Heterociclos com Nitrogénio (N)

5-Chloropyrimidin-ol is a formamide derivative that has been shown to be an intermediate in the synthesis of various drugs. It is a member of the class of enamines and can be used as a precursor for benzyl, ammonium salt, or chloroacetic acid ester. 5-Chloropyrimidin-ol can also be used as an intermediate to produce cycloalkyl compounds.

Please enquire for more information about (3-Amino-2-oxo-2h-pyridin-1-yl)-acetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 3-(piperidin-4-yl)-6-(pyrrolidin-1-yl)pyridazine (cas# 1955520-87-2) is a useful research chemical.

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N-Acetyl-3-hydroxyindole is a chemical compound that can be used as a building block for other organic compounds. It is an intermediate in the synthesis of 3-amino-2,4,6-trichloropyrimidine, which is used in the synthesis of some pharmaceuticals and pesticides. N-Acetyl-3-hydroxyindole has been shown to react with thiourea to yield 2-(3,4-dihydroxyphenyl)acetic acid. It also reacts with hydroxylamine to produce 2-(aminooxymethyl)pyrrolidinone. N-Acetyl-3-hydroxyindole has been shown to have antioxidant properties, which may be due to its ability to reduce lipid peroxidation and scavenge reactive oxygen species.

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5-Bromo-3-iodopyridin-2(1H)-one is a basic organic chemical that is used to synthesize other compounds. It can be produced by the palladium-catalyzed reaction of methanol and carbon monoxide in the presence of a base such as sodium ethoxide. The cyclization of 5-bromo-3-iodopyridin-2(1H)-one with phenylacetylene leads to the formation of 2,5-dibromopyridine. Carbonylative coupling with acetaldehyde also yields 2,5-dibromopyridine from 5-bromo-3-(4,4,5,5,-tetramethyl-[1,3,2]dioxaborolan)pyridinium chloride and acetaldehyde.

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4-Amino-6-methoxypyrimidine is an organic compound that has a hydrogen bond with the nitrogen atom in its structure. The nitrogen atom is bonded to two oxygen atoms, which are located on opposite sides of the carbon atom. This compound can be synthesized by reacting zinc powder with an organic ligand. The reaction mechanism is believed to involve the formation of a hydrogen bond between the bidentate ligand and the 4-amino-6-methoxypyrimidine. Crystal x-ray diffraction and ultraviolet absorption data suggest that this compound has a planar molecular geometry and contains anions as part of its structure.

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4-Fluoropyridin-2-ol is a heterocyclic compound that can be cleaved to form the ether. It has been shown to be an analog of uracil and has been used in the preparation of fluorinated compounds. 4-Fluoropyridin-2-ol can undergo oxidation to form a n-oxide, which possesses a heterocyclic ring with an oxygen atom at one of the positions. This compound has been used as a precursor for other preparations containing heterocyclic compounds, such as tetrafluoropyridine (TFMP).

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(2S,5S)-5-Hydroxy-2-piperidinecarboxylic acid is a synthetic compound with a chemical formula of C4H8N2O4. It is an acid derivative that can be synthesized by the reaction of (2S,5R)-5-hydroxy-2-piperidinecarboxylic acid with hydrochloric acid in methanol. This compound has not been expressed in any organism, but it has shown antiinflammatory effects in mice.

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2,6-Pyridinedicarbonitrile (2,6-PDC) is a chemical species that belongs to the class of x-ray absorption. It is an ester hydrochloride salt with triazine and pyridine compounds. 2,6-Pyridinedicarbonitrile has been shown to be a homogeneous catalyst for the electrochemical oxidation of hydrogen peroxide. This compound has also been used in solid-phase synthesis as a hydrogen bond donor to form supramolecular structures. 2,6-Pyridinedicarbonitrile is stable in air and water but reacts with oxidizing agents such as chlorine, bromine, iodine, nitric acid, or perchlorates.

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Applications An intemediate of Clopidogrel and Prasugrel. References Yadav, G., et al.: Biochem. Eng. J., 19, 101(2004), Wang, P., et al.: Enzyme Microb. Technol., 39, 930 (2006),

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H-Imidazoleacetic acid is a synthetic compound that can be used to produce other compounds. It is soluble in water and has a hydrophilic interaction with calcium carbonate. H-Imidazoleacetic acid may be recycled, as it is easily synthesized from ethyl bromoacetate by reaction with hydrochloric acid. This substance has shown anticancer activity and may be used to treat blood pressure. The chromatographic method for H-Imidazoleacetic acid involves the use of extracellular medium to remove the organic solvent, followed by reversed phase chromatography on an ion exchange column. H-Imidazoleacetic acid is soluble in water and has a hydrophilic interaction with calcium carbonate. It may be recycled, as it is easily synthesized from ethyl bromoacetate by reaction with hydrochloric acid. This substance has shown anticancer activity and may be used to treat blood pressure. The

