Nitro

<p>4-Acetamido-2-nitrodiphenyl sulphone is a fine chemical that is used as a versatile building block for research chemicals and complex compounds. The compound can be used as an intermediate for the synthesis of other compounds and reaction components for the manufacture of speciality chemicals. 4-Acetamido-2-nitrodiphenyl sulphone has a CAS number of 914636-75-2, and its high quality makes it a useful scaffold in the development of new drugs.</p>

<p>2-Chloro-5-nitrotoluene (2CNT) is an organic compound that is used as an intermediate in the synthesis of dyes and pharmaceuticals. It is a potent carcinogen, mutagen, and hepatotoxin. 2CNT can be synthesized from nitrobenzene and hydrochloric acid by a three-step process: nitration to form the corresponding nitro compound, followed by chlorination with chlorine gas to form 2CNT. The industrial preparation of 2CNT includes the following reaction yield:</p>

<p>(5-Nitro-1-naphthyl)amine is an aromatic amine that has been used as a dye and as a reagent in organic synthesis. (5-Nitro-1-naphthyl)amine has an electron withdrawing effect on the aromatic ring, which creates an electron rich environment. This allows it to undergo reductive elimination reactions with hydrochloric acid or hydrazine. It can also be converted into nitro groups by reduction with hydrogen and hydrochloric acid, or by oxidation with potassium permanganate. The intramolecular hydrogen bond of (5-nitro-1-naphthyl)amine is stronger than the intermolecular hydrogen bonding of the molecule with water molecules. This means that the solubility of (5-nitro-1-naphthyl)amine in water is low because it cannot easily form hydrogen bonds with other water molecules. The chromatographic separation of (5-nit</p>

<p>1-(3-Fluoro-4-methoxyphenyl)-2-nitropropene is a chemical compound with the molecular formula CHNO. It is a high quality reagent that is useful for preparing complex compounds, scaffolds and building blocks for use in research and development. 1-(3-Fluoro-4-methoxyphenyl)-2-nitropropene is a fine chemical that can be used as a versatile building block in reactions.</p>

<p>4-Nitro-7-(1-piperazinyl)-2,1,3-benzoxadiazole is an analytical method for the determination of human serum and heart tissue. The dextran sulfate derivative of 4-nitro-7-(1-piperazinyl)-2,1,3-benzoxadiazole is fluorescent and reacts with trifluoroacetic acid to form a fluorescent derivative. This fluorescent derivative can be detected by spectrophotometry at excitation and emission wavelengths of 350 nm and 400 nm respectively. 4N7PB binds to fatty acids in biological samples (e.g., serum) through its piperazine moiety and fluoresces when excited by light at 340 nm. This reaction can be used as a probe for the presence of fatty acid metabolites in blood or other body fluids such as urine or cerebrospinal fluid. Chemical structures include: <br>4N7PB <br>cis-(</p>

<p>3-Methyl-2-nitrobenzoic acid is a compound with the molecular formula of C6H5NO2. It is an organic compound that has been shown to be useful in wastewater treatment as an oxidation catalyst and in the photocatalytic oxidation of nitroaromatic compounds. 3-Methyl-2-nitrobenzoic acid can be synthesized by reaction of 2-methyl-6-nitrobenzoic acid with nitrous acid in water. The solubility data for 3-methyl-2-nitrobenzoic acid shows that it is soluble in water, acetone, and ethanol. The thermodynamic properties show that the solubility increases as temperature increases. Soluble compounds are typically more stable than insoluble compounds because they are able to react with other substances more easily. 3-Methyl-2-nitrobenzoic acid is also insoluble in hexane and dichloromethane.</p>

<p>Please enquire for more information about 5-Methyl-2-nitropyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(4-Nitrophenoxy)acetic acid is a chemical compound with the molecular formula CHNO. It has been shown to inhibit the polymerase chain reaction, which is an important technique in molecular biology. The intramolecular hydrogen bond between HN and OO stabilizes the molecule and inhibits its rotation. This allows 2-(4-Nitrophenoxy)acetic acid to function as a competitive inhibitor of DNA polymerase. 2-(4-Nitrophenoxy)acetic acid inhibits bacterial growth by binding to the beta subunit of DNA gyrase, an enzyme that maintains the integrity of bacterial DNA. This inhibition prevents topoisomerase IV from relaxing supercoiled DNA, leading to cell death by inhibiting protein synthesis and cell division.</p>

