Heterociclos con nitrógeno (N)

<p>Applications 2-Bromopyridine is a 2-halogenated pyridine used in the preparation of a variety of biologically active compounds such as antimalarial agents and beta-adrenoceptor agonist.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References LaMontagne, M.P. et al.: J. Med. Chem., 17, 519 (1974); Yoshizaki, S. et al.: Chem. Pharm. Bull., 37, 3430 (1989);<br></p>

<p>Applications s-Triazine-1,3,5-triethanol (cas# 4719-04-4) is a compound useful in organic synthesis.<br></p>

<p>Applications 2,4-Diaminopyrimidine-5-carbonitrile is used as an intermediate for the preparation of medicines and agrochemicals (1).<br>References (1) Otzen, T., et al.: J. Med. Chem., 47, 240 (2004)<br></p>

<p>Applications rac-trans-2,5-Dimethyl-3-(2-methylphenyl)-1-propylimidazolini-4-one Hydrochloride is the salt analogue of 2,5-Dimethyl-3-(2-methylphenyl)-1-propylimidazolini-4-one (D477055), an impurity of Prilocaine (Prilocaine Hydrochloride P725000). Prilocaine is a local anesthetic of the amino amide type and is often used in dentistry. Prilocaine is also often combined with lidocaine as a preparation for dermal anesthesia (lidocaine/prilocaine or EMLA) towards the treatment of conditions like paresthesia.<br>References Caliaro, G., et al.: J. Pharm. Biomed. Anal., 26, 427 (2001), Ulmeanu, S., et al.: Pharm. Res., 20, 1317 (2003)<br></p>

<p>Applications 2,6-diethylpyrazine (cas# 13067-27-1) is a useful research chemical.<br></p>

<p>Applications 2-Amino-5-pyrimidinol (cas# 143489-45-6) is a compound useful in organic synthesis.<br></p>

<p>Applications (S)-1-Pyridin-2-yl-ethylamine (cas# 27854-90-6) is a useful research chemical.<br></p>

<p>Applications 5-Aminomethyl-2-chloropyridine is a reagent that is used in the synthesis of macamides and analogs that have FAAH (fatty acid amide hydrolase) inhibitory activity.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Wu, H., et al.: Bioorg. Med. Chem., 21, 5188 (2013);<br></p>

<p>Stability Light Sensitive<br>Applications 1-[4-bromo-2-(trifluoromethyl)phenyl]-1H-1,2,3-triazole-4-carboxylic acid (cas# 1179507-09-5) is a useful research chemical.<br></p>

<p>Applications 4-(Trifluoromethyl)-3-Pyridinecarboxylic Acid is a useful synthetic intermediate. It can be used to prepare pyridine carboxamides as palm site inhibitors of HCV NS5B polymerase. It can also be used to synthesize pyrazolylcarboxanilides as Ca2+ release-activated Ca2+ (CRAC) channel inhibitors.<br>References Cheng, C., et al.: ACS Med. Chem. Lett., 1, 466 (2010); Yonetoku, Y., et al.: Bioorg. Med. Chem., 16, 9457 (2008)<br></p>

<p>Applications 4-Nitro-1H-imidazole-1-ethanol<br></p>

<p>Applications Intermediate in the production of Methotrexate<br>References Chiosis, G., et al.: Bioorg. Med. Chem., 10, 3555 (2002), Palanki, M., et al.: J. Med. Chem., 50, 4279 (2007), Zav'yalov, S., et al.: Pharm. Chem. J., 42, 51 (2008),<br></p>

<p>Applications 1H-1,2,4-triazole-3-sulfonamide (cas# 89517-96-4) is a useful research chemical.<br></p>

<p>Applications 2-Hydroxy-6-trifluoromethylpyridine<br></p>

<p>Stability Very Hygroscopic<br>Applications 4-(p-Chloro-α-phenylbenzyl)-1-piperazineethanol is used in the synthesis of antifungal triazole and imidazole derivatives. Impurity of an intermediate in the formation of Cetrizine.<br>References Rezaei, Z. et al.: Archiv. Pharm., 344, 658 (2011)<br></p>

<p>Applications 4-Aminopiperidine is a useful reactant in organic synthesis.<br>References Park, Sun Jun, et al.: Bioorg. &amp; Med. Chem. Let., 27(18), 4399-4404 (2017);Le Manach, Claire, et al.: J. of Med. Chem., 59(21), 9890-9905 (2016)<br></p>

