Heterocycles with Nitrogen (N)

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4-Fluoropyridine is a pyridine derivative that is synthesized by the reaction of hydrogen fluoride with 4-methylpyridine. It has been shown to have optical properties, with an absorption maximum of 565 nm and emission maximum at 637 nm. It also has a variety of methods for synthesis, including fluorination, chlorination, sulfoxidation, or acylation. 4-Fluoropyridine can be stabilized as an n-oxide in the presence of oxygen gas and isomers are possible. This compound has been shown to be activated by heat and then react with a sulfoxide to form a new heterostructure. The mechanism of death in this compound involves the formation of reactive oxygen species that cause DNA damage which leads to apoptosis.

2,4-Dihydroxy-5,6-dimethylpyrimidine is an inhibitor that is used in the synthesis of organic compounds. It reacts with aldehydes to form stable and reactive acylium ions. These acylium ions can then react with electrophiles, such as ketones, esters, and amines to form new products. 2,4-Dihydroxy-5,6-dimethylpyrimidine is usually used at neutral pH and has a reaction rate of about 10 M/s for the formation of an acylium ion from an aldehyde. This compound also reacts with nitrogen atoms on the aromatic ring to form a bidentate ligand that coordinates to the metal atom in the reaction mechanism of nitration.

2-Hydroxy-4-methylpyrimidine HCI is a crystalline solid that belongs to the group of organic compounds. It has a molecular formula of C5H5N3O2 and a molecular weight of 137.15 g/mol. The crystal structure is stabilized by hydrogen bonding between the hydroxyl groups on the molecules and water molecules present in the crystal lattice. Crystals are found in orthorhombic form, meaning they have three axes at right angles to each other with lengths that are not equal.

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2-Chloro-5-methoxypyrimidine is an industrial chemical that is used to produce other chemicals. It can be prepared by the reaction of tribromide with 2,5-dimethoxybenzaldehyde in the presence of a base. The yield of this reaction is optimized by using a solvent extraction method. The pale yellow solid obtained in this process can be purified by recrystallization from methanol.

2-Ethoxy-3-ethylpyrazine is a synthetic compound that has been shown to have an odorant binding affinity for the receptor protein 2. It has a high concentration in coatings and is used as an odorant in perfumes and deodorants. 2-Ethoxy-3-ethylpyrazine has been shown to have a strong effect on mammalian behavior when it is present at high concentrations. The behavioral response to this chemical was studied by laser ablation of the olfactory epithelium and granule cells in the nose of experimental rats. This chemical is also found in human lung tissue where it may play a role in chemotaxis, or the movement of leukocytes (white blood cells) towards sites of injury or infection. 2-Ethoxy-3-ethylpyrazine can be synthesized from ethyl pyruvate and chloroethane. A polymerase chain reaction assay was used to identify this chemical in polyacrylam

5-Azaindole is a heterocyclic compound that has been studied for its biological properties. It is a prodrug of trifluoroacetic acid, which can be used to treat metabolic disorders and autoimmune diseases. 5-Azaindole has also been shown to increase the expression of growth factor in cells, which may be useful in treating pain or bowel disease. This drug is metabolized by hydroxylation followed by conjugation with glucuronic acid and excretion in the urine. 5-Azaindole is also converted to an active form by enzymatic oxidation of a hydroxyl group and protonation on the nitrogen atom, as well as conversion to sorafenib (a drug used to inhibit tumor growth).

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5-Chloro-2-iodopyridine is a nucleophilic compound that can be used in cross-coupling reactions to form carbon-carbon bonds. It has been shown to allosterically modulate the activity of metabotropic glutamate receptors (mGluRs), which are members of the G protein coupled receptor family. 5-Chloro-2-iodopyridine is also an isomeric compound that can be used for the synthesis of carboxylate derivatives.

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2-Chloro-4,6-diphenyl-pyrimidine is a postulated fluorescent molecule that has been synthesized and characterized. The molecule has a potential use in the detection of perchlorates and phenylsulfonyl amide. 2-Chloro-4,6-diphenyl-pyrimidine has transport properties that are comparable to those of pyrylium. It is also stable at high temperatures, making it suitable for use in mass spectrometry. 2-Chloro-4,6-diphenyl-pyrimidine has a safety profile that is comparable to other molecules with similar functional groups. It can be used in fluorescent assays with efficiencies between 0.1% and 10%.