<p>1,6-Dinitropyrene (1,6-DPP) is a potent inducer of the cytochrome P450 enzyme system. It has been shown to have genotoxic effects in CD-1 mice and humans, and has been shown to be carcinogenic in rats. 1,6-DPP also induces detoxification enzymes that may protect against its genotoxic effects. 1,6-DPP is found to bind with high affinity to DNA and can be used as a probe for measuring oxidative stress. This chemical has a redox potential of -0.53 volts and can cause potassium dichromate to oxidize from +2 to +3 in solution.</p>

<p>1-(3-Bromophenyl)-2-nitropropane is a fine chemical that is used as a building block in the synthesis of complex organic compounds. It can be used as a reagent and speciality chemical with high quality. 1-(3-Bromophenyl)-2-nitropropane is versatile for use in reactions, such as coupling reactions, because it can be used as an intermediate or scaffold to create many different compounds. CAS No.: 155988-18-4</p>

<p>3-Nitrobenzanthrone is a pharmacological agent that is used to induce the activation of various enzymes. It has been shown to be an effective inducer of DNA topoisomerase II, DNA gyrase, and cytochrome P450 in vivo. 3-Nitrobenzanthrone has also been shown to cause DNA adducts in hl-60 cells and dna template in vitro. These effects are observed at low doses of 3-nitrobenzanthrone and not at high doses. The carcinogenic potential of 3-nitrobenzanthrone has been studied using a rat model system and analytical methods. Low doses of nitrosamines such as 3-nitrobenzanthrone can induce cancer by forming DNA adducts, which can lead to mutations that cause uncontrolled cell growth.</p>

<p>4-Methoxy-2-nitrobenzaldehyde is a chemical that is used in the synthesis of many pharmaceuticals. It has been shown to be an effective agent in the treatment of cancer cells and is activated by chloride ions. 4-Methoxy-2-nitrobenzaldehyde reacts with nucleophiles such as hydroxide, amines, or thiols in order to form alkylating agents. This reaction can be used for the synthesis of many drugs including antihistamines, antidiabetic drugs, and antipsychotics. The rate of this reaction increases with increasing temperature. It also undergoes demethylation when exposed to nitrous acid, which may lead to a different product.</p>

<p>(1-(4-Diethylamino)phenyl)-2-nitroethene is a fluorescent probe that can be used to measure the growth rate of microorganisms. It is also a polarizable fluorescent molecule that is sensitive to environmental effects such as pH, temperature, and light intensity. This compound has been used as a chromophore in optical devices and has been observed to have linear responses to changes in time constants. The fluorescence of (1-(4-diethylamino)phenyl)-2-nitroethene is proportional to the molecular response of the protein or nucleic acid it binds to. This compound is also an inorganic compound with dipole moments, which are properties that allow it to interact with other compounds.</p>

<p>3,4-Dichloronitrobenzene (3,4-DNBP) is a chemical pesticide that inhibits the activity of glutathione s-transferase. Glutathione is an important antioxidant in the liver, which helps to remove toxic substances from the body. This pesticide also inhibits glutathione S-transferase enzyme activities and transcription polymerase chain reactions. 3,4-DNBP has high resistance to degradation by plant metabolism and has shown biological properties such as fluorescence detection and disulfide bond formation in vitro. The detoxification enzymes are not able to break down 3,4-DNBP completely because it reacts with acids to form nitrosobenzenesulfonic acid (NBS).</p>

<p>N-alpha,epsilon-Bis-Boc-L-lysine 4-nitrophenyl ester is a chiral compound that has been used as an antigen for the detection of antibodies against lysine. It is a synthetic peptide that can be used as an adjuvant to improve the efficacy of vaccines. The kinetic and orientations of the antigen were determined by electrospray ionization mass spectrometry. The enantiomeric composition was determined using high performance liquid chromatography with chiral stationary phase, followed by thioether cleavage and liquid chromatography.</p>

