Imines

Please enquire for more information about (1Z)-1-(3,4,5-Trimethoxyphenyl)ethanone oxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

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.

Please enquire for more information about Sodium 2'-hydroxyacetophenone oxime-2-sulphinate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about (5E)-1,2,3,4,10,11-Hexahydro-5H-spiro[benzo[c]pyrano[3,2-g]chromene-9,1'-cyclohexan]-5-one oxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

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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.

Please enquire for more information about N-Formylhexamethyleneimine dimethylacetal including the price, delivery time and more detailed product information at the technical inquiry form on this page

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.

Please enquire for more information about 9-anthraldehyde oxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

(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.

Please enquire for more information about Cefuroxime sodium impurity F including the price, delivery time and more detailed product information at the technical inquiry form on this page

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

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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.

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

Please enquire for more information about Cefuroxime EP Impurity G including the price, delivery time and more detailed product information at the technical inquiry form on this page

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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Please enquire for more information about 1-Ethylimidazolidine-2,4,5-trione5-(o-methyloxime) including the price, delivery time and more detailed product information at the technical inquiry form on this page

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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.

Please enquire for more information about (3E)-5-Ethyl-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

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.

Please enquire for more information about (1E)-1-(9H-Fluoren-2-yl)ethanone oxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Trans-benzaldoxime is an analytical reagent that is used to determine the protease activity of pharmaceutical preparations. It reacts with the amino acid residues of proteins and converts them into a fluorescent product, which can be measured using a spectrophotometer. Trans-benzaldoxime is used in the kinetic determination of oxidative DNA damage. It has been shown to react with the hydroxyl group of glycol ethers in coordination complexes and form a glycol ether adduct, which can be detected by mass spectrometry. Reaction mechanisms for trans-benzaldoxime include oxidation and hydrolysis.

9-Fluorenone oxime is a pharmacological agent that has been shown to inhibit the activity of proteases. It has been shown to be effective in the treatment of hepatitis caused by radiation and amines, such as fluorenone. 9-Fluorenone oxime binds to the hydroxyl group of the active site on the protease enzyme and forms a covalent bond with it. This prevents hydrolysis of substrate proteins and thus blocks protein synthesis. 9-Fluorenone oxime also has chelate ligand properties, which allow it to bind to metal ions, such as phosphotungstic acid or fluorescence probes, and form complexes. The thermal expansion property of 9-fluorenones can be used for thermometry in biochemistry research.