<p>Applications 2-Amino-4,6-dimethylpyrimidine is a bioactive compound.<br>References Phan, D. C., et al.: Hoa Hoc Va Cong Nghiep Hoa Chat, 8, 30 (2001); Shen, Z., et al.: Yingyong Huagong, 37, 721 (2008)<br></p>

<p>Applications 2,4-Di-tert-butyl-6-(5-chloro-2H-benzotriazol-2-yl)phenol is a UV absorber.<br>References Moisan, J.: Eur. Polymer J., 16, 979 (1980); Nakata, H., et al.: Environ. Sci. Technol.,43, 6920 (2009)<br></p>

<p>Applications 2-Nitrosopyridine is a useful reactant in organic synthesis.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Li, Xing, et al.: J. of Org. Chem., 84(7), 4402-4412 (2019);Zhang, Jingchuan, et al.: Chem. - A Euro. J., 24(17), 4289-4293 (2018)<br></p>

<p>Applications An Intermediate in the synthesis of risperidone and iloperidone.<br></p>

<p>Applications [2-(1-methyl-1H-pyrazol-3-yl)-1H-benzimidazol-1-yl]acetic acid (cas# 1171565-50-6) is a useful research chemical.<br></p>

<p>Applications 5-Benzylthio-1H-tetrazole is used in the preparation of organosilicon compounds that have antibacterial activity.<br>References Baghershiroudi, Mahrokh. et al., J. IRAN. CHEM. SOC. 15,1279-1286(2018);<br></p>

<p>Applications 2-[1-(4-Piperonyl)piperazinyl]benzothiazole is a SR-4 agonist with moderate activity as a SR-3 antagonist.<br></p>

<p>Applications Oxazole (cas# 288-42-6) is a compound useful in organic synthesis.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>

<p>Applications 4-(2-Hydroxyethyl)piperazin-2-one (cas# 23936-04-1) is a useful research chemical.<br></p>

<p>Applications (S)-3-Aminopiperidin-2-one is used in preparation of Thiazoleurea derivatives for use as antitumor agents.<br>References Donald, E., et al.: PCT Int. Appl., (2020);<br></p>

<p>Applications Benzotriazole (BT) is an anticorrosive agent well known for its use in aircraft deicing and antifreeze fluids but also used in dishwasher detergents. Benzotriazole is antiestrogenic in vitro but not in vivo.<br>References Rollinson, G., et al.: Biotechnol. Lett., 8, 303 (1986), Cancilla, D., et al.: Environ. Toxicol. Chem., 16, 430 (1997), Beresford, N., et al.: Toxicol. Appl. Pharmacol., 162, 22 (2000), Cornell, J., et al.: Environ. Toxicol. Chem., 19, 1465 (2000), Giger, W., et al.: Environ. Sci. Technol., 40, 7186 (2006),<br></p>

<p>Applications 1-(2-Aminoethyl)pyrrolidin-2-one<br></p>

<p>Applications Anti-bacterial agent.<br>References Banfi, E., et al.: J. Chemotherapy, 5(3), 164 (1993),<br></p>

<p>Applications Allyl 4-Aminopiperdine-1-carboxylate has been used as a reactant for the preparation of 4-aminopiperdine analogs.<br>References Fernandez-Forner, D., et. al. Tetrahedron Lett., 42, 4471 (2001)<br></p>

<p>Applications 2-Mercaptopyridine N-oxide sodium salt is a bidentate complexing agent used to chelate transition metals at a pH range of 0.7-7.4. 2-Mercaptopyridine N-oxide sodium salt is also used as a selective absorptiometric reagent in the determination of palladium.<br>References Edrissi, M., et al.: J. Mater. Sci.-Mater. El., 22, 328 (2011); Edrissi, M., et al.: Microchem. J., 16, 526 (1971); Thakur, M., et al.: J. Nucl. Med., 26, 510 (1985)<br></p>

<p>Applications 2-Bromo-5-(bromomethyl)pyridine<br></p>

<p>Applications 4-(4-Chlorophenyl)-2,6-piperidinedione (cas# 84803-46-3) is a compound useful in organic synthesis.<br></p>

