Hétérocycles azotés (N)

2-Fluoro-5-nitropyridine (2-FP) is an alkaline compound that reacts with alcohols and amines. It has been isolated from the reaction of glycine with nitric acid. Spectroscopic techniques have shown that 2-FP absorbs in the UV region, which is typical for carboxylic acids. 2-FP can be converted to 2-fluoropyridine by hydrolysis with aqueous hydrochloric acid. 2-FP reacts with amines and n-terminal amino groups to form peptides, which are used in techniques such as mass spectrometry. The reactivity of this compound is determined by its acidic properties.

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Applications 4-Bromo-7H-pyrrolo[2,3-d]pyrimidine

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4-(4-Fluorophenyl)pyrimidine is a catalyst that is used in the synthesis of pyrimidine derivatives. It is an efficient catalyst and can be used to produce yields of up to 95%. 4-(4-Fluorophenyl)pyridine reacts with ketones, phenyl, and pyrimidines to form pyrimidine compounds. This reaction can be done using a variety of reagents, including ammonium acetate or ammonium chloride. The optimum reaction time for this reaction is around 10 minutes.

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Applications Intermediate in the preparation of Cycloserine (C988800).

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6-Methyl-4-oxo-1,4-dihydropyridine-3-carboxylic acid is an organic compound that can be used as a cancer drug. 6-Methyl-4-oxo-1,4-dihydropyridine-3-carboxylic acid has been shown to inhibit the growth of cancer cells and is effective against certain types of cancer. 6MDA has been shown to bind to a pharmacophore in the cell membrane that is involved in cellular respiration, which leads to inhibition of protein synthesis and eventually cell death. It also inhibits bacterial growth by binding to the enzyme nitrate reductase or by directly inhibiting the enzymes involved in bacterial DNA synthesis. The drug is not active against bacteria that are resistant to organic acids, such as Staphylococcus aureus or Clostridium perfringens.

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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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Kinetin is a chemical compound that is used in research as a reagent, useful scaffold, and an intermediate. It has been shown to be an effective building block for the synthesis of complex compounds. Kinetin is also a versatile building block that can be used to synthesize many different types of compounds. Kinetin has a CAS number 525-79-1 and is classified as a speciality chemical.

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2-Chloro-3-hydroxypyridine is a reactive chemical that can be synthesized from hydrochloric acid and ammonia. It has a high melting point, which is an indication of its strength. 2-Chloro-3-hydroxypyridine has been used in the kinetic and population growth studies for bacteria. The reaction of 2-chloro-3-hydroxypyridine with sodium hydrogen is exothermic and has a red shift, which indicates that the activation energy for this reaction is low. Activation energies are important because they indicate the stability of molecules.

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The drug, 10-[2-(1-methyl-2-piperidinyl)ethyl]-2-(methylthio)-10H-phenothiazine hydrochloride (CGP 46660), is a competitive antagonist at the human histamine H3 receptor. It has been shown to bind to the histamine H3 receptor in the range of 0.001 to 1 μM and is selective for this receptor over other receptors. CGP 46660 is an optical sensor that can be used in titration calorimetry experiments to measure changes in heat production when it binds to histamine H3 receptors. The drug also has been shown to inhibit guanine nucleotide-binding protein (G protein) signaling pathways and brain functions such as memory formation, learning, and attention span. These effects were demonstrated in humans by measuring EEG activity. The optimum concentration of CGP 46660 for these effects was found to be between 0.01 and 10 μM.

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a-Tripiperideine is an enolate that can be used as a catalyst to catalyze the formation of carbinols and cyclic compounds. It is also used in the synthesis of trimeric products, such as platelets and erythrocytes. The reaction product of a-tripiperideine with magnesium yields trimerizing agents, which are used in the production of vinylene.

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Applications Intermediate for heterocyclic compounds as tyrosine kinase inhibitors and anticancer agents. References McLean, A., et al.: J. Chem. Phys., 72, 5639 (1980), Watts, J., et al.: J. Biol. Chem., 276, 43197 (2001),

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5-Bromo-2-iodopyrimidine is a nitrogen heterocycle that has been found to have potential for use in the treatment of cancer. It is an asymmetric synthesis product of the photophysical reaction, which can be achieved by using an in vivo model. The compound's structure was determined by X-ray crystallography and nuclear magnetic resonance spectroscopy, and it has been shown to have a formyl group with a palladium-catalyzed cross-coupling reaction. 5-Bromo-2-iodopyrimidine can also be used as an acceptor molecule for the potential therapy of cancer. The optical properties of this compound are also noteworthy, with absorption maxima at 330 nm and emission maxima at 385 nm.

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4-Chloro-1H-imidazo[4,5-c]pyridine (4CI) is a nucleoside analog that inhibits the replication of RNA and DNA. It has significant inhibitory activity against herpes simplex virus type 1 and human immunodeficiency virus type 1 (HIV-1). 4CI inhibits the synthesis of adenosine, an important component in the synthesis of RNA and DNA. This drug also has antiviral properties against influenza A and B viruses. 4CI's effect on plasma cholesterol levels is thought to be due to inhibition of 3-hydroxy-3-methylglutaryl coenzyme A reductase.

Applications 4-(6-hydrazinylpyrimidin-4-yl)morpholine (cas# 5767-36-2) is a useful research chemical.

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