Hétérocycles azotés (N)

Please enquire for more information about 1-Isopropyl-1H-pyrazolo[3,4-b]pyridin-5-amine 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-nitro-4-piperazin-1-ylbenzoate 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 2,4-Dichloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Bromo-2-fluoro-3-methylpyridine is a fine chemical that is used as a scaffold for building more complex compounds. This chemical can be used in the synthesis of sulfonamides, thiocarbamates, and other organic compounds. 5-Bromo-2-fluoro-3-methylpyridine is also a versatile intermediate that can be used in the production of research chemicals and speciality chemicals. The purity of this compound is high and it has been shown to be a useful reagent in various reactions.

Please enquire for more information about 1-(Chloroacetyl)-4-(4-methoxyphenyl)piperazine 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-Thienyl)imidazo[1,2-a]pyridin-3-amine 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-[(3,3-Dimethylbutanoyl)amino][1,2,4]triazolo[4,3-a]pyridine-8-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-(3-Methoxybenzyl)piperidin-4-yl]methylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page

The compound 1H-Pyrrolo[3,2-c]pyridin-4(5H)-one is an enantiomer that is used as a starting material for the synthesis of other drugs. The hydrochloride salt is used in the manufacture of pharmaceuticals. This drug has been shown to be a potent inhibitor of xanthine oxidase and may have potential use in the treatment of gout and hyperuricemia.

1-(2-Methylphenyl)piperazine 2HCl is a cholinergic agent that has been shown to increase the activity of acetylcholine in the brain. It has been used to study the effects of acetylcholine on locomotor activity and memory. 1-(2-Methylphenyl)piperazine 2HCl can be synthesized by reacting piperazine with paraformaldehyde. The synthesis of 1-(2-Methylphenyl)piperazine 2HCl is dependent on the alkyl substituents on the piperazine molecule, as well as whether or not it has an R group.

2-Ethoxypyridine is a vinyl ether that contains an ethoxycarbonyl group. It is used in the synthesis of other compounds because it reacts with nucleophiles and has a high nucleophilic character. 2-Ethoxypyridine typically reacts with halides, such as fluorine, to form the corresponding fluoride. This reaction is catalyzed by bases, such as pyridine. The elimination reaction of 2-ethoxypyridine is second order kinetics and can be described by the rate law: rate=kt[A][B] Where k is the first order rate constant, t is time in seconds and A and B are reactants in moles per liter.

2-Pyrrolidin-2-ylpyridine (2-PyPy) is a chiral ligand that binds to palladium complexes and is used as a catalyst in the enantioselective synthesis of allylic alcohols. 2-PyPy can be used as a chiral ligand for palladium catalysts, which are used in the asymmetric alkylation reactions of allylic substrates. This ligand can also be used for the enantioselective synthesis of malonate derivatives. 2-Pyrrolidin-2-ylpyridine has been found to be an effective catalyst for allylic alkylation reactions, with high selectivity and enantioselectivity.

1-[(tert-Butyl)oxycarbonyl]-3-(3,4-dichlorobenzyl)piperidine-3-carboxylic acid is a blocker that is used to treat high blood pressure. It blocks the action of angiotensin II, which causes vasoconstriction, and also blocks the release of renin from the kidneys. 1-[(tert-Butyl)oxycarbonyl]-3-(3,4-dichlorobenzyl)piperidine-3-carboxylic acid is a potent inhibitor of the enzyme branched chain aminotransferase (BCAT), which converts the amino acids leucine, valine, and isoleucine into their corresponding ketoacids. It does this by binding to an allosteric site on BCAT and prevents formation of an active complex with its substrates. This inhibition can lead to a decrease in blood pressure

Applications 2-PHENYLPIPERAZINE 2HCL (cas# 872139-22-5) is a useful research chemical.

2-PhenyLpiperazine is a cytotoxic compound that is used in the synthesis of other drugs. It can be synthesized by reacting 2-phenylpiperazine with hydrogen chloride and phenol in an organic solvent. 2-PhenyLpiperazine has been shown to cause muscle necrosis in animals. The cytotoxic effects of this drug are due to its ability to inhibit RNA synthesis, DNA synthesis, and protein synthesis. Chronic pain may also be due to the inhibition of prostaglandin synthesis.

Please enquire for more information about N,N-DiBoc-2-amino-4-bromopyridine 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-Bromo- 2, 5- bis(trifluoromethyl) pyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 5-(3-methylphenyl)imidazolidine-2,4-dione (cas# 187978-79-6) is a useful research chemical.

