Heterocycles with Nitrogen (N)

<p>5-Pyridin-2-yl-2H-pyrazol-3-ylamine is a chemical intermediate that can be used in the synthesis of many different compounds. This compound is a versatile building block that can be used to make complex substances, as well as being an excellent reagent for research purposes. It has been shown to be useful as a reactant in the preparation of high quality chemicals and speciality chemicals. 5-Pyridin-2-yl-2H-pyrazol-3-ylamine is a fine chemical with CAS No. 92352-29-9.</p>

<p>2,6-Dimethyl-1,4-diphenylpyridinium tetrafluoroborate is a high quality reagent that can be used as a useful intermediate in the synthesis of fine chemicals. It is used as an important building block in the synthesis of many organic compounds and is also an important reaction component. This compound has a wide range of uses and can be used as a versatile building block in organic synthesis or as a speciality chemical for research purposes.</p>

<p>5-Methoxyindole-3-acetic acid (5MI) is an endogenous indole and metabolite of melatonin that is found in high concentrations in the human serum. 5MI has been shown to inhibit the activity of cyclase enzymes and may be a specific inhibitor of the type I form of estrone sulfate, which is involved in estrogen production. This agent also inhibits matrix metalloproteinases and aminotransferases, which are enzymes that play a role in oxidative injury. 5MI also has a fluorescent derivative that can be used as a probe for biological samples or to study the target enzyme.</p>

<p>1-(3-Chlorophenyl)piperazine HCl is a drug that belongs to the group of pharmacological agents. It is used as an antidepressant and antipsychotic, and has been shown to decrease serotonin levels in the brain. 1-(3-Chlorophenyl)piperazine HCl is a potent 5-HT2C receptor agonist that inhibits ovarian activity in vitro. The compound has also been shown to be effective against trazodone and 5-HT2 receptors in vitro.</p>

<p>4,4'-Bis(methoxycarbonyl)-2,2'-bipyridine is a ligand that can be used in cross-coupling reactions. It has been shown to bind to metal ions and form complexes with the ligands. 4,4'-Bis(methoxycarbonyl)-2,2'-bipyridine has a constant value for maximizing the yield of the reaction and is luminescent. This product also has photophysical properties that allow it to be utilized in voltammetry studies. The transfer of this product can be optimized by using chromophores or catalysis. 4,4'-Bis(methoxycarbonyl)-2,2'-bipyridine provides a means for cross-coupling reactions using electrochemical studies and dichroism.</p>

<p>5-Bromo-6-chloro-1H-indole is a fine chemical that is used as a building block for research chemicals, reagents, and speciality chemicals. It is soluble in chloroform and benzene, but insoluble in water. This product can be used as a reaction component or a useful intermediate in the production of complex compounds. 5-Bromo-6-chloro-1H-indole has been reported to be an effective scaffold for the synthesis of many novel compounds with potential applications such as pharmaceuticals, agrochemicals, and dyes.</p>

<p>N-tritylimidazole is a palladium complex that was designed as an inhibitor of glycosidases. It binds to the active site of these enzymes and inhibits their function. N-tritylimidazole has been shown to inhibit the growth of Gram-positive bacteria, such as Staphylococcus aureus, by preventing the production of extracellular polysaccharides. This compound also binds to κ-opioid receptors in the brain and has been shown to block pain transmission. N-tritylimidazole can be synthesized using a cross-coupling reaction with phenylboronic acid and chloroiodomethane, which requires hydrochloric acid as a catalyst.</p>

<p>2-Amino-4-fluoropyridine is an acylation reaction product of 2-amino-4-chloropyridine and a fatty acid. The diaminopyridine moiety is responsible for the inhibition of copper enzymes. In addition, fluorine substitution provides a higher operational stability. The synthesis of this compound is accomplished through the use of thionyl chloride in an operational procedure that includes heating at 180 °C for 4 hours. 2-Amino-4-fluoropyridine has been shown to be effective against some bacteria such as Mycobacterium tuberculosis and Legionella pneumophila, which are resistant to other agents. This drug also has antiplasmodial properties and can be used to treat malaria. The structure based design of this molecule was optimized by replacing chlorine with fluorine as well as introducing a n oxide group to provide a sterically more favorable conformation.</p>

<p>2,4-Pyridinedicarboxylic acid diethyl ester is an aliphatic hydrocarbon that has been shown to be a potent active oxygen scavenger. It has also been shown to inhibit the uptake of fatty acids and organic anions by tubule cells in the liver, as well as to reduce collagen breakdown in the endoplasmic reticulum. This compound is converted into pyridinedicarboxylic acid, which inhibits hepcidin production and thus increases iron absorption. 2,4-Pyridinedicarboxylic acid diethyl ester also has a biochemical profile that is similar to that of a lipophilic fatty acid ester.</p>

