Imines

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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.

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(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%.

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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

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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.]]

Applications A degradation product of herbicide Molinate in pot soil and rice plants. References Kriek, E., et al.: Biochemistry, 6, 177 (1967), Farmer, P., et al.: Toxicol. Lett., 149, 3 (2004), Gyorffy, E., et al.: Carcinogenesis, 25, 1201 (2004),

9-Anthraldoxime is an oxime that is used in the preparation of new synthetic strategies. It has been shown to be a precursor for a variety of functional groups and has been used in the synthesis of a variety of organic compounds. 9-Anthraldoxime is also an electron spin resonance (ESR) reagent and can be used in the study of electron spin resonance spectra. This chemical compound is also useful for examining functional groups, such as methyl groups, through its spectral data. Being an ESR reagent, it can be used to measure the nature of electrons and their spin orientation.

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(Z)-1-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl)ethanone oxime is an antifungal agent that inhibits the synthesis of ergosterol, a major constituent of fungal cell membranes. It has been shown to be active against a variety of fungi and yeasts. (Z)-1-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl)ethanone oxime also has antimicrobial activity against bacteria such as Staphylococcus aureus and Pseudomonas aeruginosa.

Applications 9,10-Dihydro-1-benzo[a]pyrene-7(8H)-one Oxime (cas# 88909-82-4) is a compound useful in organic synthesis.

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Pentane-2,3,4-trione 3-oxime is a chelating agent that binds to metal ions in aqueous solution. It has been shown to have an average second order rate constant of 1.5 × 10. The active substances are formed by the reaction between hydrogen chloride and chloride ion with a molecule containing a carbonyl group. Pentane-2,3,4-trione 3-oxime is used as a pharmaceutical preparation for the treatment of various bacterial infections and skin diseases. This compound also has an anti-inflammatory effect due to its ability to chelate metal ions and decrease the production of prostaglandins.

Please enquire for more information about 3-(4-Chlorophenyl)-1H-pyrazole-4-carbaldehyde oxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications Butyraldoxime (cas# 110-69-0) is a useful research chemical.

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DL-Methionine sulfoximine is a drug that blocks the synthesis of glutathione, an important antioxidant and detoxifying agent. DL-Methionine sulfoximine may be useful in preventing or treating eye disorders, such as age-related macular degeneration and retinitis pigmentosa. It also has been shown to have beneficial effects in animal models of epilepsy, Alzheimer’s disease, Parkinson's disease, and stroke. DL-Methionine sulfoximine has been shown to have beneficial effects in animal models of epilepsy, Alzheimer’s disease, Parkinson's disease, and stroke. This drug is being studied for its potential use in metabolic disorders such as diabetes and obesity.

Inhibitor of YB-1 nuclear translocation; anti-cancer

4-Bromo-alpha-chlorobenzaldoxime is an unsymmetrical derivative of the cycloaddition reaction with a 1,3-dipolar cycloaddition. It is made by reacting chloral with benzaldehyde in the presence of aluminum chloride. The product obtained is a crystalline solid that can be used as a starting material for the synthesis of other compounds. 4-Bromo-alpha-chlorobenzaldoxime has been used as a precursor for various organic syntheses, such as liquid crystals and isoxazole derivatives.

Applications (Z)-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)

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2-Adamantanoneoxime is a compound with two functional groups, the carbonyl group and the oxime group. It is a chemical reagent that can be used in laboratory experiments to form a coordination complex. 2-Adamantanoneoxime has been shown to have antiviral activity against influenza virus and Schistosoma haematobium, which are both helminth parasites. 2-Adamantanoneoxime is also an antifungal agent, with in vitro activity against Candida albicans.

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S,S-Diphenylsulfilimine monohydrate is a sulfilimine that is prepared by the reaction of diphenylchlorosulfide and an aldehyde. It is a synthetic reagent that is used in organic chemistry for transferring a sulfide to an alkene or alkyne group. The sulfilimines are nucleophilic and can be used as catalysts in reactions involving halides and alcohols. S,S-Diphenylsulfilimine Monohydrate has been shown to be effective in the transfer of thiol groups to terminal olefins, such as hexane, with good yields. This agent also catalyzes dehydration reactions with high yields.

4-Methoxybenzaldehyde oxime is a compound that has been shown to inhibit the activity of the COX-2 enzyme. It has been shown to be effective in animal models of inflammatory bowel disease and colitis. 4-Methoxybenzaldehyde oxime has also been shown to have an isolated yield from a phosphotungstic acid (PTA) extract, which is a byproduct of the production of other chemicals. 4-Methoxybenzaldehyde oxime is active against inflammatory diseases in animal models, but it has not yet been tested on humans.