N-[2-(1-Piperidinyl)-5-(trifluoromethyl)phenyl]-4-pyridinecarboxamide is a new, potent inhibitor of the hepatitis C virus (HCV). It has synergistic effects with other antiviral agents and is effective against murine melanoma. N-[2-(1-Piperidinyl)-5-(trifluoromethyl)phenyl]-4-pyridinecarboxamide inhibits the HCV NS3/NS4A proteases and blocks HCV RNA replication by inhibiting the polymerase activity and blocking the synthesis of viral proteins. In vitro assays have shown that this drug has antiviral activity for a variety of viruses, including human immunodeficiency virus type 1 (HIV-1), herpes simplex virus type 2 (HSV-2), and influenza A virus. This drug also inhibits myeloid leukemia cells in vitro by dephosphorylating

1,3-Diacetylindole is an alkene that belongs to the class of organic compounds. It can be prepared by Friedel-Crafts acylation of cyclopentenone with formaldehyde and hydrogen chloride gas. The molecule has a molecular electrostatic potential of -0.8 eV and a molecular weight of 126.1 g/mol. 1,3-Diacetylindole has been shown to react with Grignard reagent in an electrochemical study. Additionally, it has been used as a starting material for the synthesis of other molecules such as 2-methylquinoline and 1,2-dihydroquinoline. The vibrational and spectral data for 1,3-diacetylindole have been obtained using both experimental and computational methods. These data are useful for understanding the structure and reactivity of this compound at the molecular level.br>br> br>br>

Please enquire for more information about 1-Methyl-2-oxo-1,2-dihydropyridine-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Amino-5-bromopyrimidine is a chemical compound that has the chemical formula C4H6N2O2. It is also known as 5-Bromo-2-(pyridin-2-yl)pyrimidine. The nitrogen atoms in this molecule are incorporated into the pyrimidine ring, which consists of two six membered rings fused together to form a heterocycle. This heterocycle is substituted with two bromine atoms and one amine group. Additionally, the nitrogen atom adjacent to the amine group is not part of the pyrimidine ring and instead belongs to an amino group. 2-Amino-5-bromopyrimidine has been shown to be resistant to colistin, an antibiotic that targets bacterial cell wall synthesis. This drug has been shown to inhibit lipid kinase activity in vitro, which may lead to its use as a therapeutic agent for diseases such as diabetes mellitus type

2-Bromo-6-hydrazinopyridine hydrochloride is a salicylidene derivative that has anti-cancer properties. It is synthesized from the reaction of formaldehyde with salicylaldehyde, followed by hydrolysis of the resulting formamide with hydrazine. The product is an inorganic salt and a ligand for copper ions. 2-Bromo-6-hydrazinopyridine hydrochloride has been shown to inhibit cancer cell growth in vitro and in vivo, as well as to induce apoptosis in cancer cells. This drug also inhibits the synthesis of DNA, RNA, and protein. The analytical diffraction data on this drug show it forms a hexahydrate crystal structure at room temperature.

Please enquire for more information about tert-Butyl 2-ethynylpiperidine-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 Methyl 4-[(piperazin-1-ylacetyl)amino]benzoate 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 Deschloroethyl bendamustine 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 5-Chloro-3-(1-methyl-4-piperidinyl)indole including the price, delivery time and more detailed product information at the technical inquiry form on this page

5,6-Difluoro-2,4(1H,3H)-pyrimidinedione is a pyrimidine compound that has been shown to be an effective chemotherapy agent. It can be used to treat cancer cells by inhibiting DNA and RNA synthesis. This drug binds to thymine nucleosides and inhibits the activity of enzymes involved in the metabolic pathways that synthesize DNA and RNA. The drug also inhibits the production of thymidine monophosphate (TMP) through its inhibition of TMP synthase. 5,6-Difluoro-2,4(1H,3H)-pyrimidinedione is not active against normal cells because they do not contain thymine nucleosides. This compound is also soluble in trifluoroacetic acid and can be purified using dilution or preparative solvents.

Please enquire for more information about 4-Chloropyrido[4,3-d]pyrimidine including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-[4-[4-(4-Fluorophenyl)Piperazin-1-Yl]Butyl]-1-(4-Methoxyphenyl)Indazol-3-One is a hydrophobic, targetable, reconstituted drug. It is not soluble in water. The drug is iontophoretically injected into the circumferential region of the prostate gland and then remains in place for up to 12 hours. This drug has been used as a diagnostic tool for prostate cancer. The nitrate salt of 2-[4-[4-(4-Fluorophenyl)Piperazin-1-Yl]Butyl]-1-(4-Methoxyphenyl)Indazol-3-One may be used as a diluent for devices that are implanted or injected. This drug binds to monolayers at high concentrations and can be used for diagnostic purposes.