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4-Mercaptopiperidine-1-carboxylic acid tert-butyl ester is a potent and selective inhibitor of influenza virus. It has been shown to be the most potent inhibitor of influenza virus in a series of structurally modified piperidines, with an IC50 value of 0.4 microM. This compound can inhibit the activity of influenza viruses by binding to the viral M2 ion channel and blocking the efflux of sodium ions from the cells. 4-Mercaptopiperidine-1-carboxylic acid tert-butyl ester was also found to be active against other RNA viruses, such as poliovirus, dengue virus, and West Nile virus infections. The compound has been shown to inhibit these viruses by binding to their M2 ion channel and blocking sodium efflux. 4-Mercaptopiperidine-1-carboxylic acid tert-butyl ester has also been shown to have antiviral activity against HIV infection

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(E)-3-(Dimethylamino)-1-(pyridin-4-yl)prop-2-en-1-one is a compound that has potential applications in various fields including pharmaceuticals, research chemicals, and solid acid catalysts. Its structural formula indicates its ability to attenuate enzymatic cleavage, making it useful in enzyme-cleavable systems. This compound has been studied for its inhibitory effects on lipid peroxidation, which is associated with oxidative stress and various diseases. Additionally, (E)-3-(Dimethylamino)-1-(pyridin-4-yl)prop-2-en-1-one has shown potential as an emission activator for hydrogen fluoride and chloride ions. Its versatility makes it a valuable compound for researchers and professionals in different industries.

Lercanidipine is a calcium antagonist that binds to the calcium channels in the membranes of cells, preventing the entry of calcium ions. Lercanidipine is water soluble and can be synthesized using techniques such as elemental analysis and pharmacological techniques. It is also an ionizable drug, which means that its affinity for chloride varies with pH. Lercanidipine has been shown to have strong affinity for erythrocyte membranes and thus has a high selectivity for vascular smooth muscle cells. This drug also has a low toxicity profile and does not affect tissues other than vascular smooth muscle cells.

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5-BroMo-4-chloro-2-(Methylthio)-7H-Pyrrolo[2,3-d]pyriMidine is a nucleoside that can be used as an intermediate in the synthesis of other nucleosides. It has been shown to be a potent inhibitor of bacterial growth, including Mycobacterium tuberculosis and Escherichia coli. The chloride substituents on this molecule are deprotected by treatment with HCl to yield the desired product.

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2-Cyano-3-trifluoromethylpyridine is a fine chemical that is used as a versatile building block in the synthesis of complex compounds. It can be used as an intermediate in research chemicals, reaction components, and speciality chemicals. 2-Cyano-3-trifluoromethylpyridine is a high quality reagent that can be used for the synthesis of various derivatives. It is also a useful scaffold for the development of new drugs and other chemical compounds.

Applications 5-Bromo-2-(1H-tetrazol-5-yl)pyridine is a reagent in the synthesis and antibacterial activity of oxazolidinones containing pyridine substituted with heteroaromatic ring. References Jo, Y.W., et al.: Bioorg. Med. Chem., 12, 5909 (2004)

3-Amino-2-methylpyridine is a validated acetylating agent, which is stereoselective and thermodynamically stable. It reacts with nitro compounds to form an active analog that can be used as a pesticide. 3-Amino-2-methylpyridine also has the ability to inhibit protozoan parasites by binding to their bromodomain protein. The reaction yield for this compound is high, and it does not react in the presence of water or alcohols. 3-Amino-2-methylpyridine has been shown to have hydrogen bonding properties and contains functional groups such as amide, amine, and ether.

4,5-Dihydro-4-oxofuro[3,2-c]pyridine is a photocycloaddition product of acrylonitrile and cyclopentadiene. It has been used to study the reactivity of carbonyl groups in nucleophilic substitution reactions. The nuclear magnetic resonance (NMR) spectrum of 4,5-dihydro-4-oxofuro[3,2-c]pyridine consists of two signals at δ=7.32 and 7.07 ppm. These signals correspond to the two possible diastereomers of this compound: The C=O group is observed at δ=157 ppm in this compound's 13C NMR spectrum. This signal corresponds to the signal for the carbon atom attached to the double bond in the molecule. The magnetic resonance spectroscopy (MRS) shows that 4,5-dihydro-4-

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Applications 2-Hydroxy-1,3-oxazole-5-carboxylic acid