Dimethylglyoxime is a pesticide that has been used to control insects and nematodes. It has been found to be effective in controlling mosquitoes, flies, and other pests. This compound is also used as an extractor in microextraction. Dimethylglyoxime is not toxic to humans and does not cause any adverse effects on the environment or human health. It can be used with chlorine for wastewater treatment.

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Methylthioacetaldoxime is a nitro compound that has an alkylthio group, which is a hydrochloric acid derivative. It is soluble in water and is not volatile. Methylthioacetaldoxime has been used as a backup for chlorinated pesticides to control pests such as mosquitoes and fruit flies. This chemical also has some carcinogenic properties, but they are less potent than other pesticides. Methylthioacetaldoxime can be synthesized by the reaction of dialkylamine with formaldehyde and sulfur trioxide gas. The polymerase chain reaction (PCR) process uses methylthioacetaldoxime to detect the presence of specific DNA sequences in a sample.

The covid-19 pandemic is a respiratory disease that has been widely reported in the United States and Europe. The virus is spread by coughing and sneezing, and it can be transmitted through the air. Covid-19 is a polyatomic molecule, which means that its atoms are not bonded together in a single molecule. The covid-19 pandemic is characterized by chest pain, fever, headache, nausea, vomiting, and diarrhea.

Applications 6,7-Dinitro-2,3-dihydro-benzo[1,4]dioxime (cas# 57356-48-6) is a compound useful in organic synthesis.

Veratraldoxime is a synthetic compound that is the diacetate ester of oxime and has been used in the treatment of inflammatory bowel disease. It has been shown to be effective in some patients, but not all, with ulcerative colitis. Veratraldoxime inhibits the production of inflammatory mediators by inhibiting the activity of cyclooxygenase-2 and lipoxygenase. This drug also has anti-inflammatory properties by inhibiting prostaglandin synthesis at the level of phospholipase A2 and cyclooxygenase-1. The mechanism of action for this drug is similar to that of other nonsteroidal anti-inflammatory drugs (NSAIDs). Veratraldoxime also inhibits protein synthesis by blocking the formation of amide bonds, thereby inhibiting bacterial growth. The oxidation products are responsible for its antibiotic properties. Veratraldoxime binds to copper chromite to form a coordination complex, which is

4-Nitrobenzaldehyde oxime is a phenylhydrazone derivative that is a potent cytotoxic agent. The 1,2-nitration of the benzene ring in 4-nitrobenzaldehyde oxime produces a reactive intermediate that reacts with nucleophilic groups on cellular macromolecules to produce DNA strand breaks and other types of damage. 4-Nitrobenzaldehyde oxime has been shown to have significant anticancer activity against leukemia cells in culture, as well as antibacterial and anticancer activity against Staphylococcus aureus and Escherichia coli.

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Pivalaldehydeoxime (PAOx) is a metal-selective chelator that binds to copper, zinc, and nickel ions. PAOx can also act as an inhibitor of nitrification by binding to the metal ion nitrite in the presence of ammonia. PAOx has been shown to inhibit cell apoptosis by promoting DNA repair and inhibiting production of reactive oxygen species. Pivalaldehydeoxime has been found in environmental samples containing pollutants such as carboxyamide, nitro compounds, amines, and bidentate ligands.

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(1E,3E)-1-(4-Fluorophenyl)-2-methyl-1-penten-3-one oxime is a novel painkiller that has been shown to be effective in acute and chronic models of pain. It acts by inhibiting the voltage gated sodium ion channels (NaV) on nociceptive sensory neurons. This inhibition leads to an attenuation of the response to noxious stimuli. The drug also has a translational effect on humans, which is important for future clinical trials. A double-blind crossover study with coinjection revealed that the drug was safe and well tolerated in healthy human volunteers. This drug could potentially be used for treatment of neuropathic pain, postoperative pain, and cancer pain.

The heterocycle alpha-chloro-2-nitrobenzaldoxime is a functional group that can be oriented in two different ways. The diversity of the product arises from the fact that it is possible to create new functional groups by substitution on the benzene ring and on the nitrogen. Heterocyclization of alpha-chloro-2-nitrobenzaldoxime can be achieved by using other heterocycles such as isoxazoles, which are readily available in large quantities, as building blocks. This reaction can be catalyzed by reductive means with sodium borohydride and methanol.