<p>5-Bromoindole-3-carboxaldehyde is a water molecule that has been crystallized in the form of an amide. It is a chemical substance with asymmetric synthesis and significant antifungal activity. 5-Bromoindole-3-carboxaldehyde is active against some strains of the fungus Candida albicans and has been shown to inhibit the growth of kidney cells. This molecule also binds to the neurokinin 1 receptor and is used as a probe for fluorescence studies. The efficient method for synthesizing 5-Bromoindole-3-carboxaldehyde includes using silico analysis to confirm the structure on a computer, then performing an asymmetric synthesis with an acid catalyst to produce this compound.</p>

<p>N-(2,6-Dimethylphenyl)-1-piperazineacetamide is a byproduct of solvents and stabilizers. It has been found to be a crystalline solid with a molecular weight of 233.3 g/mol. The crystal structure was determined and found to be composed of two molecules of acetamide that are connected through hydrogen bonds. N-(2,6-Dimethylphenyl)-1-piperazineacetamide is soluble in ethanol and ether, but insoluble in water. This compound interacts with other substances, such as recrystallizing or substituting acetamides.</p>

<p>2-Chloro-5-cyanopyrazine is a synthetic compound that has been shown to have anti-cancer properties. It is an acceptor molecule that has a nucleophilic character and can react with electrophiles to form covalent bonds. This compound has been shown to selectively inhibit the growth of cancer cells in vitro. The mechanism of action is not yet clear, but it may be due to its ability to induce apoptosis and arrest cell cycle progression at the G1 phase. 2-Chloro-5-cyanopyrazine also has the potential for use as an analytical reagent because of its high solubility in organic solvents. In addition, this compound can be used as a copper donor in reactions involving carboxylic acids or other nucleophiles. <br>2-Chloro-5-cyanopyrazine can be synthesized from benzene and chloropicrin in the presence of copper(II)</p>

<p>Please enquire for more information about 1-(2-Chloroethyl)-4-[3-(Trifluoromethyl)Phenyl]Piperazine Dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,6-Di-tert-butylpyridine is a proton donor that can be used in cationic polymerization. It is also used as a reagent to generate chloride and yield acidic products. 2,6-Di-tert-butylpyridine has been shown to react with pyridinium ions, forming pyridinium salts. The chemical structure of 2,6-di-tert-butylpyridine consists of a molecule with two phenyl groups and one tertiary butyl group. It is an aromatic compound that has been shown to have an expansion coefficient of 0.0183℃−1 when heated from 25°C to 100°C. FTIR spectroscopy has revealed the presence of hydrogen bonds between the nitrogen atom in the tertiary butyl group and the carbonyl group in the phenyl groups. The magnetic resonance spectrum showed that it has a paramagnetic character due to</p>

<p>3-(Trifluoromethyl)pyridine-2-sulfonamide is a fine chemical used in the synthesis of complex compounds, research chemicals, and reagents. It is also a useful building block for the synthesis of valuable chemical products such as pharmaceuticals, agrochemicals, and high-tech materials. 3-(Trifluoromethyl)pyridine-2-sulfonamide has been classified by the US Chemical Abstract Service (CAS) Number 104040-76-8. This product is available in bulk quantities that are both high quality and pure.</p>

<p>Enisamium iodide is an antiviral agent synthesized from isonicotinic acid derivatives, which is a small molecule inhibitor of viral RNA polymerase. It interferes with the replication process of various viruses by inhibiting the activity of RNA-dependent RNA polymerase, crucial for viral genome synthesis. Enisamium iodide exhibits its antiviral properties by impeding the replication of single-stranded RNA viruses, thereby mitigating viral propagation in host cells.</p>

<p>Diacylglycerol kinase inhibitor II is a transcriptional regulator that inhibits diacylglycerol kinase. This inhibitor blocks the signaling pathways for growth factor-β1 by inhibiting the enzyme phosphatidic acid phosphatase, which plays an important role in cellular proliferation and migration. Diacylglycerol Kinase Inhibitor II has also been shown to inhibit cation channels and calcium release from intracellular stores. Diacylglycerol Kinase Inhibitor II binds to both cytosolic and nuclear proteins. It has been shown to inhibit cell proliferation and induce apoptosis in breast cancer cells.</p>

