Imines

Applications Dimethylglyoxime is a chelating agent which forms complexes with metals such as copper, nickel, and palladium.. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

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Applications Benzamide Oxime is used to prepare aryloxadiazoles as apoptosis inducers and anticancer agents. It is also used in the synthesis of aryloxadiazolyltropane analogs of cocaine. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Zhang, H., et al.: J. Med. Chem., 48, 5215 (2005); Carroll, F., et al.: J. Med. Chem., 36, 2886 (1993)

Applications Dibromoformaldoxime is a reagent that undergoes cycloaddition with alkynes to prepare substituted 3-bromo-isoxazoles in high yield. References Chiarino, D., et al.: J. Heterocyclic Chem., 24, 43 (1987); De Amici, M., et al.: J. Org. Chem., 54, 2646 (1989); Castelhano, A., et al.: 16, 335 (1988).

3-Bromobenzaldoxime is a dialkylamino aldoxime compound that is soluble in organic solvents such as diethyl ether, chloroform, dichloromethane, and benzene. It can be synthesized from benzaldehyde and aniline through the reaction of cyclopentenes with phenylsulfonyl chloride. This reaction produces an intermediate that is then reacted with nitrobenzene to produce 3-bromobenzaldoxime. 3-Bromobenzaldoxime has been used in the synthesis of hydroxamic acids and its use as a solvent for nitro compounds.

alpha,4-Dichlorobenzaldoxime is a synthetic ligand that inhibits bacterial DNA replication. It has been shown to inhibit the growth of staphylococcus and streptococcus by binding to their nucleic acids and preventing transcription. alpha,4-Dichlorobenzaldoxime may have anticancer potential and could be useful in chemotherapy treatments for some types of cancer. The mechanism of action is thought to be due to its ability to react with an amine group on an amino acid or protein, forming a hydroxyamine intermediate which can react with another amine group on another molecule. This reaction leads to the formation of a new chemical bond between the two molecules and prevents the production of proteins vital for cell division.

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4-(N,N-Dimethylamino)benzaldoxime is an efficient method for the detection of cinnamic acid and its esters. It reacts with aldehydes to form 4-nitrosobenzaldehyde products that are detectable by ultraviolet spectroscopy. The reaction takes place in aqueous solutions with a pH range of 5-8 and is catalyzed by an enzyme called carboxylate. This reaction has been shown to be useful for the detection of cinnamic acid and its esters in food, tobacco smoke, and other samples.

Applications Acetaldoxime is a useful research chemical, an intermediate or a precursor used in the preparation of some heterocyclic compounds like spiroisoxazolines. An oxygen scavenger in boiler water. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Lee, C. K. Y., et al.: ARKIVOC, 3, 175 (2006); Gallos, J. K., et al.: J. Chem. Soc., 4, 415 (2001); Zhao, Z., et al.: From Faming Zhuanli Shenqing (2019), CN 109368821 A 20190222

D,L-Buthionine-(S,R)-sulfoximine is a basic compound with a sulfur atom. It has been shown to have antioxidative properties. D,L-Buthionine-(S,R)-sulfoximine can be used in the treatment of infectious diseases caused by bacteria or viruses that are sensitive to oxidative injury. It also has inhibitory properties against toll-like receptor 4 (TLR4), which may be useful for treating inflammatory bowel disease. D,L-Buthionine-(S,R)-sulfoximine can also be used as an anti-inflammatory agent and an antioxidant in eye disorders. This compound can be used in the treatment of radiation injuries and eye disorders due to its ability to inhibit cell nuclei from dying by preventing DNA fragmentation.

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2,6-Dimethoxybenzaldoxime is a phenylhydrazone that can be used in the catalytic system for oxidation of carbonyl compounds. The reaction proceeds through the periodate-mediated oxidation of the hydrazone to form the corresponding hydroxamic acid. This compound has been shown to be efficient and selective for the oxidation of a wide range of carbonyl compounds, including porphyrins. 2,6-Dimethoxybenzaldoxime is also used as a precursor for other syntheses, such as tetraphenylporphyrin.