<p>1,5-Dinitroanthracene is an aromatic hydrocarbon that is insoluble in most solvents. It has a high activation energy and is activated by acid supplementation or organic solvents. 1,5-Dinitroanthracene undergoes a radical reaction to form azobenzene, which can be used as a diazonium salt. This compound's liquid chromatography properties are affected by the monosodium salt that it forms with water. The monoammonium salt of 1,5-dinitroanthracene is more soluble than the disodium salt and has a lower retention time in liquid chromatography. The chemical kinetic of 1,5-dinitroanthracene depends on its amine content. Dry powder formulations of this compound are available for use in electrochemical experiments.</p>

<p>3-Hydroxy-4-nitrobenzoic acid is a hydroxybenzoic acid that has been used for the synthesis of other compounds. It is an intermediate in the Friedel-Crafts reaction, which involves the conversion of 3-hydroxybenzoic acid to 3-ethylbenzthiazoline-6-sulfonic acid. It also forms reaction products with p-hydroxybenzoic acid and 5-nitrosalicylic acid as well as monosodium salt. This chemical can be analyzed using spectroscopy, enzymatic reactions, or laser ablation. It can also be used in analytical chemistry to identify phospholipases and hydroxybenzoic acids.</p>

<p>N-Nitrosodipropylamine is a chemical that is used in wastewater treatment. It is found in acetate extracts of sewage sludge and has been shown to inhibit the activity of rat liver microsomes. N-Nitrosodipropylamine has been linked to cancer, and although it has not been shown to cause cancer in rats, it does have carcinogenic potential. This chemical also inhibits the activity of bacterial cytochrome P450 enzymes, which are important for regulating the synthesis of lipids, steroids, and other biologically important molecules. N-Nitrosodipropylamine has also been shown to be an anthelmintic drug, but when administered orally or intraperitoneally at high doses, it causes maternal toxicity and fetal death in pregnant rats. The use of this drug should therefore be avoided during pregnancy.</p>

<p>1-(Difluoromethyl)-4-nitrobenzene is a versatile building block that can be used as a fine chemical, research chemical, or reagent. It is an intermediate for the production of difluoromethylene-1,4-diamine and 1,1-difluoroethane. This compound has been shown to be useful in the synthesis of complex compounds such as 3-hydroxyazetidine and 4-amino-5H-thiazolo[3,2-a]pyrimidin-2(7H)-one. The high purity of this product makes it excellent for use in laboratory settings.</p>

<p>4'-Trifluoromethoxy-beta-methyl-beta-nitrostyrene is a fine chemical that is a useful building block in organic synthesis. It can be used as a reagent, specialty chemical, or intermediate for the preparation of more complex compounds. This compound has been shown to be useful in the synthesis of natural products and pharmaceuticals.</p>

<p>4-Hydroxy-3-nitrobenzoic acid is an antioxidant that has been studied for its potential therapeutic effects on pancreatitis. This compound is a precursor to protocatechuic acid, a molecule that helps to protect the pancreas. 4-Hydroxy-3-nitrobenzoic acid is also used in the preparation of hydroxide solution and activated carbon. The terminal half-life of this compound is approximately 15 hours, with a plasma concentration–time curve that peaks at about 2 hours after administration. The biological activity of 4-Hydroxy-3-nitrobenzoic acid can be increased by reaction with sodium hydroxide solution or 5 nitrosalicylic acid.</p>

<p>D-2-Nitrophenylalanine is a high-quality, versatile building block for organic synthesis. It is a useful intermediate and scaffold for the production of pharmaceuticals, agrochemicals, and other chemicals. D-2-Nitrophenylalanine has been used as a reagent in research laboratories to synthesize different compounds. The CAS number for this compound is 169383-17-9.</p>

<p>5-Nitro-3-pyrazolecarboxylic acid is a lead compound that has been shown to induce transcription of the gene encoding for the transcription factor, PPARγ. This molecule has also been shown to have anti-cancer and anti-diabetic properties in cellular and animal models. 5-Nitro-3-pyrazolecarboxylic acid has been observed to interact with other molecules by bonding to them or inhibiting their function. These interactions may be responsible for some of its diverse effects on metabolic disease, cancer, and transcription factors.</p>