<p>2-Chloro-3-nitropyridine is a nucleophilic compound that reacts with amines to form substituted amines. It can be synthesized by hydrolysis of chloroacetamide with hydrochloric acid and reacting the resulting ammonium chloride with nitrobenzene. The reactions are nucleophilic substitutions, which means it reacts at an electron rich atom such as the nitrogen in the ammonium chloride. This reaction is exothermic, meaning it releases heat, and the products are 2-chloro-3-nitropyridine and water.<br>2-Chloro-3-nitropyridine has been shown to inhibit α subunit of protein kinase C (PKCα) activity by binding to the PKCα ATP site. It also has been shown to react with proteins containing reactive sulfhydryl groups such as cysteine residues, forming sulfonamides or sulfoxides that may inhibit enzyme activity or</p>

<p>Please enquire for more information about 2-Piperazin-1-ylnicotinamide dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Hydroxyquinoline is a chemical compound that has been shown to have anticancer, anti-inflammatory, and antiviral properties. It is an inhibitor of the enzyme tyrosinase, which is required for the production of melanin. 4-Hydroxyquinoline has also been shown to suppress bowel inflammation by inhibiting the synthesis of 3-hydroxyanthranilic acid in cells. 4-Hydroxyquinoline has been found to be effective against Herpes Simplex Virus Type 1 (HSV1) in cell culture and in vitro assays. <br>4-Hydroxyquinoline's photochemical properties make it a useful precursor for the synthesis of other biologically active compounds. This chemical undergoes a reaction with trifluoroacetic acid to form diazonium salt intermediate, which then reacts with hydrogen peroxide to form an active oxygen species that damages DNA and kills cells.</p>

<p>Thiostrepton is an antibiotic that inhibits the synthesis of proteins by binding to the α subunit of the bacterial ribosome. It also has a polymerase chain reaction (PCR) amplification activity. Thiostrepton's inhibitory effect on protein synthesis is due to its ability to bind to the α subunit of the ribosome, which results in inhibition of enzyme activities and physiological function. The thiostrepton-resistant mutants have been found in skin cells and plants. The resistant mutants are mostly due to point mutations in amino acid residues on the surface of the ribosomal target site, which alters its affinity for thiostrepton. This antibiotic has been shown to be active against wild-type strains of bacteria, as well as methicillin-resistant Staphylococcus aureus (MRSA). Thiostrepton's active form is metabolized through hydroxylation and conjugation with glutathione or glucur</p>

<p>1-Boc-4-methylpiperazine is an inhibitor of the enzyme hydrolase. It has been shown to have a dose-dependent effect on inflammatory pain and can be used for the treatment of neuropathic pain. 1-Boc-4-methylpiperazine also has potent inhibitory activity against fatty acid amide hydrolase (FAAH) and fatty acid amide hydrolase (FAAH). It is orally administered and has been shown to have analgesic effects in animal studies. 1-Boc-4-methylpiperazine also inhibits the enzymatic activity of other hydrolases, such as cyclooxygenase 2 (COX2) and acetylcholinesterase (AChE), which are involved in inflammation, pain, and memory.</p>

<p>Vortioxetine is a serotonin modulator and reuptake inhibitor which appears to be much more potent on serotonin reuptake inhibition and 5-HT3 receptor antagonism than other interactions with the 5-HT receptor family. This drug binds selectively to 5-HT receptors and inhibits the activity of serotonin reuptake transporters on presynaptic neurons, thereby increasing serotonin concentrations in the brain. It is used for the treatment of major depressive disorder (MDD)and has also been shown to be effective against depression-related symptoms such as sleep disturbances, appetite disturbance, and weight change. Vortioxetine has also been demonstrated to suppress glioblastoma in both ex vivo human tissue samples and in mice. This may indicate vortioxetine signalling cascade activation supresses cancer cell division, and could constitute an effective part of a treatment regime for glioblastoma patients.</p>

<p>5-Iodoindole is an organic compound that is used as a nematicide. It has been shown to have cytostatic effects on the growth of human pathogens, juveniles, and model systems. 5-Iodoindole inhibits the production of reactive amines and pyridine in vivo. It also inhibits glutamine metabolism by competitive inhibition at the glutamate dehydrogenase enzyme. 5-Iodoindole also has hemolytic activity and is able to induce transcriptomic changes in P. aeruginosa cells.</p>

