Heterociclos com Nitrogénio (N)

Methyl 2-[(1H-pyrrolo[2,3-b]pyridin-5-yl)oxy]-4-fluorobenzoate is a versatile building block that can be used as a reagent or speciality chemical. It has been shown to be useful in the synthesis of complex compounds and research chemicals. Methyl 2-[(1H-pyrrolo[2,3-b]pyridin-5-yl)oxy]-4-fluorobenzoate is an intermediate for the synthesis of various pharmaceuticals and agrochemicals. This compound may also act as a scaffold for drug design and development.

4-Piperidineacetic acid is a synthetic compound that can be found in the leaves of plants such as quinquefasciatus. It has been shown to have an anti-oxidant effect, which may be due to its ability to inhibit cancer cells and cholesterol synthesis. 4-Piperidineacetic acid has also been shown to have potent inhibition of mosquito larvae death, with a half maximal inhibitory concentration (IC50) of 3.2 μM. 4-Piperidineacetic acid also binds to functional groups on proteins and inhibits the metabolism of organic substances by hydrolysis or oxidation.

This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Suitable for battery materials development.

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3-Bromo-5-methylpyridine-4-carboxaldehyde is a pinacol ester that can be synthesized from the pyridine ring and acetaldehyde. It is a regioselective synthesis of 3-bromo-5-methylpyridine. The pinacol ester can be used as an intermediate in the synthesis of other compounds, such as antirrhinum alkaloids.

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2,3-Pyrazinedicarboxylic acid is a molecule that can be found in bacteria and is the product of an intramolecular hydrogen reaction. It has been shown to have antibacterial activity against a strain of Bacillus subtilis. 2,3-Pyrazinedicarboxylic acid has been shown to react with hydrochloric acid to form an acid complex. The intramolecular hydrogen bond of 2,3-pyrazinedicarboxylic acid makes it hydrophilic and therefore it is soluble in water. This molecule also has the ability to form hydrogen bonding interactions with other molecules. 2,3-Pyrazinedicarboxylic acid has been shown to have anti-inflammatory properties because it inhibits prostaglandin synthesis by inhibiting cyclooxygenase and lipoxygenase enzymes.

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5-Bromopyridine-2-carboxylic acid methyl ester is an enantiopure compound with a chemical diversity. It is used in the benzoate synthesis and has been shown to have hemolytic activity. 5-Bromopyridine-2-carboxylic acid methyl ester is also a metabolite of picolinic acid, which has been shown to be antimicrobial against various bacteria and fungi. The asymmetric synthesis of 5-bromopyridine-2-carboxylic acid methyl ester can be accomplished using a Suzuki coupling reaction. This process produces an enantiomer that exhibits nucleophilic properties. The hydrogen chloride salt of the enantiomer has mesomorphic properties and can be utilized as a component for polymers or as an antimicrobial agent.

Applications 7-(3-Bromophenyl)pyrazolo[1,5-a]pyrimidine-3-carbonitrile (cas# 933054-30-9) is a compound useful in organic synthesis.

Applications An intermediate in the preparation of Piperidinyloxy free radical derivatives. References Irie, O., et al.: Bioorg. Med. Chem. Lett., 18, 5280 (2008),

2-[(2-Chloro-4-nitrophenoxy)methyl]pyridine is a chemical compound used in the industrial process of alkaline hydrolysis. It is an intermediate product that can be synthesized from 2-chloro-4-nitrophenol and pyridine. The reaction is carried out under alkaline conditions, with high yield. The synthesis method has been published in 1947.

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5-Methylpyrimidin-4-amine is a prodrug that is converted to the active form, pyridoxal 5′-phosphate, by an enzyme in the body. It has been shown to have anticancer activity and can be used as a cancer therapy. This drug interacts with metal ions such as chloride and inhibits glycopeptide antibiotics. 5-Methylpyrimidin-4-amine may also act as a reductant or reactive amide.

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2,5-Dibromopyridine is a chemical compound that can be used as a coupling agent in palladium-catalyzed cross-coupling reactions. It is used on the surface of metal particles to increase the efficiency of the reaction, and has been shown to react with substrates such as sodium hydroxide solution, sodium carbonate, halides and hydroxides. 2,5-Dibromopyridine also reacts with benzoate to form a palladium complex. 2,5-Dibromopyridine can be used as an oxidant or reductant depending on the type of reaction it is being used in. It has redox potentials at -0.6 volts for oxidation and +0.6 volts for reduction.

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