Nitro

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

<p>3-Methyl-4-nitroiminoperhydro-1,3,5-oxadiazine is a synthetic chemical compound that can be used as a pressurizing agent. It is an acidic compound and has high yield. 3-Methyl-4-nitroiminoperhydro-1,3,5-oxadiazine is also used to produce formic acid and can be found in the environment as a pollutant. This chemical may be harmful to insects. 3-Methyl-4-nitroiminoperhydro-1,3,5-oxadiazine has been used in scientific research to synthesize paraformaldehyde and recycled materials from formaldehyde. This chemical is also often used as a diluent or reagent in laboratory experiments.</p>

<p>4,5-Dichloro-2-nitroaniline is a chemical compound that has been shown to be an uncoupler of oxidative phosphorylation in ciliates. It is experimentally shown that the reaction yield for 4,5-Dichloro-2-nitroaniline is much higher than that of the corresponding methylbenzene. The two isomers are not detected in the gaseous phase, but only as products of thermal decomposition at high temperatures. Linear regression analysis and predictive models were used to evaluate the transfer and population growth rates at different temperatures. Narcosis was observed in rats exposed to 4,5-Dichloro-2-nitroaniline at concentrations greater than 0.1 ppm (0.1 mg/L).</p>

<p>2,4-Difluoro-5-nitrobenzonitrile is a chemical that has been found to have affinity for the central nervous system. It inhibits the reuptake of monoamines such as dopamine and serotonin. This chemical has been shown to be endogenously produced in humans and animals. 2,4-Difluoro-5-nitrobenzonitrile also inhibits the uptake of amines by blocking the activity of their respective transporters. The compound is an isomeric mixture of two possible structures, which differ in their position on the benzene ring. The first form is characterized by a low affinity for neurotransmitter receptors and therefore has low inhibitory properties on monoamine uptake. The second form has greater affinity for neurotransmitter receptors and therefore has greater inhibitory properties on monoamine uptake, although at higher concentrations it may lead to adverse effects on muscle tissue.</p>

<p>4-Nitro-1,2,5-oxadiazol-3-amine is a molecule that has been shown to be an inhibitor of the epidermal growth factor receptor (EGFR). The optimal reaction conditions for this molecule were determined by crystallography. These results were confirmed by prognosis assays and the determination of tautomers. This molecule may be used in diagnosis and as a potential treatment for cancer. 4-Nitro-1,2,5-oxadiazol-3-amine binds to the EGFR at a site different from that of erlotinib, an inhibitor currently used in the clinic. This binding leads to inhibition of protein synthesis and cell division by preventing the activation of downstream signal transduction pathways. The molecule also inhibits tumor cell proliferation and induces apoptosis by preventing the production of nitric oxide (NO) and reactive oxygen species (ROS).</p>

2-Chloro-4-nitro-6-bromoaniline is a dispersive, linear range, ammonolysis and chloride free oxidant for wastewater treatment. This compound is effective at removing organic pollutants from wastewater and has been shown to be both environmentally safe and cost effective. 2-Chloro-4-nitro-6-bromoaniline is also used as a polymerization initiator in the production of polyester resins. It can be manufactured by recycling anilines by reacting them with bromine in the presence of an acid catalyst. 2CNBBA is used as a hydrogen bond acceptor in microextraction of chlorinated compounds from water samples.

<p>3-Bromo-2-nitrophenol (3-BNP) is a brominating agent that can be used in the synthesis of a variety of compounds. It is prepared by the refluxing of 3-bromo-2-nitrobenzene with lithium chloride, followed by treatment with trifluoromethanesulfonic anhydride to yield 3-bromo-2-(trifluoromethyl)phenoxyacetic acid. The product can also be obtained from 2,4,6-trinitrophenol and NBS. 3-BNP has shown chemoselectivity for chlorides relative to iodides or fluorides. The yields are higher when it is used in coupling reactions and permutations with lithium or magnesium.</p>

<p>Please enquire for more information about 4-(4-Nitrophenoxy)butanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (2E)-3-(Dimethylamino)-1-(3-nitrophenyl)prop-2-en-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl3-formyl-4-nitrobenzoate is a polycyclic, boronic ester ligand that can be used in organic synthesis. It has a monocyclic alkenyl group with substitutable hydrogens and a haloalkyl substituent. The heterocycle is an aryloxy substituted with an alkynyl group. This reagent has been patented by the University of California.</p>

1-[(4-Nitrophenyl)methyl]-1H-1,2,4-triazole (NPT) is a drug that is used to treat migraine. It is an effective and fast acting drug that has been shown to be more efficient than other triptans. NPT inhibits the uptake of serotonin by binding to its receptors in the brain and causing vasoconstriction. The compound has been found to be safe for use in humans. However, it may cause impurities such as genotoxic nitro groups which are harmful to cells if present at high concentrations. There are various techniques that can be used to measure the kinetics of NPT and determine whether it has been hydrogenated during synthesis or not. These include calibration curves, HPLC, and GC methods.