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2-(4-Bromophenyl)pyridine is an ancillary chemical in the Suzuki coupling reaction. It is used as a photoactive reagent to detect and quantify biological samples, such as uv irradiation, linear response, and potential use. 2-(4-Bromophenyl)pyridine has been shown to be a good substrate for the detection of aryl chlorides. It can be used as an optical probe for the structural analysis of trifluoroacetic acid and luminescent materials.

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Tert-butyl 3-acetyl-4-oxopiperidine-1-carboxylate is a potent, selective, and orally active potassium channel blocker with high potency. It has been shown to have antidepressant and antiemetic effects in animal studies. Tert-butyl 3-acetyl-4-oxopiperidine-1-carboxylate binds to the Kv1.3 potassium channel, which is an important target for treating depression and nausea. It also blocks the 5HT6 serotonin receptor, which may contribute to its antidepressant activity. The drug is a linear tertiary amine that contains an intramolecular hydrogen bond between the acetylene oxygen and the nitrogen of the piperidine ring. This hydrogen bond stabilizes the molecule in a conformation that allows for potent binding to Kv1.3 channels.

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Applications 2-Chloropyridine (2-CPY) has been identified as a trace organic chemical in process streams, wastewater and even drinking water. Furthermore, it appears to be formed as a secondary pollutant during the decomposition of specific insecticides. 2-CPY was found to be genotoxic agent. 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 Demsia, G., et al.: Mutat. Res., 634, 32 (2007), Stapleton, D., et al.: Water Res., 43, 3964 (2009),

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Intermediate in the synthesis of alogliptin

Applications 2-(2-Thenylamino)pyridine is an intermediate in the synthesis of Methapyrilene Hydrochloride (M259970). Methapyrilene is used as antihistaminic agent. References Calandre, E.P., et al.: Clin. Pharmacol. Ther., 29, 527 (1981); Eastmond, D., et al.: Mutagenesis, 24, 341 (2009); Dertinger, S., et al.: Toxicol. Sci., 115, 401 (2010)

3-Aminopyridine-2-carbonitrile is a protein inhibitor that is used to treat metabolic disorders. It has been shown to inhibit the activation of mitogen-activated protein kinase, which plays a role in the inflammatory response. 3-Aminopyridine-2-carbonitrile inhibits atherosclerotic cardiovascular disease and HIV infection. 3-Aminopyridine-2-carbonitrile also has antimicrobial activity and has been shown to be effective against hiv infection in biological studies.

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1-(3-amino-pyridin-2-yl)ethanone is a versatile compound that falls under the category of Other Fine Chemicals. It is commonly used as an intermediate in the synthesis of various pyrazoles, cellulose derivatives, and tricyclic compounds. In the medical field, this compound shows potential in the treatment of neovascular glaucoma due to its ability to inhibit certain enzymes involved in the condition. Additionally, it has been studied as a research chemical for its active properties and potential therapeutic applications. The synthesis of 1-(3-amino-pyridin-2-yl)ethanone involves several steps, with one notable method being borohydride reduction. This reaction can be carried out under specific industrial conditions to yield high-quality enantiomer products. Overall, 1-(3-amino-pyridin-2-yl)ethanone is an important compound with wide-ranging applications in various industries and research fields

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2-Chlorothiazolo[4,5-b]pyridine is a pyridine ring with two chloro groups. It has been shown to be potent in vitro and has a high potency in vivo. 2-Chlorothiazolo[4,5-b]pyridine has been shown to bind to the histamine H3 receptor, which is responsible for regulating the release of histamine in the body. This drug also binds to the H3 receptor, which is responsible for regulating the release of histamine in the body. 2-Chlorothiazolo[4,5-b]pyridine may have antihistamine properties due to its ability to antagonize histamine receptors.

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Applications 6-(2,3-Difluorophenyl)picolinic acid

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Applications L, L'-Bisuccinimide is great oil antioxidant detergent compound. References Wen, Y., et al.: Faming Zhuanli Shenqing, (2020);

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