Heterociclos com Nitrogénio (N)

1-Methyl-2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid (1MDP) is a proton stabilizer that enhances the rate of reactions involving carboxylate anions. It is used in organic synthesis as a substrate for the generation of methylene carbanions and active methylene compounds. 1MDP has been shown to enhance the rate of reactions with metaperiodate in the presence of ultraviolet light and orotic acid, yielding uncharged products. 1MDP also has been shown to increase the stability of both aromatic and aliphatic carboxylates.

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Applications 2-(3-chlorophenyl)pyrimidine-4-carboxylic acid (cas# 1216604-60-2) is a useful research chemical.

4-Ethylpyrimidin-2-amine hydrochloride is a compound that exhibits unique characteristics such as light emission and chlorination. It is commonly used in the synthesis of various organic compounds, including furfural, enantiomers, alfuzosin, serotonin, and benzamides. This compound has also been studied for its viscosity properties and its potential applications in the field of aquilaria sinensis research. Additionally, 4-Ethylpyrimidin-2-amine hydrochloride is classified as a research chemical and has been found to have diverse uses in different industries. Its derivatives, such as pyrimidone and nitrile compounds, have shown promising results in various scientific studies. This compound is synthesized from streptomyces strains using hydride reactions. Please note that 4-Ethylpyrimidin-2-amine hydrochloride is intended for research purposes only and should not be used for human or animal consumption.

2,4-Dichloro-6-methylpyridine is a synthetic compound that has been shown to induce apoptosis in human cancer cells. It is believed that this drug works by inducing DNA damage and subsequent cell death. 2,4-Dichloro-6-methylpyridine binds to sulfur atoms in the pyridine nucleotide cycle and prevents the enzyme from functioning normally. It also inhibits the proliferation of tumor cells by binding to nucleophiles on DNA during replication. The anti-proliferative effects of 2,4-dichloro-6-methylpyridine are due to its ability to block a number of stages in the cell cycle.

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6-Bromopyridin-2-yl)methanol is a brominating reagent used in the synthesis of histidine and cyanuric acid. It has been shown to bind to metal ions via chelate ring, phenyl groups, and skeletal interactions. 6-Bromopyridin-2-yl)methanol forms ether linkages with carboxylic acid groups, making it an excellent solvent for ionic compounds. This compound also has optical properties that are dependent on the chloride counterion. 6-Bromopyridin-2-yl)methanol is bioinorganic and cryogenic, which makes it useful in hydrogen bonding probes.

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