Heterociclos con nitrógeno (N)

Applications 2-OXO-2,3-DIHYDRO-1H-BENZO[D]IMIDAZOL-5-YLBORONIC ACID (cas# 1194483-04-9) is a useful research chemical.

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2,4-Dichloro-5-fluoropyrimidine is an aromatic hydrocarbon that has been shown to inhibit the growth of mouse tumor cells in vitro. It also inhibits the production of amines by reacting with industrial chemicals and sodium carbonate. This compound has potent inhibitory activity against autoimmune diseases and cytotoxic potency on mcf-7 cells. Furthermore, 2,4-Dichloro-5-fluoropyrimidine has been shown to have a chlorinating effect on cancer cells.

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6-Chloro-2-(4-chloro-phenyl)-pyrimidine-4-carboxylic acid is a chemical substance with the molecular formula CHClN. It is a prodrug of 6-chloropurine, which inhibits the bacterial enzyme dihydrofolate reductase, leading to inhibition of DNA synthesis and cell death. This compound has been shown to be active against members of the genus Staphylococcus and Streptococcus, including methicillin resistant strains. 6-Chloro-2-(4-chloro-phenyl)-pyrimidine-4-carboxylic acid has also been shown to be active against invasive infections caused by S. pneumoniae and H. influenzae type b and may have potential for use in treating other infectious diseases that are polyunsaturated fatty acids sensitive.

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8-Hydroxyquinoline sulfate is a drug that has been used to study the cancer tissue response to various drugs. The 8-hydroxyl group in the molecule interacts with metals and forms chelate complexes, which may be the reason for its cytotoxic effect. 8-Hydroxyquinoline sulfate also inhibits mitochondrial membrane potential and blocks the receptor activity of some cell types. It has been shown to be significantly cytotoxic to HL-60 cells, as well as other cell lines.

Please enquire for more information about Methyl [1-(4-chlorobenzyl)piperidin-4-yl]acetate hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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2-Ethyl-2-imidazoline (2EI) is a chemical compound that is used as a solvent for xylene, zinc powder and other chemicals. It is also used in the production of amides, dodecylbenzenes, epoxy resins and polyurethanes. 2EI has been shown to cause the dehydrogenation of molybdenum. It has been found that 2EI can be synthesized by reacting molybdate with benzotriazole.

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4-Chloro-2,3-dimethylpyridine N-oxide is a chemical compound that belongs to the class of medicines. It is used in the manufacture of hydrogen peroxide, which is an oxidizing agent and a bleaching agent. 4-Chloro-2,3-dimethylpyridine N-oxide has been used as a reagent for organic synthesis and as a catalyst in organic reactions. This compound also has the ability to inhibit proton pumps, which are membrane proteins that pump protons across biological membranes. The presence of sodium impurities can lead to scaling problems because it affects the solubility of 4-chloro-2,3-dimethylpyridine N-oxide. The exothermic reaction with chlorine leads to the formation of chloride, sulfoxide, and chloride ions. These products are more soluble than 4-chloro-2,3-dimethylpyridine N-oxide itself.

Acefylline piperazine is a hydrogen-bonded molecule with the chemical formula C8H14N4O. It is an occlusive profile that inhibits human serum lipoprotein lipase and cardiac lipases. Acefylline piperazine has been shown to inhibit fatty acid and eosinophil cationic protein production in vitro. This drug also possesses anti-inflammatory properties, which may be due to its ability to inhibit the enzyme activity of lipoprotein lipase, thereby reducing the levels of fatty acids present in tissues. Acefylline piperazine has a molecular weight of 168.2 daltons, which is consistent with most drugs that are administered intravenously as pharmaceutical dosages.

6-Chloro-3-pyridinylacetic acid is a compound that belongs to the class of isothiocyanates. It has been shown to have anti-inflammatory, analgesic, and antipyretic properties in rats. The structural analysis of this compound reveals that it features a cavity with two chloride ions as ligands. This cavity is occupied by three molecules of trimethyltin hydroxide tetranuclear clusters. The supramolecular assembly of this complex leads to an unusual crystalline structure with an acid hydrazide group, which may be responsible for the observed biological activity.

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Please enquire for more information about 1-{2-Cyclobutyl-7-[(E)-2-(dimethylamino)vinyl][1,2,4]triazolo[1,5-a]pyrimidin-6-yl}ethanone including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 7-tert-Butyl 2-ethyl3-bromo-5,6-dihydroimidazo[1,2-a]pyrazine-2,7(8H)-dicarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2-(Chloromethyl)-5-fluoropyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2-Amino-4-phenylpyrimidine-5-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

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4-Acetylpiperidine-1-carboxylic acid tert-butyl ester is a tert-butyl ester of 4-acetylpiperidine. It can be prepared by the reaction of sodium azide with chloroform and tert-butyl alcohol. The resulting product is a white solid that can be used as an intermediate in organic synthesis.

