Heterocycles with Nitrogen (N)

Please enquire for more information about tert-butyl 4-oxo-2-(Trifluoromethyl)piperidine-1-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Chloro-3-cyano-6-(4-fluorophenyl)pyridine is a derivate of the pyridine ring. It is soluble in water and has been shown to be a potent inhibitor of the soluble guanylate cyclase, which is an enzyme that converts GTP to cGMP. This inhibition leads to reduced levels of cGMP in the blood stream and may be used for the treatment of cardiovascular disorders such as hypertension, myocardial infarction, or angina. 2-Chloro-3-cyano-6-(4-fluorophenyl)pyridine also binds with high affinity to ligands containing a furyl group, such as formyl and nucleophilic compounds. It can also be used as a fluorescent probe for protein labeling in electrophoresis gels.

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

Please enquire for more information about 3-CHLORO-2-FLUORO-4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)PYRIDINE including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 6-(Trifluoromethyl)pyrimidin-4-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 2-Cyano-3-hydroxypyridine

Please enquire for more information about 8-Fluoro-1,2,3,4-Tetrahydro-Pyrazino[1,2-a]Indole including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about (E)-1-Acetyl-N-(acetyloxy)-a-(5-fluoro-2-hydroxyphenyl)-4-piperidinemethanimine including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Ethoxy-5-fluoro-1H-pyrimidin-4-one is a chemical compound that can be synthesized in ethanol, ether, and ethyl formate. It is a white crystalline solid with a melting point of 164°C. The impurities are filtered out using filtration. This compound reacts with substance to produce crystallization. 2-Ethoxy-5-fluoro-1H-pyrimidin-4-one can also be synthesized by reacting trimethylamine and isourea.

Please enquire for more information about 4,4-Difluoroazepane Hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Tert-Butyl (1-(2-Methoxyethyl)-4-Oxo-4,5-Dihydro-1H-Pyrazolo[3,4-D]Pyrimidin-6-Yl)Methylcarbamate including the price, delivery time and more detailed product information at the technical inquiry form on this page

(4-Fluorophenyl)Methyl-Dimethyl-(Piperidin-1-Ylmethyl)Silane is a synergistic substance. It has been shown to have a synergistic effect with nonsteroidal anti-inflammatory drugs, such as flupirtine, in the treatment of nervous system diseases. The drug shows depressant activity on the central nervous system and cardiac effects. This substance also binds to a wide range of receptors, including muscarinic acetylcholine receptors (mAChRs). The binding of this substance to M2 mAChRs may account for its clinical effects. Furthermore, it has been shown to have a number of biological properties that are related to its chemical structure, making it a promising candidate for further research.

Please enquire for more information about N-(2-Phenylethyl)-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

Please enquire for more information about 2-Fluoro-1-Piperazin-1-Yl-Ethanone including the price, delivery time and more detailed product information at the technical inquiry form on this page

5,7-Dimethoxy-[1,2,4]triazolo[1,5-a]pyrimidin-2-amine is a compound that can be synthesized from potassium thiocyanate and ethyl chloroformate. The reaction proceeds via the condensation of the thiocyanate with ethyl chloroformate to form an intermediate chlorothiocyanate. This intermediate reacts with potassium chloride to form the final product. The condensation reaction is conducted dropwise to prevent the side reaction of formation of 5-chloro-2,4-diamino-6-(trichloromethyl)pyrimidine.

2-(1H-1,2,4-Triazol-3-yl)pyridine is an efficient method for the synthesis of tetranuclear metalloporphyrins. This compound has been found to exist in a metastable form and can be converted to a stable form by coordination chemistry with metal ions. 2-(1H-1,2,4-Triazol-3-yl)pyridine has been shown to be isomeric with other pyridines and can be used as a starting material for the synthesis of palladium complexes. The x-ray crystal structures of these compounds have also been determined. The nmr spectra of water molecules bound to sodium salts show that they are in the trans configuration.

Please enquire for more information about 6-Bromo-2-pyridin-4-ylquinoline-4-carbonyl chloride hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about tert-Butyl (3-formylpyridin-2-yl)carbamate 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-Chloro-5-iodo-7-(3-azido-3-deoxy-beta-D-ribofuranosyl)-7H-pyrrolo[2.3-d]pyrimidine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Hexahydropyridazine is a heterocyclic organic compound with the chemical formula (CH)N. It is a white crystalline solid that has been used as an antihypertensive medication and in the synthesis of other pharmaceuticals. Hexahydropyridazine's hydrogen atoms are located on nitrogen atoms, which makes it an aromatic heterocycle. The FT-IR spectrum of hexahydropyridazine shows peaks at 1754 cm-1 and 1452 cm-1, which correspond to the stretching vibrations of N-H and C=O groups respectively. This substance is soluble in water and reacts with metal hydroxides, hydrochloric acid, and glucocorticoid receptors. Hexahydropyridazine can also be synthesized from trifluoromethanesulfonic acid and inorganic acids such as sulfuric acid or phosphoric acid.

