Heterocycles with Nitrogen (N)

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Applications N4-[5-[[4-[[5-(Acetylhydroxyamino)pentyl]amino]-1,4-dioxobutyl]hydroxyamino]pentyl]-N1-[5-[[3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)-1-oxopropyl]amino]pentyl]-N1-hydroxybutanediamide, is a bifunctional chelator.

2-Hydroxypyridine is a heterocyclic organic compound that contains a nitrogen atom and two hydrogen atoms. It is a proton donor and has been shown to be an effective inhibitor of HIV infection. 2-Hydroxypyridine also inhibits bacterial growth by inhibiting the synthesis of DNA and RNA, which prevents protein synthesis and cell division. The intramolecular hydrogen bonds in protonated 2-hydroxypyridine form tautomers that can change from one form to another, with the equilibrium depending on pH. 2-Hydroxypyridine is a natural compound found in picolinic acid or in plants such as parsley, black pepper, or cinnamon. X-ray crystal structures of 2-hydroxypyridine have revealed that it has a planar geometry with an intramolecular hydrogen bond between the nitrogen atom and the protonated carbon atom. This bond causes significant kinetic energy to be released during the reaction mechanism, which may

Please enquire for more information about (2R,4S)-Fmoc-4-hydroxypiperidine-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

6-Methyl-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidine-5-carbaldehyde is a white solid that has been found to be an intermediate in the synthesis of melamine. It has been analyzed by spectroscopy and found to contain substituents such as atropisomers and isomer. 6-Methyl-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidine-5-carbaldehyde can be formed by condensation between two anilines or through a steric reaction with porphyrin. This compound can also be synthesized in a dimer form with quinolines and substituted with n-.

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Please enquire for more information about 7-(1,3,5-Trimethyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidine-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

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4-Pyridoxic acid is a vitamin that is synthesized by the human body and found in food. It is an important cofactor for many enzyme reactions. 4-Pyridoxic acid also has antioxidant properties, which may be due to its ability to scavenge reactive oxygen species in the body. 4-Pyridoxic acid plays a role in energy metabolism, as it reacts with ATP to form ADP and pyridoxal phosphate. The recommended dosage of 4-pyridoxic acid is 50-200mg per day.

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N-(2-oxo-1,2-dihydropyrimidin-4-yl)isobutyramide (NODPA) is an initiator that can be used to synthesize acrylonitrile. It has been shown to initiate the polymerization of uracil and yields a crystalline product in the presence of triflate. NODPA is also an analog of 2-deoxyribose and has significant activity as an initiator for nucleoside synthesis. The anomeric mixture is also important in this process. In addition, NODPA can be used to synthesize carbohydrates through glycosylation reactions.

Please enquire for more information about Ethyl 2-(4-methylpiperazin-1-yl)propanoate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Please enquire for more information about N-(4-Chloro-7H-pyrrolo[2,3-d]pyrimidin-2-yl)-2,2-dimethylpropionamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 4-(4-Bromophenyl)piperidine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Please enquire for more information about {4-[4-(3-Methylbutanoyl)piperazin-1-yl]phenyl}amine including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Aminopyrimidine is an organic compound with the chemical formula CHN. It is a hydrogen bond donor and a weak base, which means it can form hydrogen bonds with other molecules but does not have a high affinity for them. 4-Aminopyrimidine also has a hydrochloric acid (HCl) molecule as its conjugate base. It is used in horticultural applications to control plant diseases caused by fungi or bacteria such as powdery mildew or rust. Hydroxyl groups are part of the chemical structure of 4-aminopyrimidine, which are important in iron homeostasis in plants. This compound may be toxic to plants at high concentrations, so it should not be used on crops that do not need treatment. The nitrogen atom in this molecule forms amide bonds with other compounds, which are crucial for antimicrobial activity. 4-Aminopyrimidine undergoes cycloaddition reactions and has been shown to inhibit the growth of

Please enquire for more information about (4-(1-Benzylpiperidin-4-Yloxy)-2-Chlorophenyl)Methanamine Dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-(Piperazin-1-yl)benzoic acid hydrochloride is a chemical intermediate that is used in the synthesis of pharmaceuticals. It has been shown to be a useful scaffold, and can be used as a reaction component and building block in the synthesis of complex compounds. 4-(Piperazin-1-yl)benzoic acid hydrochloride is also versatile, as it has been shown to be an intermediate for the synthesis of fine chemicals.