<p>4-Chloro-3-pyridinesulfonamide is an antibacterial sulfonamide that inhibits the enzyme carbonic anhydrase. It has been shown to inhibit the growth of cancer cells in vitro and in vivo. The anticancer effect may be due to its ability to block the growth of cancer cells by interfering with DNA synthesis and inducing apoptosis, which causes cell death. 4-Chloro-3-pyridinesulfonamide also inhibits tuberculosis and tuberculostatic activity may be due to its inhibition of mycobacterium tuberculosis ribosomes. 4-Chloro-3-pyridinesulfonamide binds to the active site of bacterial anhydrase as well as human carbonic anhydrase II, blocking the conversion of CO2 into bicarbonate ions, which leads to a decrease in pH. This drug also binds to DNA and RNA, inhibiting DNA synthesis and RNA synthesis respectively, leading to cell</p>

<p>2,2'-Bipyridine-6-carboxylic acid is a reagent that is used in organic synthesis as a reaction component and building block for the synthesis of heterocyclic compounds. 2,2'-Bipyridine-6-carboxylic acid is also used as a precursor to produce other compounds. 2,2'-Bipyridine-6-carboxylic acid has been shown to be useful in the synthesis of complex compounds with diverse structures, making it a versatile building block. It can also be used as an intermediate in the synthesis of various drugs and speciality chemicals.</p>

<p>2-Iodopyridine is an organic compound with the chemical formula C5H5N. It is a white crystalline solid that is soluble in water, alcohol, and ether. The molecule contains a methyl group and two iodine atoms. 2-Iodopyridine has several industrial uses. It acts as a precursor to various pharmaceuticals and agrochemicals. The compound also exhibits insulin resistance properties, which may be related to its ability to bind to the insulin receptor and inhibit insulin signaling. 2-Iodopyridine can also be used for treating cancer because it binds to the DNA of cancer cells, preventing replication and leading to cell death.</p>

<p>5-Pyridin-2-yl-1H-pyridin-2-one is a chemical compound that belongs to the group of reactive dyes. It is a stable process that can be used for coupling with methoxy groups. This product has been shown to be a stable, high yield chemical that can be used in industrial large scale production. It is also considered an environmentally safe chemical because it does not pollute the environment and has low toxicity. 5-Pyridin-2-yl-1H-pyridin-2-one undergoes bromination reactions and has been shown to have nucleophilic properties.</p>

<p>1-(2-Methoxyphenyl)piperazine hydrochloride is a drug that belongs to the class of sulfonamides. It is used in the treatment of bacterial infections, especially those caused by methicillin-resistant Staphylococcus aureus (MRSA). The use of 1-(2-Methoxyphenyl)piperazine hydrochloride has been shown to be effective in reducing the symptoms of depression and anxiety and may be useful in the treatment of Parkinson's disease. The drug binds to 5-HT7 receptors, which are expressed on serotonergic neurons, leading to increased levels of serotonin and dopamine. This effect on serotonin receptors may lead to an increase in appetite and weight gain. 1-(2-Methoxyphenyl)piperazine hydrochloride also blocks the multidrug efflux pump, which is responsible for pumping out drugs from cells. This leads to an increase in intracellular concentrations of</p>

<p>4-Hydrazinopiperidine dihydrochloride is a versatile chemical compound that can be used as a reagent and as a building block in organic synthesis. It is also an intermediate for the production of pharmaceuticals, dyes, and pesticides. 4-Hydrazinopiperidine dihydrochloride is a fine chemical that has been approved by the U.S. Food and Drug Administration (FDA) for use in food contact applications, such as polymers, coatings, adhesives and sealants.</p>

<p>3,5,6-Trichloro-4-hydroxy-2-picolinic acid is a high quality reagent that is used as a building block for the synthesis of complex compounds with potential pharmaceutical applications. It can be used as an intermediate in the production of fine chemicals and speciality chemicals. This compound is also useful for research purposes and as a versatile building block for reactions.</p>

<p>2,3-Diethyl-5-methylpyrazine is a methyl ketone that is used as a model for fatty acids. It has been shown to be an important precursor for the synthesis of unsaturated ketones. 2,3-Diethyl-5-methylpyrazine can be produced by the reaction of acetone with ethylene and then subjected to acid catalyzed cyclization. This compound also has a characteristic odor that has been described as "fruity" or "spicy." It is used in the production of butyric acid, which is an important industrial chemical.</p>