Please enquire for more information about 1-[3-(2-Methoxy-4-nitrophenoxy)propyl]piperidine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Propan-2-ol - [2-(1-benzyl-1,2,3,6-tetrahydropyridin-4-yl)ethyl]amine (1:1) dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

6,7-Dihydrothieno[3,2-c]pyridine is a synthetic compound which has been used as a starting material in the synthesis of clopidogrel. 6,7-Dihydrothieno[3,2-c]pyridine has been shown to be an inhibitor of platelet aggregation. It is also a bifunctional compound that can act as either an acid or base catalyst. This property has led to its use in organic chemistry as a means of converting nitro groups into amines. The synthesis pathway for 6,7-dihydrothieno[3,2-c]pyridine begins with 5-azaindole and ends with the desired product after two steps: hydrogen sulfate reduction and hydrolysis.

Please enquire for more information about 1-[2-(Diphenylmethoxy)ethyl]piperazine dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Ethyl 3-pyrimidin-5-yl[1,2,4]triazolo[4,3-a]pyridine-6-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Dipyrazino[2,3-f:2',3'-h]quinoxaline is a heterocyclic compound that is synthesized by reacting 2-chloro-5-(trifluoromethyl)benzaldehyde with 3-aminophenol. It has a redox potential of 0.12 V and can undergo oxidation reactions in alkaline solution. Dipyrazino[2,3-f:2',3'-h]quinoxaline has been shown to have an electron deficient group in the pyrrole ring, which reacts with electron rich groups found in other molecules such as water. This reaction is irreversible and results in the formation of oxidized dipyrazino[2,3-f:2',3'-h]quinoxaline. Dipyrazino[2,3-f:2',3'-h]quinoxaline has been synthesized using x-ray crystallography techniques and nmr spectroscopy to

2-Chloropyridine-5-boronic acid is a boronic acid that is used in the synthesis of heteroaryl compounds. It can be synthesized by the Wittig reaction, which involves the reaction of an aldehyde or ketone with an alkene and phosphorane to form a ylide. 2-Chloropyridine-5-boronic acid can also be prepared by cross-coupling reactions between two different functional groups. These reactions include the palladium-catalyzed cross coupling and Suzuki cross coupling. This compound has been shown to be efficient for making furyl compounds using X-ray crystal structures.

2-Amino-5-hydroxypyridine is an analytical method used to measure the production of inflammatory cytokines, such as tumor necrosis factor alpha (TNF-α), in response to dextran sulfate. The 2-amino group acts as a proton acceptor and the 5-hydroxypyridine moiety acts as a nucleophile. The reaction between these two groups forms a hydroxyl group that can be detected using infrared spectroscopy. This method is capable of detecting TNF-α levels in vivo during bowel disease treatment. It has been shown that inflamed tissues produce more TNF-α than healthy tissues, so this test may be useful for monitoring inflammatory bowel disease activity and measuring the effectiveness of treatments for this condition. 2-Amino-5-hydroxypyridine has also been shown to act as an effective analgesic when combined with hydrochloric acid and hydroxyl group, which are necessary

Please enquire for more information about 6-(Methoxymethyl)-2-(methylthio)pyrimidin-4-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Chloro-1-methyl-1H-pyrrolo[3,2-c]pyridine is an analogue of ellipticine. It binds to the DNA and inhibits transcription. This drug has shown potential as a cancer chemotherapeutic agent.

Please enquire for more information about 3-Phenyl[1,2,4]triazolo[4,3-b]pyridazine-6-thiol including the price, delivery time and more detailed product information at the technical inquiry form on this page

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 6-Ethyl-7-methyl-2-pyrrolidin-1-yl[1,2,4]triazolo[1,5-a]pyrimidin-5(4H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2-(2-Pyridin-2-yl-1H-indol-3-yl)ethanamine monohydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 5-Cyanopyrimidine (cas# 40805-79-6) is a compound useful in organic synthesis.

Please enquire for more information about tert-Butyl 4-(2-hydrazinopyrimidin-4-yl)piperazine-1-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 6-Bromoimidazo[1,2-a]pyrazine-3-carbaldehyde 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-Chloro-5,6,7,8-tetrahydro-2-(methylthio)pyrido[4,3-d]pyrimidine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 1-Boc-piperazine-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 1-(tert-Butyloxycarbonyl)-3-fluoro-4-aminopiperidine including the price, delivery time and more detailed product information at the technical inquiry form on this page

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

1-Boc-3-aminopiperidine is an aminopiperidine that is used as a feedstock in the manufacture of pharmaceuticals. It is an optical isomer of 1-Boc-4-aminopiperidine, which has been shown to be effective in the synthesis of arylated piperidines. The compound reacts with sodium hypochlorite and formamide to produce ethyl formate, carbamate, and citric acid. The reaction also produces chiral regiospecificity in the product. This drug has been immobilized on silica gel for use in organic synthesis.