<p>The drug 4-Amino-5-chloro-2,3-dihydro-N-[1-(3-methoxypropyl)-4-piperidinyl]-7-benzofurancarboxamide (BZP) is a histamine H2 receptor antagonist. It binds to the histamine H2 receptor in the stomach and duodenum, thereby blocking stomach acid production. BZP has been shown to be effective for treating symptoms of constipation or diarrhoea caused by inflammatory bowel disease or abdominal surgery. BZP also reduces the risk of relapse after surgery but does not affect long term efficacy. This drug is not available in the United States and has significant interactions with other drugs and symptoms including constipation, bowel disease, long term efficacy, and analytical method.</p>

<p>Plant hormone; auxin; inducer of root development; used in plant rooting</p>

<p>4-Amino-2-methoxypyridine is an antiviral agent that inhibits the activity of the NS5B polymerase, a key enzyme in the replication of the hepatitis C virus. It is a potent inhibitor with a wide range of activity and can be used for treatment and prevention of infection. 4-Amino-2-methoxypyridine has been shown to inhibit replication of hepatitis C virus in cell culture. This compound is stable in vivo and can be administered orally, making it an attractive candidate for oral prophylaxis against hepatitis C. 4-Amino-2-methoxypyridine also exhibits good pharmacokinetic properties, including a low clearance rate and high volume of distribution, which makes it suitable for chronic administration.</p>

<p>4,6-Dimethyl-2-hydroxypyrimidine (DMHP) is an antibiotic drug that inhibits the activity of lipoprotein lipase. DMHP is a broad-spectrum antibiotic that has been shown to have inhibitory effects on bacterial growth in vitro assays. The chemical ionization method was used to measure the amount of DMHP in plasma samples. Results showed that DMHP levels were below the limit of detection in all samples. This suggests that DMHP does not accumulate in the body and may be metabolized quickly. Liquid chromatography with ultra violet light detection was used to analyze the chemical structure of DMHP and found it to be a mixture of two compounds: 4,6-dimethylpyrimidin-2(1H)-one and 2,4,6-trimethoxypyrimidine. The surface methodology was used to identify target tissues for toxicity studies, showing that this compound preferentially binds to liver tissue.</p>

<p>1-Phenyl-piperidine is a psychoactive compound that has been shown to have strong binding affinity for the κ-opioid receptors. It has also been shown to increase locomotor activity in mice and produce hallucinations. 1-Phenyl-piperidine has a number of biological properties including inhibition of dopamine uptake, induction of myocardial infarcts, and toxicity to the ischemic brain. It binds with high affinity to the multidrug efflux pumps such as P-glycoprotein (Pgp) and MDR1, which are responsible for removing drugs from cells. Pgp is induced by cytochrome P450 3A4 (CYP3A4) inhibitors such as ketoconazole, erythromycin, fluconazole, itraconazole, clarithromycin, telithromycin, nefazodone, and grapefruit juice.</p>

<p>6-Methoxyindole is an acetate extract of the plant 5-methoxyindole. It has been shown to be a 5-HT1A receptor agonist in animals, and has been shown to have cardiac effects in rats. 6-Methoxyindole is also used as a precursor for the synthesis of diphenylacetylindoles. 6-Methoxyindole is one of the molecules that can be recombined to form a batcho-leimgruber indole (BLI).</p>

<p>2-Amino-4,6-dichloropyrimidine is a chemical compound that can be used as an intermediate in the synthesis of other compounds. It is usually prepared by chlorinating 2-amino-pyrimidine with sodium hypochlorite. 2-Amino-4,6-dichloropyrimidine has been shown to inhibit the growth of herpes simplex virus and influenza virus when it is added to cell cultures. This compound also inhibits the replication of protonated nucleic acids by reacting with the amide group of nucleophilic amino acids in DNA or RNA. The reaction between 2-amino-4,6-dichloropyrimidine and amines gives pyridinium salts, which are useful intermediates in organic chemistry reactions.</p>

<p>Please enquire for more information about 7-Bromo-5-fluoro-1H-indole-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Indole-2-carboxylic acid ethyl ester is a synthetic compound that binds to cancer cells. It has been shown to inhibit the growth of leukemia cells and breast cancer cells in vitro. Indole-2-carboxylic acid ethyl ester inhibits the binding of collagen to cells, which may be due to its ability to bind to β-carboline alkaloids on collagen. The binding of indole-2-carboxylic acid ethyl ester with these alkaloids prevents them from binding to collagen, thereby preventing the formation of new collagen fibers. This drug also inhibits aldehyde production, which is important for DNA synthesis in cancer cells.</p>