<p>4-Methoxy-2,3,5-trimethylpyridine is an efficient hydrogenolysis catalyst that can be used for the synthesis of ethers from alcohols. It is a member of the methoxides family and can be produced by condensation of chloroform with acetaldehyde and formaldehyde. 4-Methoxy-2,3,5-trimethylpyridine inhibits palladium chloride from catalyzing hydrogenation reactions. The compound also has an inhibiting activity against acidic amines and n-Oxides. Its high yield makes it useful in organic synthesis as a precursor to diethyl malonate.</p>

<p>Please enquire for more information about trans-4-Propyl-L-proline including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(6-Methylpyridin-2-yl)ethyl]amine is a reagent that is used as a building block for the synthesis of heterocycles. It is used in the preparation of various complex compounds, such as 2-(6-methylpyridin-2-yl)ethylamine hydrochloride, 2-(6-methylpyridin-2-yl)ethylamine hydrobromide, and 2-[(6-methylpyridin-2-yl)ethyl]amine hydrochloride. This chemical can be used as an intermediate in the synthesis of fine chemicals or speciality chemicals. It has CAS No. 19363-94-1 and is an important research chemical with versatile uses in organic synthesis reactions.</p>

<p>2-Cyano-1,5-dimethylpyrrole is a quinone antibiotic. It has been shown to have antibacterial activity against organisms such as Staphylococcus, Streptococcus, and Pyogenes. This chemical has been shown to be active in the gaseous phase and against test organisms in alcohol extracts. 2-Cyano-1,5-dimethylpyrrole also exhibits flavonoid and saponin properties that may contribute to its antimicrobial activity.</p>

<p>3-(Diethylboryl) pyridine is a halogenated biphenyl. It is used in the synthesis of 3-aryl substituted pyridines by cross-coupling reactions with aryl iodides, bromides and chlorides. Cross-coupling reactions are usually carried out at low temperatures (0 to 20°C) in order to minimize side reactions. The reaction is usually conducted in a biphasic system containing an organic solvent and water, which facilitates the extraction of the product from the mixture. 3-(Diethylboryl) pyridine reacts with halide ions via an electrophilic substitution reaction to form a reactive intermediate, which reacts with palladium catalyst to produce the desired product. This process is also called catalytic hydrogenation. 3-(Diethylboryl) pyridine has been shown to inhibit human cytochrome P450 enzymes, which are involved in drug metabolism and break down drugs</p>

<p>2-Chloro-5-hydroxymethylpyridine is a metabolite of the active substance 2-chloro-5,6-dihydroxymethylpyridine (mk-0674), which has been shown to inhibit cytochrome P450 enzymes. It is found in urine samples from patients treated with mk-0674 and can be used to monitor the efficacy of treatment. The biochemical properties of 2-chloro-5,6-dihydroxymethylpyridine have been studied in yeast cells and it has been shown that this compound is glucuronidated and excreted as a conjugate with glycine. The yeast strain Saccharomyces cerevisiae was used for these studies.</p>

<p>4-Methoxy-3-nitropyridine (4MNOP) is an organic compound that is a white solid at room temperature. 4MNOP has been shown to interact with alkali metals and can be used in the preparation of emulsifying agents. It also has been found to have pharmacokinetic properties, including a low molecular weight, good solubility in water, and a high degree of absorption. The imidazopyridine ring system is susceptible to reductive amination reactions, which may lead to the formation of amine or surfactant residues.</p>

<p>4-(4-Methylpiperazino)acetophenone is a chemical compound that can be used as a building block in the synthesis of more complex compounds. It is a versatile intermediate and can be used to synthesize other compounds. 4-(4-Methylpiperazino)acetophenone has been shown to act as a reaction component in the synthesis of pharmaceuticals, pesticides, and agrochemicals. This compound has high purity and quality.</p>

<p>4-Amino-pyridine-2-carboxylic acid methyl ester is a compound that is used as a reactant, reagent, and building block in organic synthesis. It is also useful for the preparation of complex compounds. 4-Amino-pyridine-2-carboxylic acid methyl ester is soluble in water and has a melting point of 183°C. The CAS number for this chemical is 71469-93-7.</p>

<p>Please enquire for more information about N-(3-Fluoro-4-piperidinyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>The aim of this study is to assess the effect of 4-Piperidinobutyric acid (4-PABA) on the efficiency of rats in a dietary model. The experimental design included two treatments with different levels of 4-PABA, and a control group with no supplementation. The experiment was conducted by feeding rats a diet with low protein content (6% casein), and measuring their weight gain, feed intake, and food conversion ratio (FCR). The results indicated that 4-PABA had no statistically significant effects on weight gain or feed intake. However, FCR was significantly higher for the high 4-PABA treatment group. These findings support the hypothesis that dietary protein is an important determinant in rat energy metabolism.</p>

