Heterociclos con nitrógeno (N)

Please enquire for more information about 1-(2-Bromobutanoyl)-3,5-dimethylpiperidine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about N-(5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Piperidine-4-carboxylic acid(4-chloro-phenyl)-amide including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,2', 2'' -Terpyridine is a chelate ligand that is used in wastewater treatment. It can be synthesized by reacting 2-aminopyridine with ethylene diamine and 2,4-dichloro-1,3-dithiolane. The x-ray crystal structures of the ligand show that it has a coordination geometry of octahedral and its reaction mechanism is an oxidation. The chelate ligand binds to the metal ion in the same way as other ligands and stabilizes it by forming hydrogen bonds. This compound has significant cytotoxicity against carcinoma cell lines and also inhibits the mitochondrial membrane potential (MMP). 2,2', 2'' -Terpyridine is classified as group p2 due to its redox potentials and cytotoxicity.

Please enquire for more information about 2-(Cyclopropylamino)-6-methylpyrimidin-4(3H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 2-Acetylpyridine is an aroma and flavour compound present in foods. References Roberts, D. et al.: J. Agri. Food, Chem., 43, 2179 (1995); Buttery, R. et al.: J. Agri. Food Chem., 46, 2764 (1996);

Applications Ethyl (5-Ethyl-2-pyridinyl)-1,1-d2-acetate (cas# 1189654-25-8) is a compound useful in organic synthesis.

3-Methyl-2-pyridinecarboxaldehyde is a thione compound with pharmacokinetic properties that has been studied using mass spectrometry and asymmetric synthesis. This phenolic compound is a ligand that can form hydrogen bonds with metal ions. It was synthesized by reacting an imine with a carbonyl group, which generated the desired product in high yield. 3-Methyl-2-pyridinecarboxaldehyde has been found to be homologous to other compounds such as acetophenone and benzil.

3,5-Dichloro-4-pyridinecarbonitrile is a synthetic herbicide that is used to control weeds. It has been shown to be effective against velvetleaf and portulaca oleracea. This compound inhibits the biosynthesis of formic acid and prevents the formation of hydroxylamine, which is an important intermediate in the synthesis of chlorophyll. 3,5-Dichloro-4-pyridinecarbonitrile also exhibits a strong inhibitory activity against plant tissue culture cells.br> br> 3,5-Dichloro-4-pyridinecarbonitrile is an analog for hirsutum, thidiazuron and other herbicides. It binds to the enzyme acetohydroxyacid synthase (AHAS), inhibiting the production of shikimic acid from chorismate. The product of this reaction will be an intermediate in the synthesis of aromatic amino

Methyl 6-chloro-2-pyridinecarboxylate is a reactive, organic compound that belongs to the class of monomers. It is a white crystalline solid with a melting point of approximately 130 degrees Celsius. This chemical can be synthesized by reacting 2-chlorobenzothiazole with sodium carbonate in water at temperatures between 100 and 140 degrees Celsius. The reaction yields methyl 6-chloro-2-pyridinecarboxylate as well as chloride and picolinic acid as side products. This compound has been shown to have neurotoxic effects when administered to rats at high doses.

1-[2-Fluoro-3-Hydroxy-4-(Hydroxymethyl)Cyclopentyl]-5-Iodopyrimidine-2,4-Dione is a pyrimidine nucleoside analog that can be used as an antiviral agent. It is a membrane transport inhibitor with cardiac activity and has been shown to inhibit the growth of herpes simplex virus in tissue cultures. 1-[2-Fluoro-3-hydroxy-4-(hydroxymethyl)cyclopentyl]-5-iodopyrimidine-2,4-dione has also been shown to inhibit the uptake of thymidine by cells infected with type 1 viruses. This agent has also been shown to have cytotoxic effects on glioma cells and on bacterial strains such as Pseudomonas aeruginosa and Staphylococcus aureus.

5-Phenyl-1,2,3-triazine is an isomer of the 1,2,3-triazine class of heterocyclic compounds. It has been experimentally shown to exist in four conformations: two dihedral and two conformational. The dihedral isomers have a planar conformation with a plane of symmetry through the five-membered ring. The conformational isomers are nonplanar and possess a boat or chair conformation. These different conformations can lead to different optical properties. 5-Phenyl-1,2,3-triazine has a dipole moment due to its nitrogen atoms. This molecule also exhibits optical activity due to its asymmetric carbon atoms and the presence of hydroxyl groups on one side of the molecule. The relative orientation of these groups can also create anisotropy in the molecule's optical properties.

Please enquire for more information about Methyl 4-benzyl-N-cyanopiperidine-1-carbimidothioate including the price, delivery time and more detailed product information at the technical inquiry form on this page