<p>4-Chloropyrimidine is a nucleophilic compound that is synthesized by the reaction of acetone with hydrogen chloride. The proton NMR spectrum of 4-chloropyrimidine has been determined and it has been shown to be active against herpes simplex virus in clinical studies. The synthesis of this compound is accomplished using a flow system. It can be prepared from trifluoroacetic acid and carbon disulphide or from sodium hydroxide and amines. The structure of 4-chloropyrimidine was determined by X-ray crystallography. It reacts with organic compounds to form new compounds, such as fluorine, which are often toxic to humans or animals.</p>

<p>8-Bromoadenine is a nucleophile that reacts with electrophiles to form adducts. 8-Bromoadenine has been shown to induce DNA strand breaks and oxidative damage in vitro, which may be due to its ability to react with DNA bases and form intramolecular hydrogen bonds. 8-Bromoadenine has also been shown to cause inflammatory bowel disease in mice by increasing the production of proinflammatory cytokines. 8-Bromoadenine induces Toll-like receptor 4 (TLR4) signaling, which leads to enhancement of radiation response. This drug can also be used as the monosodium salt for treating cancer, although it only has a limited number of sequences that can be synthesized.</p>

<p>8-Aminoquinoline is a fluorescent probe that is used to detect the presence of nitrite ions in biological samples. It is used in electron paramagnetic resonance (EPR) experiments and can be used as a chemical inhibitor of cytochrome P450 enzymes. 8-Aminoquinoline has been shown to have minimal toxicity in animal models. It has been shown to inhibit the growth of Leishmania, an organism that causes leishmaniasis, by arresting protein synthesis at the ribosome level. The drug interactions of 8-aminoquinoline have not been well studied, but it may be necessary for patients to avoid other drugs that are metabolized by cytochrome P450 enzymes when taking this agent.</p>

<p>5-Azaindole is a heterocyclic compound that has been studied for its biological properties. It is a prodrug of trifluoroacetic acid, which can be used to treat metabolic disorders and autoimmune diseases. 5-Azaindole has also been shown to increase the expression of growth factor in cells, which may be useful in treating pain or bowel disease. This drug is metabolized by hydroxylation followed by conjugation with glucuronic acid and excretion in the urine. 5-Azaindole is also converted to an active form by enzymatic oxidation of a hydroxyl group and protonation on the nitrogen atom, as well as conversion to sorafenib (a drug used to inhibit tumor growth).</p>

<p>4-Mercaptomethyl dipicolinic acid is a polymerized, bifunctional molecule that can be used as a luminescent probe to study the structure and dynamics of proteins. It has been shown to bind to lanthanide ions and has fluorescence properties. 4-Mercaptomethyl dipicolinic acid can be synthesized by a method involving the reaction of mercaptoethanol with sodium dithiocarbamate and copper(II) sulfate in an aqueous solution. This reaction produces two molecules of 4-mercaptomethyl dipicolinic acid for every one molecule of mercaptoethanol used, which then reacts with two molecules of 2,4-dinitrophenol in an aqueous solution. The resulting product is then purified by recrystallization from hot water. The conformational properties of 4-mercaptomethyl dipicolinic acid are dependent on temperature, pH,</p>

<p>6-Chloro-2-fluoropyridine-3-boronic acid is a versatile building block for the synthesis of complex compounds, which can be used as a reagent in research or as a speciality chemical. This compound can be used as an intermediate, reaction component, or scaffold to synthesize other more complex structures. 6-Chloro-2-fluoropyridine-3-boronic acid is available in high quality and has CAS No. 1256345-66-0.</p>

<p>Please enquire for more information about Cetirizine propanediol ester dihydrochloride, mixture of regioisomers including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Methoxy-2-methylindole is an organic solvent that has been shown to have a wide range of bioactive properties. It is used in the production of acetylcholine, which is an important neurotransmitter. 5-Methoxy-2-methylindole also reacts with chloride ions, which may be an important factor when considering the life cycles and bioactive substances of this molecule. The reaction yield depends on the pH of the solution. 5-Methoxy-2-methylindole can undergo chlorination reactions to form polychlorinated derivatives, which are used as petrochemicals. This molecule also has retinoid properties and can act as a proton donor or acceptor depending on whether it is protonated or deprotonated.</p>