<p>4-Benzoylpyridine is a reactive molecule that can undergo electron reduction and protonation. The protonated form of 4-benzoylpyridine has been shown to inhibit the enzyme methionine aminopeptidase, which is involved in the degradation of amino acids. The crystallographic structure of 4-benzoylpyridine was determined by X-ray diffraction and was found to contain nitrogen atoms at the center of its ring. The electron density map showed that there are no hydrogen bonds or lone pairs in 4-benzoylpyridine. This molecule is an inhibitor of the transfer reactions in mitochondria, which are required for ATP synthesis. It has been shown to be cytotoxic to mammalian cells in culture and may have photochemical properties.</p>

<p>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</p>

<p>6-Ethylmercaptopurine is a purine analogue that inhibits the synthesis of DNA. It is used as an inhibitor of protein synthesis and in the treatment of inflammatory bowel disease. 6-Ethylmercaptopurine has been shown to inhibit the activity of ATPase, which may be responsible for its ability to suppress the proliferation of cells. This drug can also act as an analog to adenosine, which can be used to determine ATP levels in a cell or tissue sample by measuring the amount of p-nitrophenyl phosphate produced. 6-Ethylmercaptopurine has been shown to block phosphatase activity, which may lead to inflammation in some cases.<br>6-Ethylmercaptopurine has a molecular weight of 194.2 g/mol and an optimum pH of 4.5</p>

<p>1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide is a bifunctional organometallic compound. It is used as a catalyst in the reduction of nitro groups or other electron-deficient centers and in the transfer process with azides. This chemical has shown selectivity for aliphatic substrates over aromatic ones. The catalytic activity of 1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide can be enhanced by replacing the hydrogen atom on the nitrogen atom with an alkene group. 1,1'-Di-n-octyl-4,4'-bipyridinium Dibromide is also a radical cation that can be reduced by electron donors to form radicals.</p>

<p>Please enquire for more information about 5,6-Diaminobenzimidazole dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Piperazin-1-yl-benzo[d]isothiazole hydrochloride is an atypical antipsychotic that belongs to the group of inorganic compounds. It has been shown to have a high affinity for acidic surfaces and can be used in industrial applications such as the removal of metal ions from water by filtration. 3-Piperazin-1-yl-benzo[d]isothiazole hydrochloride is synthesized by reacting an inorganic base with a piperazine compound, followed by hydrolysis of the piperazine ring using acid. Impurities are often found during synthesis, which may contain traces of other compounds such as pyridine or methylamine.</p>

<p>6-Bromo-2,3-dihydro-1H-indole is a natural product that has been shown to inhibit cancer cell growth in vitro. In the presence of 6-bromoindole, cells are unable to proliferate and undergo apoptosis. This compound also shows anti-cancer activity against human leukemia cells. The mechanism of action for this molecule is not yet known but may be related to its ability to activate the caspase enzyme family or its ability to bind to DNA. 6-Bromoindole has been shown to have anti-inflammatory properties through inhibition of prostaglandin synthesis in animal models.</p>

<p>4-Methoxy-3,5-dimethyl-pyridin-2-yl)methyl acetate is a chemical intermediate that is used in the manufacture of pharmaceuticals and other fine chemicals. It has been found to be a useful scaffold for the synthesis of other compounds. This compound may also be used as a building block or reaction component in research. 4-Methoxy-3,5-dimethyl-pyridin-2-yl)methyl acetate has a CAS number of 91219-90-8 and can be purchased from suppliers such as TCI America.</p>

<p>2-Cyanopyrazine is a molecule that belongs to the group of nitrogen-containing heterocyclic compounds. It has been shown to exhibit antiinflammatory activity in skin cancer cells and bacterial strain, group P2. This compound inhibits the growth of bacteria by binding to their pyrazinoic acid, which is an electron acceptor. 2-Cyanopyrazine also exhibits tuberculostatic activity against M. tuberculosis and M. avium complex by inhibiting the synthesis of mycolic acids and cell wall lipids, respectively. The redox cycle of this compound is coordinated with a hydrogen bond between the hydroxyl group and the carbonyl carbon atom. 2-Cyanopyrazine is oxidized from its initial state through a reaction mechanism involving molecular oxygen or hydrogen peroxide as an oxidant and water as a reductant. The oxidation products can be reduced back to 2-cyanoapyrazine using ascorbate or NADH as</p>

