Imines

4-Pyridinedialdoxime is a deuterium-labeled analog of pyridine-2,4-dione. It is a liquid at room temperature and has been shown to have antiviral activity against hepatitis C virus in experimental systems. 4-Pyridinedialdoxime has been shown to inhibit the production of cytokines from human hepatoma cells, which may be due to its ability to inhibit the enzyme ribonucleotide reductase. This chemical can also be used for studies on the equilibrium between the protein and free deuterium. It can be used as an intermediate for synthesizing other compounds, such as 2,6-dioxohexahydropyrimidine.

N,N'-Ethylenebis(trifluoroacetylacetoneimine) is a monoclinic, intramolecular, conjugated, intramolecular hydrogen compound. It has the molecular formula of C8H14F3N3O4 and a molecular weight of 288.8 g/mol. It is also known as ETFAI. This molecule is an organic chemical substance that has an ethane-1,2-dione group with two acetyl groups attached to it. The crystal structure for this molecule is shown in Figure 1 below. Figure 1: Crystal Structure of N,N'-Ethylenebis(Trifluoroacetylacetoneimine)

Applications Salicylaldoxime (cas# 94-67-7) is a useful research chemical.

a-Benzoin oxime is a molecule that has been synthesized and characterized by nuclear magnetic resonance (NMR) spectroscopy. The compound contains a hydroxy group, which is responsible for the vibrational mode observed in anhydrous acetonitrile, sodium citrate and galleria mellonella. This molecule also has a metal ion which coordinates with the hydroxyl group of the benzoin oxime. The coordination complex is formed in an enzyme preparation containing p. aeruginosa and molybdenum as the metal ion.

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(1E)-1-(2,4-Dihydroxyphenyl)ethanone oxime is a selective and catalytic molybdenum-oxo compound that has been shown to be an effective catalyst for the oxidation of anions. The thermal denaturation of this compound has been studied by electrochemical studies. It is insoluble in water and organic solvents. This compound can be used as a ligand in supramolecular chemistry, or it can be cleaved to form dihydroxybenzene derivatives. (1E)-1-(2,4-Dihydroxyphenyl)ethanone oxime is also capable of cleaving naphthalene rings and reacting with alcohols to produce phenols.

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Picolinic acid (PA) is a molecule that is important in the biosynthesis of nicotinamide adenine dinucleotide. This compound can be found in biological samples such as urine, serum, and cerebrospinal fluid. PA has been shown to cause respiratory paralysis at sublethal doses in mice. It has also been shown to have pharmacokinetic properties including significant interactions with other drugs, coordination geometry, nitrogen atoms, intramolecular hydrogen bonding, carboxylate groups, acetylcholine receptors, and sarin gas. PA has been observed to form stable complexes with methochloride and group P2 metals such as copper.

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4-Methylcyclohexanone oxime is an alicyclic compound that has been shown to interact with oxidized, unpaired electrons. The resonance spectra of 4-methylcyclohexanone oxime show a stable, unpaired electron. The spin resonance and resonance spectra of this compound are also stable. Electron spin resonance studies have shown the stereochemical nature of the molecule as well as its unpaired electron. 4-Methylcyclohexanone oxime has been used in organic synthesis for various reactions including ketoxime formation, cyclization, and oxidation reactions.

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