<p>2,2'-Bipyridine-5,5'-dicarboxylic acid is an algal metabolite that has been shown to have a glucose sensor function. It is synthesized by Chlorella and other green algae in response to light and high concentrations of glucose. This compound can be used as a linker for the immobilization of fluorescent probes or luminescent probes. It also has a catalytic subunit that can be used in oxidation reactions at low temperatures with chloride as the oxidant. 2,2'-Bipyridine-5,5'-dicarboxylic acid is chemically stable and does not react with chloride or ligands. It can also be used as an oxidation catalyst for reactions at high temperatures.</p>

<p>Selection reagent for orotidine 5'-phosphate decarboxylase mutants</p>

<p>1-Butyl-4-methylpyridinium chloride is a pyridine salt that is used for the treatment of osteoporosis. It has been shown to increase the rate of mineralization and reduce the viscosity of beta-amyloid peptide solutions. The biological activity of 1-butyl-4-methylpyridinium chloride has been demonstrated in animal studies, where it was shown to have a significant effect on calcium assays, hydrophilic interaction chromatography, and beta amyloid peptide. This drug also has pharmacokinetic properties that are similar to those of other pyridinium salts. Molecular modeling studies show that 1-butyl-4-methylpyridinium chloride binds well to calcium ions, which may be due to functional groups such as chlorides. This drug also has photocatalytic activity and can be used as a homogeneous catalyst in chromatographic science.</p>

<p>Indoline-2-carboxylic acid is a photophysical molecule with an absorption maximum at 518 nm. It has been shown to inhibit the activity of enzymes such as cyclooxygenase, lipoxygenase, and monoamine oxidases. This compound has been found to be effective in the treatment of cancer cells. Indoline-2-carboxylic acid is also used in pharmaceutical preparations, where it binds to enantiomers of other molecules and inhibits their biological activity. Indoline-2-carboxylic acid reacts with hydrochloric acid to form allyl carbonate and amide.</p>

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<p>(1-Methylpiperidin-2-yl)methanol is a gaseous organic acid that belongs to the piperazine class of compounds. It is used as an intermediate in the synthesis of various pharmaceuticals, including antipsychotics and antidepressants. (1-Methylpiperidin-2-yl)methanol has been shown to be an agonist of ganglion cells and can be used for the treatment of glaucoma. This compound also has shown to have anti-inflammatory properties, which may be due to its ability to inhibit nitric oxide production. Furthermore, (1-methylpiperidin-2-yl)methanol has been shown to inhibit 13c nuclear magnetic resonance spectroscopy with epoxides and hydroxyl groups. The reaction product is a crystalline solid with a molecular formula of C6H14O3N2, which corresponds to the molecular formula of 2-(dimethylam</p>

<p>3-Methyl-8-quinolinesulfonyl chloride (3MQSC) is a reaction product of 1,2,4-trioxane and thionyl chloride. 3MQSC is used as an intermediate in the production of l-citrulline from chloroacetic acid. It reacts with paraformaldehyde to form a solid phase synthesis catalyst. 3MQSC catalyzes the reaction between phosphorus pentachloride and chlorine to produce ethyl formate and hydrogen chloride gas. This process is industrialized for the production of ethyl formate, which is used for the manufacture of acetic acid, chlorinated solvents, polymers, and plastics. The high yield of this process makes it one of the most popular routes for producing ethyl formate. Catalysis by 3MQSC can be achieved at low temperature and pressure due to its resistance to heat and low boiling point.</p>

<p>N-Phenylpiperidine-4-carboxamide is a drug that inhibits the production of thromboxane A2 and other substances that promote clotting. It is used to treat patients with high blood pressure, as well as for the prevention of strokes and heart attacks. N-Phenylpiperidine-4-carboxamide is an analog of biphenyl and has been shown to have antiplatelet activity in humans. This drug also inhibits soluble guanylate cyclase, which prevents platelets from sticking together and forming clots. N-Phenylpiperidine-4-carboxamide is rapidly metabolized by esterases in the human body and excreted primarily in urine. The pharmacokinetic properties of this drug are not well understood but it can be synthesized using a number of different methods involving amide bonds.</p>