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Clarithromycin oxime is an erythromycin derivative that is a potent inhibitor of protein synthesis in bacteria. It contains a methylating group, which has been shown to be necessary for its antibacterial activity. Clarithromycin oxime inhibits the growth of filamentous fungi and can be used to treat infectious diseases caused by pyogenes and staphylococci. The effective dose is not known, but it should be administered orally or intravenously.

1-(3-Pyridyl)ethan-1-oneoxime is a synthetic compound that has been shown to inhibit butyrylcholinesterase. The molecular electrostatic potential of this compound is calculated using the MM2 program, and it is found to be -0.17 eV. It is predicted that 1-(3-Pyridyl)ethan-1-oneoxime will interact with anions such as ClO4-. The postulated interactions are based on connectivity and the kinetics of this molecule. Interaction energies are calculated using MM2, and they are found to be -0.22 eV for the acceptor and -0.04 eV for the cholinesterases.

3,5-Dimethylbenzaldehyde oxime is a white crystalline solid that is soluble in organic solvents. 3,5-Dimethylbenzaldehyde oxime reacts with water to produce hydrogen peroxide and formaldehyde. This reaction is an example of a dehydration reaction.

L-Buthionine-(S,R)-sulfoximine (BSO) is a glutathione-depleting agent that causes cell death by interrupting mitochondrial functions. BSO has been shown to be reactive with covalent linkages in polymer compositions and enzyme activities, which results in the inhibition of human osteosarcoma cells. It also has pro-apoptotic properties that have been demonstrated using multivariate logistic regression on taxol toxicity studies. Resistance to BSO is rare, but has been observed in breast cancer cells. The synergistic effect of BSO and other drugs, such as chemotherapeutic agents, is not well understood.

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2-Chloro-6-fluorobenzaldehyde oxime is the chemical compound with the formula ClCH=C(O)N(OH)Cl. It is a white solid that is soluble in water and ethanol. 2-Chloro-6-fluorobenzaldehyde oxime is used as a versatile building block in organic synthesis, for example as a reagent for the preparation of amides, esters, and nitriles. It is also useful as a reagent for the conversion of ketones to nitriles.

Acetoxime O-(2,4,6-Trimethylphenylsulfonate) is a reagent used in the preparation of hydroxylamine. It is prepared by reacting acetone with 2,4,6-trimethylaniline and anhydrous magnesium chloride. Acetoxime O-(2,4,6-trimethylphenylsulfonate) is insoluble in water and organic solvents such as hexane or chloroform. The rate of reaction depends on the type of substituent on the benzene ring. For example, when R=H, the rate of reaction is slowest; when R=Cl, the rate of reaction is fastest.

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2-Butanone oxime is a reactive chemical compound that is used as an intermediate in the production of glycol ethers and esters. The optimum concentration for this chemical is 0.1-0.2 M in methanol, ethanol, or acetone. It reacts with methyl ethyl ketoxime to form the corresponding oxime. 2-Butanone oxime has been shown to be toxic to rats at doses of 300 mg/kg body weight when administered intraperitoneally. This compound is not readily absorbed by inhalation or through the skin and can be detected in air samples using gas chromatography with a flame ionization detector. A simple analytical method for 2-butanone oxime was developed that uses chitosan quaternary ammonium as a stationary phase on a column packed with silica gel. The mobile phase consists of 1% acetic acid in water and the flow rate is 1 mL/min.

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Benzamidoxime hydrochloride is an activator that can be used in the synthesis of 6-membered alkylaryl compounds. It contains a six-membered amidine ring and a six-membered ring.

4-Fluorobenzaldehyde oxime is a phenylhydrazine derivative that reacts with an aromatic amine to form a ternary complex. The reaction time for this process is short, and the yield of the product is high. 4-Fluorobenzaldehyde oxime also reacts with an aromatic amine to form an ion-pair. It can react with acidic hydrogen donors such as peracids and it also has high hydrogen bonding interactions. 4-Fluorobenzaldehyde oxime is used in pharmacological agents as well as other chemical reactions, including halogenation.

2,4-Dimethoxybenzaldoxime is an aldoxime that has been used in the synthesis of formyl compounds. It is a synthetic molecule with a molecular weight of 192.2 g/mol and a melting point of 97°C. 2,4-Dimethoxybenzaldoxime is used to synthesize fulvenes, which are highly reactive molecules that have been shown to be useful in the study of formyl group reactivity. It also has been used as a photosensitizer for photochemical reactions. In addition, it can be used to prepare unsaturated alkyl compounds by reacting with alcohols in the presence of base or acid.