 2-(Chlorophenyl)methanimine is also versatile, as it can be used as a building block or reagent in many different reactions.

4-Iodobenzaldoxime is an isoxazoline, phenyl derivative that forms a 4-iodobenzaldehyde oxime from a 4-bromobenzaldehyde or 4-chlorobenzaldehyde. This compound has been used for the synthesis of organic compounds and pharmaceuticals. The reaction is catalyzed by acid or base in water or alcohol.

Methyltris(methylethylketoxime)silane is a hydrolytic reaction, activated, cross-linking agent that is used in coatings and sealants. It is used in a variety of industrial applications, such as anti-aging, corrosion prevention, and water repellency. Methyltris(methylethylketoxime)silane reacts with calcium carbonate to form a strong bond that is resistant to hydrolysis. This product can be activated by UV irradiation or by adding ammonium persulfate to the solution. The following are some properties of this product: -It has good viscosity -It is an anti-aging agent -It has a hydrolytic reaction -It is an activated cross-linking agent -It has the ability to form coatings and sealants -It can be used for corrosion prevention and water repell

Please enquire for more information about (3Z)-1-(2,6-Dichlorobenzyl)-1H-indole-2,3-dione 3-oxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Acetophenone oxime is a triazine compound that has been shown to inhibit the growth of bacteria by binding to the alcohol group of picolinic acid. The binding of 4-acetophenone oxime to picolinic acid creates an acylation intermediate, which is then hydrolyzed. This reaction is reversible and can be repeated multiple times. The inhibitory effect of 4-acetophenone oxime on bacterial growth is highly dependent on its concentration and the pH of the solution in which it is dissolved. 4-Acetophenone oxime has been used as a reagent for analytical chemistry and as a starting material for other organic compounds such as acetanilide, phenol, and phenylhydrazine. It has also been used in x-ray crystal structures obtained at different temperatures, which provided structural analyses and thermodynamic data.

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2-Methoxyphenyl)acetone oxime is a versatile building block that can be used in the synthesis of complex compounds. It is a colourless crystalline solid with a melting point of 138°C and a boiling point of 188°C. This compound has been assigned CAS No. 43021-97-2 and is soluble in water, ethanol, acetone, benzene, chloroform, ether and ethyl acetate. The chemical structure for this compound is shown below: [[File:2-Methoxyphenyl)acetone oxime.png|thumb|300px|left|The chemical structure for 2-methoxyphenyl)acetone oxime.]]