<p>2'-(4-Ethoxyphenyl)-5-(4-methyl-1-piperazinyl)-2,5'-bi-1H-benzimidazole trihydrochloride (EPMB) is a DNA binding agent that is used in tumor detection and research into apoptosis. It has been shown to inhibit the activity of p-glycoprotein, which is an efflux pump protein, and Bcl-2 protein. EPMB has also been shown to cause apoptosis in human squamous cell carcinoma cells in a concentration dependent manner. This compound has shown potential as a treatment for cancer because it inhibits the ability of cancer cells to proliferate by binding to the NMDA receptor.</p>

<p>4-Amino-3-chloro-2,5,6-trifluoropyridine is a reactive and unstable chemical compound that belongs to the group of anilines. It is used in the synthesis of hypsochromic dyes. The compound has been shown to interact with other molecules, such as chemo-, supramolecular-, and synthetically-. The fluorophore has been stabilized by a supramolecular approach. Chemically induced fluorescence properties have been observed for 4-amino-3-chloro-2,5,6-trifluoropyridine.</p>

<p>2,6-Dichloro-3-nitropyridine is a nitro compound that is used to synthesize the drug flupirtine. Flupirtine has been shown to be effective in treating hepatitis C and prostate cancer cells. It inhibits glycogen synthase kinase-3 (GSK-3) by binding to the ATP site on the enzyme, which prevents phosphorylation of its substrate proteins and leads to cell death. 2,6-Dichloro-3-nitropyridine can also inhibit pim-1 and ammonolysis, two enzymes involved in DNA damage repair.</p>

<p>2-Amino-4,6-dihydroxy-5-methylpyrimidine is a versatile building block that can be used in the synthesis of complex compounds. It has CAS No. 55477-35-5 and can be used as a reagent or speciality chemical for research purposes. 2-Amino-4,6-dihydroxy-5-methylpyrimidine is also useful for the synthesis of reaction components and scaffolds for high quality compounds.</p>

<p>2,2'-Bipyridine-3,3'-dicarboxylic acid is a coordination compound that contains two carboxylic acid groups. It forms a dihydrate in water and is orthorhombic in crystal form. The molecule can be represented by the following chemical structure:</p>

<p>6-Bromo-7-azaindole is a homologous molecule. It is an electron deficient compound with a piperidine moiety at the 6 position and a nitrogen atom at the 7 position. The nitrogen atom substitutes for an oxygen atom, making this molecule reactive. The electron deficient nature of this molecule makes it suitable for use in transistors and other physicochemical devices. 6-Bromo-7-azaindole has been shown to be effective against carcinoma cells in vitro, as well as to inhibit tumor growth in vivo. This drug also causes homologous recombination by interacting with DNA in mammalian cells. 6-Bromo-7-azaindole binds to DNA, forming a covalent bond with the guanine base of DNA through the nitrogen atom, which is electron deficient.</p>

<p>Building block for preparation of heteroaryltriazole derivatives</p>

<p>2-(2,4-Difluorophenyl)pyridine (2DPP) is a x-ray crystal structure that has been shown to be ancillary and have anticancer activity. 2DPP has a redox potential of -0.52 V, which is high resistance against reduction. It is also an aldehyde group with two nitrogen atoms and two hydrochloric acid groups. 2DPP can produce light emission in the presence of chloride and picolinic acid and has been shown to be photophysics. The structural analysis of 2DPP reveals that it has a molecular weight of 184.07 g/mol and a melting point of 272 degrees Celsius. This compound also binds to mitochondrial membranes in the presence of light, which is responsible for its optical properties.</p>

<p>2-Chlorobenzimidazole is an analog of benzimidazole that has been synthesized by Langmuir adsorption isotherm. It is a white crystalline solid that can be dissolved in water and hydrochloric acid. 2-Chlorobenzimidazole inhibits the growth of herpes simplex virus by acting as a competitive inhibitor for the viral enzyme thymidine kinase, which catalyzes the conversion of thymine to thymidine. 2-Chlorobenzimidazole also binds to monoclonal antibodies, inhibiting their binding to their corresponding antigens. This activity may be due to its ability to bind covalently with amino groups on proteins and other molecules. Magnetic resonance spectroscopy has shown that 2-chlorobenzimidazole binds tightly with protonated (positively charged) phosphorous atoms within cells.</p>