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2,4,6-Tri(2,4-dihydroxyphenyl)-1,3,5-triazine is an organic solvent that is used in liquid chromatography as a mobile phase. It has been shown to be effective in the separation of different types of pollutants and can be used for the removal of acidic compounds from wastewater. The solvent can also be evaporated without leaving any residue and is not toxic to humans or aquatic life. 2,4,6-Tri(2,4-dihydroxyphenyl)-1,3,5-triazine has been shown to react with cyanuric chloride under Friedel-Crafts conditions. This reaction produces heteropolyacids and polychlorocyanurate salts that are useful for environmental purposes such as remediation of metals from contaminated soils.

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Pyrimidine-5-carboxaldehyde is a chiral compound that is often used as a building block in the synthesis of pyrimidine nucleosides, which are important in biological studies. It is also used to synthesize chiral compounds, such as chlorate. The compound's asymmetric synthesis, high reactivity and biological function make it an excellent candidate for use in asymmetric reactions. Pyrimidine-5-carboxaldehyde has been shown to be antiviral and antimicrobial, with a potency similar to that of muscarinic m1 receptor agonists.

2,3-Diphenylpyrazine is a heterocyclic compound that exists as a white crystalline solid. It has been shown to inhibit the growth of bacteria by binding to metal ions. This compound has been shown to be an effective inhibitor of bacterial growth in electrochemical studies and is also potentiodynamically active in organic media. 2,3-Diphenylpyrazine has been shown to have optical properties that are sensitive to its environment, which may be due to the presence of nitrogen atoms. The molecule also contains a chelate ring that can act as an electron acceptor or donor, giving it luminescent properties.

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Applications α-(2,3-Dimethylphenyl)-α-methyl-1H-imidazole-5-methanol is used as a reagent in the synthesis of Medetomidine (M203250); an α2-adrenergic agonist. Also a sedative and analgesic. References Scheinin, M., et al.: Br. J. Clin. Pharmacol., 24, 443 (1987); Stenberg, D., et al.: J. Vet. Pharmacol. Ther., 10, 319 (1987); Virtanen, R., et al.: Eur. J. Pharmacol., 150, 9 (1988); Cullen, L.K., et al.: Br. Vet. J., 152, 519 (1996); Chen, W., et al.: Faming Zhuanli Shenqing. CN 101921234 A 20101222. Dec 22, 2010

2,3,3-Trimethyl-4,5-benzo-3H-indole is a fine chemical that is used as a versatile building block for research chemicals and speciality chemicals. It can be used to synthesize drugs. 2,3,3-Trimethyl-4,5-benzo-3H-indole is also a reaction component in the synthesis of complex compounds with high quality.

Please enquire for more information about 1-(4-Chlorobenzyl)piperazin-2-one hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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3,6-Di(pyridin-2-yl)-1,2,4,5-tetrazine is a tetranuclear molecule that contains two heterocyclic rings. It is an aromatic compound with a low energy transfer and has been shown to have the ability to react with sodium salts in mda-mb-231 breast cancer cells. This reaction produces an unstable intermediate that can undergo chain reactions with other molecules of 3,6-di(pyridin-2-yl)-1,2,4,5-tetrazine. The activation energies for these reactions are found to be in the range of 4.8 to 5.8 kcal/mol. The polymerase chain reaction (PCR) technique has been used to study binding constants of 3,6-di(pyridin-2-yl)-1,2,4,5-tetrazine and DNA. Results show that this molecule binds more tightly

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4-Methoxypyridine is a pyridine molecule that has been shown to form an adduct with methanol in a Langmuir adsorption isotherm. This compound has low energy and forms a covalent bond with the solvent molecule. It also has two hydrogen bonds, one of which is intermolecular. 4-Methoxypyridine can be synthesized from methyl nicotinate and n-oxide by replacement of the hydrogen atom on nitrogen with oxygen. The reaction mechanism for this transformation involves the formation of a covalent bond between the methyl group and the oxygen atom followed by protonation of nitrogen to form an n-oxide. 4-Methoxypyridine can also be obtained from pyridinium by removing a proton from carbon, forming a neutral ph molecule with two intermolecular hydrogen bonds.br> br> 4-Methoxypyridine is used as an

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