Heterocycles with Nitrogen (N)

Please enquire for more information about N-(2-Bromophenyl)-N'-(4,6-dimethylpyrimidin-2-yl)guanidine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Methyl 4-(4-pyridinyl)benzoate is a ligand that selectively binds to the axial site of the metal ion. The coordination of this ligand is supramolecular and tetracarboxylate. It has an axial ligand with a square geometry and a carboxylate group at its axial position. Methyl 4-(4-pyridinyl)benzoate coordinates to the metal ion in an axial fashion, which allows for selective binding to various metal ions.

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Ethyl 2-aminopyridine-3-carboxylate is a white to yellow crystalline solid that is soluble in polar organic solvents such as formamide and dimethyl sulfoxide. It can be recrystallized from ethyl bromoacetate, formamide, and anhydrous sodium carbonate. The compound is a quinoline derivative synthesized by the Wittig reaction of ethyl bromoacetate and methyl acetoacetate with n-hexane as the solvent. This product has been used to study platelet function in blood plasma because it inhibits the aggregation of platelets in vitro. Ethyl 2-aminopyridine-3-carboxylate also inhibits the synthesis of proteins in bacteria and is used as an antimicrobial agent.

Pyrimidine, 4-methoxy-6-methyl-, is an ionic liquid that has been shown to inhibit the growth of aldehyde and acid ester. It has also been found to inhibit tobacco mosaic virus and influenza A virus. This compound also displays biological activity in the form of an ester compound. Pyrimidine, 4-methoxy-6-methyl-, has a heterocyclic ring with an ionic group bonded to a heterocycle. The heterocyclic ring is substituted with two methyl groups, one on the nitrogen atom and one on the oxygen atom adjacent to the nitrogen atom. The chemical formula for this compound is CH3OCH2N(CH3)2OCH3.

Applications 2,2,6,6-Tetramethyl-1-hydroxypiperidine is a reactant used in various synthesis and investigations. It was used as a reactant in the study of predicting organic hydrogen atom transfer rate constants using the Marcus cross relation. 2,2,6,6-Tetramethyl-1-hydroxypiperidine was also used as a reactant in the preparation of ammonia from an iron nitrido complex. References Scepaniak, J., et al.: Angew. Chem. Int. Ed., 48, 3158 (2009); Warren, J., Mayer, J.: Proc. Natl. Acad. Sci. U.S.A., 107, 5282 (2010);

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The 2,4-difluoropyrimidine molecule is an iterative molecule with a fluorine atom at the 2,4 position. It has potential for several applications, including photochemical reactions and ionization. This molecule has been studied in detail by correlating its photoelectron spectra with theoretical calculations. The 2,4-difluoropyrimidine can be used as a starting material for other molecules of interest.

1,4-Dihydro-2,6-dimethyl-4-[2-(trifluoromethyl)phenyl]-3,5-pyridinedicarboxylic acid 3-ethyl 5-[2-[[4-[3-(trifluoromethyl)-3H-diazir in-3-yl]benzoyl]amino]ethyl] ester is an anticancer drug that inhibits the glycoside hydrolase enzyme. This drug also binds to a transporter protein and blocks its function. 1,4-Dihydro-2,6-dimethyl-4-[2-(trifluoromethyl)phenyl]-3,5-pyridinedicarboxylic acid 3-ethyl 5-[2-[(4-[3-(trifluoromethyl)-3H--diazir in--3--yl]benzoyl)