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2-Hydroxy-4-methylpyridine is a cyclotriphosphazene that has been shown to inhibit the growth of bacteria. It has been shown to have a gene sequence profile with a high degree of similarity to the genes for phenoxy group, chloride, phosphazene, and pyridine ring. The metabolic pathway for 2-Hydroxy-4-methylpyridine is not well understood. It may be metabolized by hydrolysis or oxidation before being excreted in urine. The binding site on the bacterial DNA for 2HMP is not yet known. It has not been determined if this drug interacts with any other ligands. 2-Hydroxy-4-methylpyridine does not bind to magnetic resonance imaging (MRI) equipment and does not appear to be toxic in rats when given orally at doses up to 2000 mg/kg/day.

Please enquire for more information about 1-(3,5-Di-O-benzoyl-2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-5-iodo-2,4(1H,3H)-pyrimidinedione including the price, delivery time and more detailed product information at the technical inquiry form on this page

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2-Methyl-5-nitropyridin-3-amine is a heterocyclic compound that is synthesized by the cyclization of 2-methylpyridine with sodium nitrite. The reaction product is hydrolyzed to yield the desired compound, 5-nitropyridine. The synthesis of this compound can be used as a target for organic synthesis.

Please enquire for more information about DX-600 trifluoroacetate 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-(4,6-Dimethylpyrimidin-2-yl)-N'-(4-methylphenyl)guanidine including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Pyrimidinecarboxaldehyde is an organic compound that is used in the synthesis of pyrazoles. It can be prepared by the reaction of ethylenediamine with molybdenum trioxide in ethanol, followed by hydrolysis of the amine. 4-Pyrimidinecarboxaldehyde can also be obtained from methylpyrazine by oxidation to methylpyrazone and subsequent reaction with magnesium oxide. The nature of 4-pyrimidinecarboxaldehyde’s molecular target is not yet known, but it has been shown to have antineoplastic properties.

Applications 5-(1H-Pyrrol-1-yl)-1H-benzo[d]imidazole-2-thiol (cas# 172152-53-3) is a useful research chemical.

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Applications (S)-Benzyl 2-(5-Bromo-1H-indole-3-carbonyl)pyrrolidine-1-carboxylate is an intermediate in the synthesis of ent-Eletriptan (E505005), an enantiomeric impurity of the serotonin 5-HTIB/ID receptor agonist Eletriptan (E505000). References Orita, A., et al.: Green Chem., 3, 13 (2001);

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This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Please enquire for more information about 2-Cyanopyrimidine-5-boronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Applications 5,6-Dichloro-1,3-benzoxazol-2-amine

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Please enquire for more information about 3-(5-Piperidin-3-yl-1,2,4-oxadiazol-3-yl)pyridine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Applications 3-(Aminomethyl)pyridine is a compound useful in organic synthesis. A pyridine derivative with vasodilating activity. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Uno, B. E., et al.: Adv. Syn. Catal., 360, 1719 (2018); Trcka, V., et al.: Pharmazie, 11, 242 (1956)

2-Phenylbenzimidazole is an organic compound with the chemical formula C6H5N. It has a nitro group, which makes it highly reactive to light. This property makes 2-Phenylbenzimidazole useful in photochemistry and as a precursor for other organic compounds. It is also used as an anthelmintic agent to control parasites such as roundworms, hookworms, and tapeworms. The process of obtaining 2-Phenylbenzimidazole requires hydrochloric acid and anhydrous sodium to be mixed together in a solution at a high temperature. The reaction mechanism of 2-Phenylbenzimidazole is not well understood, but evidence suggests that it may be due to hydrogen bonding between the inhibitor molecule and the reaction site on the enzyme. Kinetic data has shown that 2-Phenylbenzimidazole inhibits molecules by binding to them. Tit

Applications 4-(Dimethylamino)pyridin-1-ium ((2-Nitrophenyl)sulfonyl)(phenoxycarbonyl)amide is an intermediate used in the synthesis of Monosulfuron (M567185), which is a sulfonylurea herbicide that inhibits Acetohydroxyacid synthase enzyme. References Wang, J., et al.: J. Comput. Aided Mol. Des., 19, 801 (2005);