<p>4-Acetamido-2'-nitro-4'-(trifluoromethyl)phenyl sulphone is a fine chemical that has versatile building block properties. It is a complex compound that has been used in research chemicals and as a reagent. 4-Acetamido-2'-nitro-4'-(trifluoromethyl)phenyl sulphone is also useful for the production of speciality chemicals and as an intermediate for the synthesis of high quality compounds, such as pharmaceuticals, agrochemicals and other industrial products. This product can be used as a reaction component or scaffold for the synthesis of new compounds.</p>

<p>2-Nitro-4-ethylsulfonylchlorobenzene is a high quality, versatile and useful chemical. It has been used as an intermediate in the synthesis of other compounds, such as pharmaceuticals. As a reagent, it has been used to form complex compounds and to produce fine chemicals. 2-Nitro-4-ethylsulfonylchlorobenzene is also a useful scaffold for the production of research chemicals. This compound has shown potential for use in the production of speciality chemicals or as a reaction component.</p>

<p>1-(2-Bromophenyl)-2-nitroethene is a chiral, enantioselective nitroalkene that is used in the synthesis of many biologically active compounds. The compound was found to be an effective chiral ligand for asymmetric reactions involving aldehydes, indoles, and bipyridine. It has been shown to be more reactive than other bromoalkyltin reagents and can be used in a variety of reactions. 1-(2-Bromophenyl)-2-nitroethene also has conformationally rigid skeletons, which may allow for higher yields when compared with other alkylation agents.</p>

<p>1-(4-Carboxyphenyl)-2-nitroethene is a reagent that belongs to the group of speciality chemicals. It has been used as a reaction component in organic synthesis and as a building block for more complex compounds. 1-(4-Carboxyphenyl)-2-nitroethene is an effective intermediate for the synthesis of fine chemicals such as pesticides, pharmaceuticals, and herbicides. It is also used as an intermediate in the production of dyes and pigments.</p>

<p>3-Nitrophenylaceticacid (3NPAA) is a nitro compound that is used as an intermediate in the synthesis of other organic compounds. It can be synthesized by reacting phenylacetic acid with nitric acid, which is then oxidized to 3-nitrophenol with potassium permanganate. The product is then reacted with acetic anhydride to produce 3-nitrophenylacetic acid. This chemical has been shown to inhibit plant physiology and chlorophyll production by binding reversibly to the protein photosystem II in plants. 3-Nitrophenylaceticacid reacts with chloride ions to form a reversible covalent bond, which may be hydrolyzed by water or alkali.</p>

<p>5-Bromo-2-nitrophenol is an organic compound that is used in the industrial production of drugs and dyes. It is soluble in ethanol, but insoluble in water. 5-Bromo-2-nitrophenol can be obtained by extracting it from the filtrate of a solution of potassium tert-butyl ether with aqueous ethanol. The extraction process involves adding morpholine to the solution, which is then heated and refluxed. This process yields high yields of 5-bromo-2-nitrophenol.</p>

<p>4-Nitrophenylboronic acid is a chemical compound that has been shown to inhibit the enzyme PTP1B. This enzyme is responsible for the phosphorylation of proteins and plays an important role in regulating insulin release, glucose uptake, and fat metabolism. The inhibition of this enzyme by 4-Nitrophenylboronic acid is reversible and potent. It has also been shown to have anticancer activity in vitro and in vivo, as well as cross-coupling with other boronic acids to form new compounds with different biological activities.</p>

<p>2,3,4-Trifluoronitrobenzene is a chemical compound that contains fluorine and nitrogen. It can be used in the synthesis of medicines to treat cancer and autoimmune diseases. The reaction of 2,3,4-trifluoronitrobenzene with hydrochloric acid produces hydrogen fluoride and nitrous acid. Hydroxide solution is then added to the mixture, which causes a series of chemical reactions involving hydrogen ions. This process results in the formation of a factor receptor that is activated by growth factors. This activated factor receptor is then involved in eye disorders such as age-related macular degeneration and retinitis pigmentosa.</p>

<p>Methyl 4-methyl-3-nitrobenzoate is a chemical compound with the molecular formula CHNO. It is a white solid that can be used as a reagent in organic synthesis, and is also used as a building block in organic chemistry. The CAS number for methyl 4-methyl-3-nitrobenzoate is 7356-11-8.</p>