<p>1-(5-Chloro-2-methoxyphenyl)piperazine HCl is a fine chemical that belongs to the group of research chemicals. It is used as a reagent, speciality chemical and intermediate in organic synthesis. 1-(5-Chloro-2-methoxyphenyl)piperazine HCl is an effective building block for complex compounds, which can be used in reactions involving acetals, amides, nitriles, sulfones, sulfonamides and imines. This compound also has versatile building blocks and is a useful scaffold in organic synthesis.</p>

<p>3-Amino-4-bromopyridine is a receptor binding ligand that belongs to the group of synthetic, active natural products. It has been shown to stabilize nicotinic acetylcholine receptors and inhibit the release of acetylcholine. 3-Amino-4-bromopyridine has been shown to be a potent antagonist at nicotinic acetylcholine receptors and can be used in the treatment of disorders such as Parkinson's disease, Alzheimer's disease, and schizophrenia. 3-Amino-4-bromopyridine binds to pyridiniums in an inorganic acid environment and stabilizes them, which prevents their interaction with carbolines that are important for the modulation of neuronal activity.</p>

<p>Tetrahydro-1,3-dimethyl-1H-pyrimidin-2-one is an organic compound that is used in the synthesis of drugs and other organic compounds. It can be synthesized by reacting hydrogen fluoride with nitrogen atoms. Tetrahydro-1,3-dimethyl-1H-pyrimidin-2-one can form stable complexes with iodination reactions and has been used to prepare monoclonal antibodies. This molecule has also been studied using x-ray crystal structures and titration calorimetry to investigate its reaction mechanism. The light emission from this molecule is due to intermolecular hydrogen bonding between a pyrazole ring and a phenyl ring.</p>

<p>Please enquire for more information about 1-Ethyl-1,2-dihydro-2,2,4-trimethyl-7-quinolinol hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,5,6-Triamino-4-hydroxypyrimidine (THP) is a nitrogenous base that has been shown to have anticancer activity. It is an intermediate in the biosynthesis of lysine and can be found in environmental pollution. THP is formed by the reaction of hydrogen chloride with dimethylformamide, which produces hydrochloric acid as a byproduct. 2,5,6-Triamino-4-hydroxypyrimidine also reacts with glyoxal to produce a compound that can cause metabolic disorders. THP is an acidic compound that becomes neutral when dissolved in water. The molecular formula for THP is C 3 H 6 N 8 O 4 .</p>

<p>3-Amino-5-bromo-2-chloropyridine is a synthetic compound that has been shown to be an inhibitor of phosphoinositide 3 kinase delta (PI3Kδ). It is also a potent inhibitor of the proliferation of human cancer cells in vitro and in vivo. The PI3Kδ is activated by insulin and other growth factors, which leads to the activation of downstream pathways. These pathways trigger cell growth and proliferation. 3-Amino-5-bromo-2-chloropyridine may have potential as a novel anticancer drug due to its ability to inhibit PI3Kδ activity and prevent the progression of cancer.</p>

<p>2-Methylimidazole is a crystalline solid that has been used in the preparation of coordination compounds. The compound is prepared by reacting 2-methylimidazole with an appropriate metal cyanide, such as copper cyanide or nickel cyanide. The crystal structure of 2-methylimidazole shows strong hydrogen bonding interaction between the nitrogen atoms and the carboxylate groups. This compound has been used in clinical pathology to detect increased levels of ammonia, uric acid, and lactic acid in the blood. 2-Methylimidazole is not toxic to humans but has shown some toxicity to mice when injected intravenously at high concentrations. It can be used as an analytical method for determining trace amounts of chlorine in chemical compounds by way of electrochemical impedance spectroscopy (EIS).</p>

<p>2-Chloro-4,5-diaminopyrimidine is a pyrimidine compound with the molecular formula CHClN. It can be synthesized by reacting glycine and phenol with piperidine in the presence of hydrochloric acid. 2-Chloro-4,5-diaminopyrimidine has a solubility of 1.2 g/100 mL in water and reacts with quinine to form a red solution. This product also reacts with proline to produce an orange solution that fluoresces green when exposed to UV light. 2-Chloro-4,5-diaminopyrimidine has been used as an intermediate in the synthesis of other compounds such as pyridoxal phosphate and cefixime.</p>

<p>1-Methyl-1H-imidazole-4-carboxylic acid methyl ester is a carboxylic acid that is aniline derivative with the chemical formula C6H5NCH2COOH. It is soluble in water, ethanol and acetone. 1-Methyl-1H-imidazole-4-carboxylic acid methyl ester hydrolyzes to form aniline and methanol. The reflux of 1-methyl imidazole can produce the same products as well as formaldehyde and hydrogen cyanide.</p>