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L-Methionine [R]-sulfoximine is a molecule that has been isolated from the environment. It is an electron-deconvolution and paramagnetic resonance study of the molecule. The spectrum was obtained in the frequency range from 10 to 500 MHz, with a resolution of 0.03 ppm, and a sensitivity of 20 μT. L-Methionine [R]-sulfoximine is an imine nitrogen that can be coordinated by metal ions to form an iminium ion. This compound has two enantiomers, which are both shown in this study. L-Methionine [R]-sulfoximine is a synthetase that catalyzes the formation of the methylamino group and its amino nitrogen.

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Obidoxime chloride is an analytical reagent that is used to measure aminotransferase activity, a process in which amino acids are broken down into other substances. Obidoxime chloride is also used in the pharmaceutical industry as a solvent and as a preservative. It has been found to have anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis. The biological properties of obidoxime chloride are related to its ability to bind with nitrogen atoms and inhibit the production of inflammatory compounds such as il-2 receptor and symptoms.

Acetaldoxime is a chemical compound that is used as a fast-acting antidote for poisoning by organophosphate nerve agents. Acetaldoxime binds to the phosphorylcholine of the enzyme acetylcholinesterase, preventing the breakdown of acetylcholine and relieving muscle paralysis. Acetaldoxime can be used in biological treatment processes to remove nitrogenous wastes from wastewater, such as methyl ethyls or hydroxyl groups. It has been shown that acetaldoxime reacts with sodium carbonate to form stable complexes, which are characterized by their kinetic energy and reaction mechanism. Acetaldoxime also participates in physiological functions such as the synthesis of fatty acids and cholesterol, which are important for maintaining cell membrane integrity.

Applications (E)-1-(Benzo[b]​thiophen-​2-​yl)ethanone Oxime is an isomer of N-​(1-​Benzo[b]​thiophen-​2-​yl-​ethyl)​-​hydroxylamine a reagent used in the preparation of Zileuton, an anti-asthmatic drug. References Guinchard, X. et al.: J. Org. Chem., 73, 2028 (2008)

Nicotinaldehyde oxime is a polyimide with nicotinic acetylcholine as the monomer unit. It is synthesized by a supramolecular process and has an oxime group in its molecular structure. This product has been shown to have antioxidant and anticholinergic properties, which may be due to its ability to form hydrogen bonds with other compounds. Nicotinaldehyde oxime is used in industrial applications such as the manufacture of optical components, horticultural applications, or transfer reactions.

Bis(1H-benzo[d][1,2,3]triazol-1-yl)methanimine is a ligand that reacts with chloride ions to form the corresponding bis-(chloroformate) and a carboxylic acid. It can be used as an intermediate in organic synthesis reactions involving chlorides. Bis(1H-benzo[d][1,2,3]triazol-1-yl)methanimine hydrolyzes to benzotriazole and acetate when treated with water or acidic conditions.

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Syringaldoxime is a tyrosinase inhibitor that inhibits the production of melanin. It is used in the treatment of vitiligo, a skin condition characterized by patches of depigmented skin. Syringaldoxime binds to benzal-dioxime and inhibits its activity. This inhibition leads to decreased production of hydroxytyrosine, which is an important intermediate in the synthesis of melanin. It also has inhibitory activity against l-dopa oxidation and enzyme catalyzed reactions. Syringaldoxime has two moieties, tropolone and methoxy, which are responsible for its inhibitory effects on tyrosinase activity.

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Cyclohexanone oxime is a toxic substance that has been shown to be an inhibitor of the reaction mechanism. Cyclohexanone oxime is a solid catalyst that can be used for electrochemical studies and to study the reaction kinetics. The molecule has two reactive groups: a hydroxyl group and trifluoroacetic acid, which are both acidic. Cyclohexanone oxime has a coordination geometry with one metal atom (zinc) and one ligand (cyclohexanone).

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Applications (E)-1-(2,6-Dimethylphenoxy)propan-2-one oxime is a useful reagent for organic synthesis.