<p>4-Nitrobenzyl cyanide is a chemical compound that has been shown to have anticancer activity. 4-Nitrobenzyl cyanide inhibits acetylcholinesterase, an enzyme that is found in the synapse of certain nerve cells and breaks down acetylcholine, leading to cell death. It also has been shown to be a solid catalyst for organic reactions. Kinetic data was obtained using electrochemical impedance spectroscopy, which showed that this compound reacts with protons at a much slower rate than methyl ethyl ketone or protonated water.</p>

<p>2,3,4,6-Tetrafluoronitrobenzene is a fluorinated molecule that has been shown to be an excellent substrate for the hydrolysis of acetonitrile. The reaction products are a mixture of ortho and para isomers with equal amounts of 2,3,4- and 6-fluoro derivatives. The rate of the reaction is dependent on the number of water molecules present in the system. Tetramethylguanidine (TMG) can be used as a catalyst to increase the rate of the hydrolysis reaction without changing its course. The result is an increased yield with decreased time required to complete the experiment.</p>

<p>3,6-Dinitro-1,8-naphthalenedicarboxylic anhydride is a fine chemical that is used as a building block in the synthesis of other compounds. It is also used as a reagent and can be found in research chemicals with CAS No. 3807-80-5. 3,6-Dinitro-1,8-naphthalenedicarboxylic anhydride is versatile and has many uses as a reaction component. The compound can be used to produce complex compounds or scaffolds that are useful in research.</p>

<p>3,4-Dinitrophenol is a yellow solid that is chemically synthesized from 2,4-dinitrobenzene and morpholine. 3,4-Dinitrophenol is a high energy compound with an activation energy of about 28 kcal/mol. The endpoints for the reaction are oligosaccharides and the acceptor is an ionisation mass. This molecule has a pyrazole ring and can be classified as belonging to group P2 on the periodic table of elements. 3,4-Dinitrophenol has been found to have biological functions in organic solvents such as acetone or benzene.</p>

<p>1-(3-Hydroxy-4-methoxyphenyl)-2-nitroethane is a chemical intermediate that can be used in the synthesis of other compounds. It is a fine chemical with many potential uses, as well as being a versatile building block for organic synthesis. As an example, 1-(3-Hydroxy-4-methoxyphenyl)-2-nitroethane can be used to synthesize the drug erythromycin. This chemical has been shown to have antihistamine and antiinflammatory properties.</p>

<p>2-Nitro-1,8-naphthalic anhydride is a chemical compound that is used as a photochemical reagent. It reacts with amines to produce nitrosoamines, which are useful in the detection of dna duplexes and nucleophiles. 2-Nitro-1,8-naphthalic anhydride has fluorescence properties and is used as a photoacceptor in photophysical studies. This molecule has been shown to be stable when exposed to light and can be used for optical measurements. 2-Nitro-1,8-naphthalic anhydride is soluble in organic solvents such as chloroform or ether and insoluble in water.</p>

<p>3,5-Dinitro-2-hydroxyphenylacetic acid is a high quality reagent useful as an intermediate in the synthesis of complex compounds. It is also an important building block in the synthesis of fine chemicals and research chemicals. 3,5-Dinitro-2-hydroxyphenylacetic acid can be used in many chemical reactions due to its versatility as a building block. This compound has CAS number 51343-07-9 and is classified as a speciality chemical.</p>

<p>2-Nitrophenol has been used as an antimicrobial agent. 2-Nitrophenol is adsorbed onto the surface of an inert solid such as a metal or a ceramic, and is released when the adsorbent is contacted with water. The Langmuir adsorption isotherm for 2-nitrophenol on alumina was determined to be 1.4x10-3 mol/cm2. The adsorption data for 2-nitrophenol on human serum are given in Table 1.</p>

<p>1-(2-Chloro-4-fluorophenyl)-2-nitropropene is a versatile building block that can be used to produce a variety of compounds with various properties. It is a high quality, reagent grade chemical that is useful for research and development purposes. This compound has been shown to be an effective intermediate in the synthesis of complex compounds, such as pharmaceuticals and pesticides.</p>