<p>6-Chloropyridine-3-sulfonyl chloride is a synthetic compound that has been shown to be an inhibitor of the enzyme anhydrase, which is involved in the production of carbonic acid. This inhibition leads to a decrease in the pH of tissues and may inhibit the proliferation of malignant cancer cells. 6-Chloropyridine-3-sulfonyl chloride has also been shown to have anticancer activity against eukaryotes.</p>

<p>6-Nitroquinoline is a nucleophilic compound that reacts with nitroalkanes to form alkyl nitrites. It undergoes a bioreductive reaction, in which it is reduced to the corresponding amine by hydrogen peroxide and ammonia. 6-Nitroquinoline contains functional groups that can act as either electron donors or electron acceptors and is therefore reactive towards other compounds. The reaction mechanism involves nucleophilic attack at the carbon atom in the ring of the 6-nitroquinoline molecule, resulting in an addition product. 6-Nitroquinoline has been shown to react with fluorophores such as fluorescein, forming a fluorescent product that can be detected by spectroscopy. This chemical can also form hydrogen bonds with other molecules, which are important for its reactivity. The reaction products of this compound are nitrite and quinolines where one or more of the nitrogens have been oxidized to nitro groups.<br>END</p>

<p>1-(2-(4-(Chloromethyl)phenoxy)ethyl)azepane HCl is a versatile building block that can be used as a reagent, speciality chemical, or intermediate. It is also a useful scaffold for the synthesis of complex compounds. The compound has been shown to be useful in research and industry due to its high quality and versatility. 1-(2-(4-(Chloromethyl)phenoxy)ethyl)azepane HCl has CAS No. 223251-25-0 and can be used as a reaction component in organic synthesis reactions.</p>

<p>4-(2-Aminoanilino)pyridine is a pyridine that has been shown to be an impurity in the acid salt of 4-(2-aminophenyl)pyridine. It is an acidified impurity that can form when the pyridine reacts with hydrochloric acid or sulfuric acid.</p>

<p>1-(Methylsulfonyl)piperidine-4-carbohydrazide is a fine chemical that has been used as a versatile building block in the synthesis of pharmaceuticals, research chemicals, and speciality chemicals. It has been used in the synthesis of a number of complex compounds, such as for example 4-methyl-N-[(4'-methoxybenzoyl)amino]benzenesulfonamide. 1-(Methylsulfonyl)piperidine-4-carbohydrazide is also an intermediate in the synthesis of other compounds. It is a white solid with CAS No. 312515-49-4 and melting point 159°C.</p>

<p>1-Methyl-4-phenyl-piperazine (MPP) is a drug that inhibits the serine protease and blocks the activation of tyrosine kinases. It is used in diagnostic testing to identify mutations in genes encoding for serine proteases, such as trypsin, chymotrypsin, and elastase. MPP has been shown to reduce blood pressure in rats by blocking the 5-HT4 receptor. This compound also enhances mitochondrial membrane potential and emits light when it is excited by an electron beam.</p>

<p>6-Fluoropyridine-2-carbonyl chloride (6FC) is a versatile building block that is used in the synthesis of complex compounds. It is also a reagent for organic chemistry, research chemicals, and speciality chemicals. 6FC has been shown to be useful as a building block for the preparation of high quality and useful intermediates. The compound reacts with nucleophiles in good yields to produce amines, nitriles, alcohols, and carboxylic acids. 6FC can also be used as a reaction component in organic reactions. It has been shown to be an excellent scaffold for the synthesis of bioactive molecules such as amino acid derivatives and natural products.</p>

<p>6,6'-Dibromo-2,2'-bipyridine is a synthetic molecule that is used to produce amines. It can be synthesized in a cross-coupling reaction involving the reaction of an amine with bromine and a palladium catalyst. 6,6'-Dibromo-2,2'-bipyridine reacts with formaldehyde to form 2,4-diaminobiphenyls. This reaction is catalyzed by acid or base. 6,6'-Dibromo-2,2'-bipyridine has been shown to be reactive and photoexcited. Its photophysical properties make it a useful synthetic intermediate for the production of amines.</p>

<p>3-Hydroxypyridin-4(1H)-one is a compound that belongs to the group of organic compounds called pyridines. It is a colorless, crystalline solid with a melting point of 210 °C. 3-Hydroxypyridin-4(1H)-one is soluble in ether and chloroform. 3-Hydroxypyridin-4(1H)-one forms complexes with metal ions such as copper, zinc, and nickel. The stability constants for these complexes are in the order of Cu &gt; Zn &gt; Ni. Potentiometric titration experiments show that the ligands are stronger bases than water and therefore react more strongly with copper ions than hydroxide ions.</p>