Deoxybenzoic oxime is an oxime derivative that inhibits the enzyme toll-like receptor 4 (TLR4) and also blocks activation of chloride channels. It has been shown to inhibit the production of nitric oxide and proinflammatory cytokines in vitro. Deoxybenzoic oxime has also been shown to have a broad spectrum of activity against chemical species, such as benzonitrile, sulfide, and amines. This drug has shown inhibitory activities against a wide variety of functional groups including hydroxyl, nitrile, amine, thiol, ethers, phosphates and carboxylic acids.

Benzamidoxime is a water-soluble organometallic compound that has a basic structure. The benzimidazole ring has two C-H bonds, one of which is adjacent to the nitrogen atom in the diphenyl ether ring. This compound can be found as a salt or an acid and it may also be used as a catalyst for organic reactions. Benzamidoxime is typically prepared by reacting sodium carbonate with an organic halide and hydrochloric acid, or alternatively by reacting sodium carbonate with hydrogen chloride gas. It is also possible to prepare this compound by reacting benzene with ammonia and formaldehyde at elevated temperatures and pressures. This compound can be used in wastewater treatment due to its ability to bind metal ions, such as copper, mercury, zinc, lead, nickel and chromium. It also has been shown to have anti-inflammatory properties in human liver cells because of its binding affinity for nucleotides containing dinucleotide phosphate groups.

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N-Acetyl-4-benzoquinone imine is an antimicrobial agent that belongs to the class of paracetamol. It inhibits the enzyme form of acetaminophen (APAP). N-Acetyl-4-benzoquinone imine is a reactive compound and can cause oxidative injury in cells. This drug has been shown to have cytotoxic effects on cells at physiological levels and a concentration-time curve similar to acetaminophen. N-Acetyl-4-benzoquinone imine also affects mitochondrial membrane potential and matrix effect, which may be due to its ability to inhibit mitochondrial enzymes. The toxic effects of N-Acetyl-4-benzoquinone imine are reversible after it is metabolized by cytochrome P450 enzymes.

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Pivalaldehyde oxime is a reactive compound that forms through the nucleophilic attack of carboxylic acid anhydrides on alcohols. Pivalaldehyde oxime reacts with metal ions to form metal carboxylates, which are useful reagents in analytical chemistry. This compound also has nitro groups that are sensitive to oxidizing agents and can be used as an indicator for the presence of oxygen in organic compounds. Pivalaldehyde oxime can cause cell apoptosis, which may be due to its ability to induce DNA fragmentation and mitochondrial dysfunction. It is found in environmental pollution and can be used agriculturally as a synergist for amines.

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2,3-Dichlorobenzaldehyde oxime is a versatile building block and reagent in the synthesis of complex compounds. It is mainly used as a research chemical and speciality chemical. 2,3-Dichlorobenzaldehyde oxime has been widely used for the preparation of fine chemicals, pharmaceuticals, agrochemicals, and other organic compounds. This compound can be reacted with various reagents to produce useful scaffolds or reaction components.

4-Benzoquinone monoxime (BQM) is a phospholipid analog that has reactive properties. It reacts with hydrochloric acid to form a nitrite ion, which is then reduced to nitric oxide. Nitric oxide has been shown to be effective in the treatment of bacterial infections and as a disinfectant. BQM also reacts with hydroxyl groups, producing sephadex g-100, which is used for separation of biological materials. The reaction mechanism of BQM has been studied using deuterium isotope labeling and electrochemical detection. This reaction takes place on the cytosolic surface of bacteria and on protein synthesis enzymes in the cytoplasm.

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alpha-Chloro-3-nitrobenzaldoxime is an antimicrobial agent that belongs to the group of itraconazole. It is a synthetic compound that was synthesised for its anti-fungal properties. alpha-Chloro-3-nitrobenzaldoxime has been shown to be effective against candida albicans and other fungi, which may be due to its ability to inhibit the production of 1,3-dipolar cycloaddition products from aldehydes. alpha-Chloro-3-nitrobenzaldoxime also inhibits the synthesis of proteins and RNA by inhibiting protein synthesis at the ribosome level. This drug can be used in conjunction with fluconazole for more efficient antifungal activity.

