Heterociclos con nitrógeno (N)

Please enquire for more information about 6-Chloro-N,N'-bis(4-ethoxyphenyl)-1,3,5-triazine-2,4-diamine including the price, delivery time and more detailed product information at the technical inquiry form on this page

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.

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

Please enquire for more information about 5-[2-(2-Thienyl)ethyl]-1,4,5,6-tetrahydro-1,3,5-triazine-2-thiol including the price, delivery time and more detailed product information at the technical inquiry form on this page

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.

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.