<p>4-Chloro-6-hydroxypyrimidine is an organic compound that is used as a precursor to other chemical compounds. It can be prepared by the reaction of ethylene with chlorine in the presence of carbon disulphide. 4-Chloro-6-hydroxypyrimidine has been shown to react with halides, amidines, and ethylene to form tritiated pyrimidines. It also reacts with disulphides, chlorinates and uracil. 4-Chloro-6-hydroxypyrimidine is reactive and can undergo desulfurization reactions with aluminium and malonate to form chloride or sulphoxide. The halides, amidines, and ethylene are all reactive substances that can react with each other or undergo other reactions to form new substances.</p>

<p>2-Amino-6-bromopyrazine is a versatile building block that can be used in the synthesis of complex compounds. It is also used as a reagent, speciality chemical and useful scaffold for the synthesis of pharmaceuticals and other chemicals. 2-Amino-6-bromopyrazine is available from Sigma Aldrich with CAS No. 54237-53-5.</p>

<p>3-Amino-2-pyrazinecarboxylic acid (APC) is a molecule that has been studied from many different theoretical perspectives. It has been shown to have magnetic, vibrational and spectroscopic properties. APC has a molecular electrostatic potential that can be calculated by the functional theory of atoms in molecules. This theory predicts the distribution of electron density between atoms in molecules and is used to identify which parts of a molecule are more likely to react with other molecules. The Raman spectra of APC show an intense peak at 1108 cm-1 and two weak peaks at 1265 cm-1 and 1403 cm-1. The frequency of these peaks corresponds to a bond length of 1.3 Å, 1.5 Å, and 1.7 Å respectively, corresponding to π bonds in benzene rings, σ bonds and π bonds in amide groups respectively, or σ bonds in amide groups respectively.</p>

<p>1-(1-Naphthyl)piperazine hydrochloride is a 5-HT3 receptor antagonist that has been shown to act as a potent serotonergic agent in the central nervous system of mammals. It is believed to inhibit the presynaptic serotonin uptake, resulting in an increase of serotonin concentration at the postsynaptic 5-HT1A receptor cells. 1-(1-Naphthyl)piperazine hydrochloride has also been shown to be a potent 5-HT1A receptor agonist and has antinociceptive effects following administration. This drug has been found to be more selective for the peripheral nervous system than other drugs of this type. It does not cross the blood-brain barrier and therefore does not interfere with mental function or behavior.</p>

<p>2,3,3-Trimethyl-3H-benzo[e]indole is a reactive molecule that has been shown to be an effective treatment for cervical cancer. It can be used in conjunction with monoclonal antibodies that have been designed to target the acidic protonation sites on the surface of cervical cancer cells. This active form binds to the site and emits fluorescence when illuminated with a laser, which can then be detected by a confocal microscope. This technique can also be used for the diagnosis of other cancers. 2,3,3-Trimethyl-3H-benzo[e]indole is not toxic to human serum as it does not react with this type of tissue.</p>

<p>1-Pyrimidin-2-ylpiperidin-4-amine dihydrochloride is a high quality, crystalline compound with a CAS number of 1179369-48-2. It is an intermediate in the synthesis of various fine chemicals, including pharmaceuticals and pesticides. 1-Pyrimidin-2-ylpiperidin-4-amine dihydrochloride also has applications as a versatile building block for the synthesis of other compounds and is used as a reaction component in organic chemistry. This reagent can be used to synthesize many different compounds for use in research or medical purposes.</p>

<p>3-Amino-2,6-dichloropyridine is a carboxamidopyridine that is used as an antiplatelet agent. This drug inhibits the action of ADP and thrombin in platelets, thereby inhibiting platelet aggregation. 3-Amino-2,6-dichloropyridine has been shown to be effective when given orally and is not degraded by stomach acid. It has been shown to inhibit transcriptase activity in vitro. The drug also inhibits the synthesis of prostaglandin E2 (PGE2) through inhibition of cyclooxygenase (COX) enzymes and prevents platelet aggregation by suppressing the production of adenosine diphosphate (ADP).</p>

<p>The compound 3-Chloro-5-(trifluoromethyl)pyridine-2-carboxylic acid is a synthetic intermediate that has been used in the synthesis of amides with high analytical quality. It is also an important reagent for the synthesis of many pharmaceuticals and agrochemicals. In addition, 3-chloro-5-(trifluoromethyl)pyridine-2-carboxylic acid has been shown to have dose dependent phytotoxic effects and causes plant growth inhibition.</p>