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Benzenesulphonyl)acetamide oxime is a herbicide that inhibits the growth of plants by binding to the enzyme acetohydroxy acid synthase, which is involved in the synthesis of fatty acids. The compound has been shown to be a potent herbicide against many types of weeds, such as thistles, canary grass, ragweed, and lambsquarters. Benzenesulphonyl)acetamide oxime is also used as an analytical reagent to detect peroxides.

Applications An antioxidant References Jeong, H., et al.: Bioorg. Med. Chem. Lett., 16, 5576 (2006), Andresen Bergstroem, M., et al.: J. Med. Chem., 51, 2541 (2008),

3,4,5-Trimethoxybenzaldehyde oxime is a synthetic heterocyclic compound that belongs to the group of isoxazoles. It has been shown to have anti-cancer properties in vitro and in vivo by inhibiting the growth of human breast cancer cells. 3,4,5-Trimethoxybenzaldehyde oxime also inhibits the production of 5-hydroxytryptamine (serotonin) and chloride ions in t47d cells. This compound has been shown to be an isomeric mixture of syn and anti forms. The syn form has a higher affinity for the 5-ht receptor than the anti form does.

Bropirimine is a drug that acts as an anti-cancer agent and has been used in the treatment of autoimmune diseases. It inhibits the growth of cancer cells by binding to basic proteins, which are involved in intermolecular hydrogen bonding, and inducing apoptosis. Bropirimine also binds to toll-like receptor 4 (TLR4) and inhibits the production of inflammatory cytokines by macrophages, thereby inhibiting inflammation. Bropirimine also has metabolic effects, such as reducing blood sugar levels and improving insulin sensitivity in animal models with high blood sugar levels. The molecular pathogenesis of bropirimine is not well understood, but it may involve hydrogen bonding interactions with other molecules or structural changes to cellular proteins.

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2,4-Dimethylbenzaldehyde oxime is a useful chemical for the synthesis of complex organic compounds. It is used as a research chemical and as a speciality chemical in the production of fine chemicals. 2,4-Dimethylbenzaldehyde oxime can be used as a versatile building block to form new compounds with different substituents. The compound has been shown to have high reactivity and good quality.

Butyraldoxime is a chemical that is used in the treatment of skin cancer. It has been shown to inhibit the growth of cultured human cells, including melanoma cells and leukemia cells. In vitro tests have shown that butyraldoxime inhibits sodium citrate-induced changes in cell morphology, an increase in cellular protein content and DNA synthesis, and an increase in tumor size. The mechanism of action for butyraldoxime is thought to be similar to that of the oxime inhibitor drugs. Oximes react with nitrite ion to form a reactive intermediate called nitrous acid, which reacts with caproic acid to form a nitric oxide radical. Nitric oxide radicals are then able to react with free methyl ethyl groups on the surface of cells and produce reactive oxygen species (ROS). ROS can cause damage to cell membranes, proteins and DNA within the cell. This damage may lead to cell death or inhibition of cellular function.

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50% in water; Average molecular weight 800 Da

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Applications N-Aminohexamethylenimine is a sesquiterpene lactones with anti-hepatitis C virus activity. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Rossini, M., et al.: Lett. Drug. Des. Discov., 9, 881 (2012); Hines, R.N., et al.: J. Pharmacol. Exp. Therap., 214, 88 (1980);

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4-Pyridinealdoxime is a compound that is synthesized by the reaction of chloride and pyridinium with copper complex in an organic solvent. It has been shown to inhibit the activity of glucose transporters (GLUTs) in vitro, and this effect is reversible. 4-Pyridinealdoxime interacts with GLUTs through hydrogen bonds, which may be responsible for its inhibitory effect. This drug has also been shown to reactivate supramolecular complexes. Structural formula: 4-Pyridinealdoxime {CoCl}·2HO → {CoCl}·2HO + {Co(OH)}·4HO → {Co(OH)}·4HO + 2HCl + 2NH3

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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