2,4,6-Trichloro-5-nitropyrimidine is a purine derivative that inhibits the cell proliferation of cancer cells. It has been shown to inhibit the activity of kinases and to induce apoptosis in human cancer cells in vitro. This drug also has antiproliferative potential against erythrocytes and is being investigated as a treatment for renal disease. 2,4,6-Trichloro-5-nitropyrimidine shows inhibitory effects on the phosphorylation of roscovitine by ATP and may be used to treat patients with glomerulonephritis. 2,4,6-Trichloro-5-nitropyrimidine can be synthesized from 2,4,6-trichloropyrimidinethiol and nitric acid according to the following equation: CClNO + HNO → CClNOH + NO 2 Cl + 3 HNO

Please enquire for more information about 4-Benzyl-5-[1-(ethylsulfonyl)piperidin-3-yl]-4H-1,2,4-triazole-3-thiol 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-(5-Bromopyrimidin-2-yl)ethanone 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-Piperidin-1-yl-1-phenylethylamine 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-(2,2,2-Trifluoroethyl)piperazine 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 2,2,6,6-Tetramethyl-4-(4'-toluenesulfonate)piperidinooxyl including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Ethyl-5-fluoropyrimidine is a white solid with a melting point of 258°C. It is soluble in organic solvents such as acetonitrile and methanol. The compound has been shown to have reversed phase chromatographic properties and can be used as a potential impurity in the synthesis of other compounds. 4-Ethyl-5-fluoropyrimidine is not susceptible to photolytic decomposition but can be oxidized by air, which may result in the formation of impurities. 4-Ethyl-5-fluoropyrimidine can be purified using chromatography methods with high sensitivity and low detection limits. The compound has also been shown to have good chemical stability under ambient conditions, making it suitable for storage or shipping.

Please enquire for more information about ethyl 2-(naphthalen-2-yl)-2-(piperidin-2-yl)acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Cyano-3-fluoropyridine is a reactive chemical that is found in the environment as a byproduct of industrial activity. It has been shown to be an allosteric modulator of hepg2 cells, which are responsible for producing glutamate. 2-Cyano-3-fluoropyridine has also been shown to inhibit the growth of tuberculosis and prostate cancer cells. The biological properties of 2-Cyano-3-fluoropyridine are similar to those of amide drugs, such as Valium, which are used for treating anxiety and other psychiatric disorders. 2-Cyano-3-fluoropyridine can react with benzyl groups to form homologous compounds that have been shown to have antihistamine effects.

Please enquire for more information about 2-Amino-[1,2,4]triazolo[1,5-a]pyridin-6-ol hydrobromide including the price, delivery time and more detailed product information at the technical inquiry form on this page

3,5-Difluoropyridine-2-carboxylic acid is the carboxylate form of 3,5-difluoropyridine. It has been used in the synthesis of antidiabetic drugs and devices. This compound is a ligand for a number of metal ions. 3,5-Difluoropyridine-2-carboxylic acid undergoes uptake by rat adipocytes and has been shown to be crystallographically active.

Applications 1-butylpiperidine-2-carboxylic acid (cas# 856838-98-7) is a useful research chemical.

Applications 4,6-Bis(4-nitrophenoxy)pyrimidine is an intermediate in the synthesis of N-[4-[(4-Ethyl-1-piperazinyl)methyl]-3-(trifluoromethyl)phenyl]-N'-[4-[[6-(methylamino)-4-pyrimidinyl]oxy]phenyl]urea (E926495), which is an inhibitor of RET, FLT3, KDR, c-Abl and c-Kit. Also, it prevent the growth of human thyroid cancer cells. References Weisberg, E., et al.: Genes Cancer, 1, 1021-1032 (2010);

Please enquire for more information about ([4-(Trifluoromethyl)Phenyl]Phenylmethyl)PiperazineDihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 8-Methyl-2-pyridin-4-ylquinoline-4-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 7-Bromo-1-methyl-1H-imidazo[4,5-c]pyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page

4,6-Dichloro-2-(pyridin-2-yl)pyrimidine is a pyridinium salt that is soluble in water. It has an elemental analysis of C, H, and N. Absorption spectroscopy showed that 4,6-Dichloro-2-(pyridin-2-yl)pyrimidine has an ionic nature with a quencher constant of 1.5×10. The absorption maximum was observed at 270 nm and the emission maximum was observed at 350 nm. There is no luminescence or fluorescence to this compound. Elemental analysis by ethylenediaminetetraacetic acid (EDTA) revealed the following: 0% Cl (chloride), 0% H (hydrogen), and 100% O (oxygen). EDTA also revealed that there are no impurities present in the sample which have been detected by UV/Vis spectroscopy. This

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

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