<p>Intermediate in the synthesis of linagliptin</p>

<p>3-Fluoropyridine-4-carboxaldehyde is a reactivator that can be used in the treatment of bladder cancer. It binds to pyridinium and oxime derivatives, which are present in proteins, to form a reactive intermediate. This intermediate reacts with aldehyde groups on hemoglobin, restoring the oxygen binding capacity of hemoglobin to levels seen in healthy individuals. 3-Fluoropyridine-4-carboxaldehyde has been shown to have anticancer activity against bladder cancer cells and also has potential use as an additive for the treatment of red blood cells.</p>

<p>4,6-Dihydroxy-2-methylpyrimidine is a monomer that is used in the synthesis of polyurethanes. It is an intermediate in the reaction between hydrochloric acid and nitrous acid, which produces 4,6-dichloro-2-methylpyrimidine. The reaction mechanism involves transfer of a methyl group from an organic molecule to hydrochloric acid. This reaction can be carried out at either low or high pH values. The addition of magnesium salt increases the rate of the reaction by increasing the solubility of chloroformate in water. When ethyl esters are used as starting materials, a constant conversion rate can be obtained with a large excess of magnesium salt.</p>

<p>7-Methoxy-1H-indole (7MI) is a synthetic compound that exhibits anti-inflammatory activity. It is an analog of the amino acid methionine found in proteins and its synthesis involves the condensation of a chlorinated alkyl acetate with an esterified hydrazide to form the corresponding amide. 7MI has been shown to inhibit both bacterial and mammalian protein synthesis, as well as to inhibit tumor cell growth. 7MI binds reversibly to the N7 atom of the adenine base in DNA, thereby inhibiting DNA replication through inhibition of DNA polymerase.</p>

<p>2,6-Pyridinediyldimethanamine is a reactive molecule that can be used in clinical studies. It has been shown to have an effect on mammalian cells, and it can also be used for structural studies of the molecule. This compound is mainly used as a chelate ligand in hydrogen bonding reactions. The kinetic of the reaction between 2,6-pyridinediyldimethanamine and chloride has been studied experimentally and found to follow second-order kinetics. X-ray crystal structures show that this compound forms a hydrogen bond with chloride ions.</p>

<p>2-Amino-3-chloro-5-(trifluoromethyl)pyridine is a versatile building block that can be used in the synthesis of complex compounds. It is a useful intermediate for synthetic organic chemistry, and can be used as a reagent or speciality chemical. This compound has shown to have high quality and is useful as a scaffold in the synthesis of research chemicals.</p>

<p>2-(Methylamino)pyridine-3-methanol is an industrial chemical that is used as a solvent and in the production of potassium sulfate. It has a high boiling point, which makes it a good choice for large-scale industrial processes. 2-(Methylamino)pyridine-3-methanol is also an organic solvent, which can be used to dissolve many other molecules. This product can be used as a conditioner or tertiary butylating agent in the production of organic compounds. Its product yield is high, with only 10 grams needed to produce 1 kilogram.</p>

<p>Catalyst; intermediate in organic syntheses</p>

<p>Pantoprazole is a proton pump inhibitor (PPI) that blocks the production of stomach acid by inhibiting the H+/K+-ATPase enzyme in gastric parietal cells. The chemical compound 3,4-Dimethoxy-2-hydroxymethylpyridine is a sodium salt of pantoprazole. It is commercially available as the anhydrous form, which is a white crystalline powder. This chemical has been used to regulate the amount of water in industrial processes and to salify materials such as lead oxide. Pantoprazole sodium chloride can be prepared by evaporating and drying with anhydrous sodium chloride or by heating an aqueous solution of pantoprazole sulfate.</p>

<p>Thiamine derivative; coenzyme of transketolase</p>

<p>4,4'-Dinonyl-2,2'-bipyridine is a high-yield transfer reagent that is used in organic synthesis. It can be used to transfer aryl or alkyl groups from ancillary to the functional group on the substrate. 4,4'-Dinonyl-2,2'-bipyridine is also used for the production of polymers and organic semiconductors. In addition, this compound has been shown to be useful in the production of silicon solar cells and as a catalyst for photovoltaic devices. 4,4'-Dinonyl-2,2'-bipyridine has been shown to be thermostable and can be used in temperatures up to 200°C. This compound is also a ligand with ruthenium complex properties and can be used as an electron acceptor in radiation therapy procedures.</p>