<p>2,6-Dichloro-5-nitropyrimidin-4-amine is a chlorinating agent that reacts with aliphatic and aromatic amines to form substituted pyrimidines. The substitution pattern of the product depends on the regioselectivity of the reaction. 2,6-Dichloro-5-nitropyrimidin-4-amine is one of the few chlorinating agents that react with propylamine. Substitution at position 2 of the purine ring has been found to be more selective than substitution at position 6. The 2,6-dichloropyrimidine can also be used as a nitro group source in chemical synthesis or as an intermediate in production of other compounds.</p>

6-Nitro-1H-quinazoline-2,4-dione (6NQD) is a carbonyl compound and an intermolecular hydrogen bond donor. It is synthesized by nitration of 1H-quinazoline-2,4-dione with nitric acid. This product has been studied by x-ray diffraction and spectroscopy techniques. 6NQD has been found to have yields of 48% in the synthesis reaction and the average yield is 61%. The x-ray analysis technique was used to characterize the molecular structure of this product. 6NQD has shown to be centrosymmetric and exhibits intermolecular hydrogen bonding.

<p>3-Nitro-benzene-1,2-diol is an inhibitor of catechol-o-methyltransferase (COMT), which catalyzes the transfer of a methyl group from S-adenosyl methionine to dopamine. This results in the formation of 3-O-(methylamino) catechol. COMT inhibitors are used as pharmaceutical preparations for the treatment of Parkinson's disease and other diseases involving dopamine. 3-Nitro-benzene-1,2-diol has been shown to inhibit COMT and prevent the breakdown of dopamine in the brain, which may be beneficial for treating Parkinson's disease and other nervous system diseases.</p>

<p>1,8-Dinitropyrene is a genotoxic and mutagenic potential agent. It has been shown to induce nitric oxide synthase activity in rat liver microsomes, which may be due to its ability to activate the redox potential of the cells. 1,8-Dinitropyrene also induces enzyme activities such as p450 and nitroreductase in rat liver microsomes. This chemical has an analytical detection limit of 0.05 ppm and can be used as a marker for environmental exposure. 1,8-Dinitropyrene is genotoxic and carcinogenic in rats but not mice. It has been shown to induce mutations at the thymidine position of calf-thymus DNA and is potent inducer of genetic mutation in vitro.</p>

<p>4-Nitrobenzyl bromide is a reactive compound that reacts with the hydroxyl group of phenols to form 4-nitrophenols. It has been shown to react with congestive heart failure (CHF) patients' sera and bind to receptors on the surface of red blood cells, thereby inhibiting their ability to carry oxygen. The reaction mechanism for this process is unclear, but it is thought that it may involve a nucleophilic attack on the double bond in the phenol by a hydroxyl radical. This chemical can also be used as an analytical method for determining organic acids in natural compounds. Monoclonal antibodies are used for this purpose because they are specific for certain organic acids and thus will only react with them.</p>

<p>3-Nitro-4-chloro-benzotrifluoride is a nucleophilic reagent that reacts with aryl chlorides, such as phenoxazine and chloride, to give the corresponding nitro compounds. The reaction yield is dependent on the solvent, with higher yields obtained in n-dimethyl formamide than in dichloromethane. 3-Nitro-4-chloro-benzotrifluoride has been investigated for its potential use in cancer therapy. It inhibits the proliferation of a number of cancer cells, including resistant mutants. The deuterium isotope effect has also been used to determine the mechanism of action of 3-nitro-4-chloro benzo trifluoride.</p>

Please enquire for more information about 1-(2-Amino-5-nitrophenyl)ethanone including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>2-Methyl-3,5-dinitrobenzonitrile is a nitro compound that is used as a coccidiostat in the poultry industry. It inhibits the development of coccidiosis in chickens by preventing the growth of protozoa. 2-Methyl-3,5-dinitrobenzonitrile binds to DNA and RNA and prevents protein synthesis, thereby inhibiting cell division and causing death. This drug has been shown to be an analog of benzene, hexane, and pyridine. The structural analysis of this molecule reveals that it contains two nitro groups attached to a benzene ring. One nitro group is located on each methyl group. The hydrogen atoms are replaced by fluorine atoms with one hydrogen atom being replaced by chloride atom. The other nitro group is located on the 3rd carbon on the right side of the benzene ring. This molecule also contains three chlorine atoms which are attached to two adjacent carbons</p>

<p>3-Nitrobenzanilide is an intermediate in the synthesis of a number of pharmaceuticals and pesticides. It is used as an activated reagent to introduce the benzoyl group by reaction with dimethylformamide. 3-Nitrobenzanilide can be prepared from phenylacetonitrile, benzoyl chloride, and ammonia or from nitrobenzene and sodium cyanide. The nature of the nitro group on the benzene ring determines whether the product is a diazo compound or a carbonyl compound. 3-Nitrobenzanilide has been shown to have plant disease control properties via its ability to inhibit plant enzymes such as acetylcholine esterase.</p>