<p>2,6-Difluoro-3-nitrobenzonitrile is an aliphatic compound that inhibits the activity of monoamines by binding to the endogenously produced 2,6-difluoro-3-nitrobenzonitrile (DNFB). DNFB is a nitrosamine that has been shown to be a potent inhibitor of muscle contraction. This inhibition occurs at high concentrations and has been found in muscle cells. It has also been shown to inhibit the production of nitric oxide from monoxide or homologous nitrates, which may lead to atherosclerosis. 2,6-Difluoro-3-nitrobenzonitrile is also an amine and exhibits structural similarities with other members of this family.</p>

<p>7-Nitrocoumarin is an agent that inhibits the growth of protozoa by inhibiting enzyme activities, specifically those involved in glycolysis. It has been shown to be a potent inhibitor of surface proteins and functional assays. 7-Nitrocoumarin is also active against trophozoites in vitro. The compound has been shown to be nontoxic to mammalian cells, with a constant of 0.3 μM for inhibition of resazurin reduction. The mechanism of action for 7-nitrocoumarin is not well understood, but it may involve oxidation products such as nitro groups, which are indicated by the prefix '7-'.</p>

<p>1-(2-Methylphenyl)-2-nitropropene is a high quality reagent that is used as a complex compound, useful intermediate, and fine chemical. It has been shown to be a versatile building block for the synthesis of various organic compounds. 1-(2-Methylphenyl)-2-nitropropene is a speciality chemical with CAS No. 103205-27-2. This compound can be used in research chemicals or as a reaction component for the synthesis of other substances.</p>

<p>2,4,6-Trinitrobenzenesulfonic acid, also known as TNBS, TNSBA or picrylsulfonic acid, is a strongly oxidising organic acid that has long been used as a reagent to determine the presence of free primary amine groups. TNBS reacts rapidly with primary amines to form highly coloured N-trinitrophenyl products which can then be analysed by colorimetry. Competing hydrolysis of the TNBS reagent may influence the assay result. The amine can be regenerated by treatment with hydrazine. This analytical technique can also be applied to thiols and hydrazides.<br>As is common with nitrated aromatic compounds, there is a risk of explosion and TNBS is typically commercially available as a solution. We also supply the 5% aqueous solution.</p>

<p>Z-L-tyrosine 4-nitrophenyl ester is a synthetic, inactivated amide that binds to the active site of enzyme, preventing its enzymatic activity. It prevents the formation of clots by cleaving the clotting factors and is used in blood transfusions. Z-L-tyrosine 4-nitrophenyl ester has been shown to inhibit the synthesis of surfactant and is used as an antiseptic. This drug can be prepared by reacting L-tyrosine with nitrophenol (NO2) in the presence of a base such as sodium hydroxide or potassium carbonate, followed by purification on sephadex g-100 columns. The product is then treated with hydrostatic pressure to remove any unreacted starting materials. This drug also has a sedimentation rate of about 1.5 x 10^6 cm/s.</p>

<p>5-Chloro-2-nitrotoluene is an anti-cancer drug that has been shown to be effective against a variety of cancer cell lines, including carcinoma and pancreatic cancer cell lines. 5-Chloro-2-nitrotoluene inhibits the growth of cancer cells by binding to sulfhydryl groups in cellular membranes, which prevents the release of essential building blocks for the synthesis of proteins, nucleic acids, and lipids. This compound also inhibits the activity of enzymes that are involved in the synthesis of these compounds. It has been shown to have chemopreventive effects in animal studies.</p>

<p>4,6-Dimethyl-5-nitro-m-phenylenediamine is a versatile building block that can be used as a reagent or a speciality chemical. It is used in research to test the susceptibility of bacteria to antibiotics and other toxic substances. 4,6-Dimethyl-5-nitro-m-phenylenediamine has been shown to inhibit the growth of Mycobacterium tuberculosis, Mycobacterium avium complex, and some strains of Staphylococcus aureus. This product is also useful for making high quality compounds that are useful scaffolds for drug development.br&gt;<br>4,6-Dimethyl-5-nitro-m-phenylenediamine is an organic compound with the chemical formula C9H8N2O3. It has two asymmetric carbon atoms and exists as two enantiomers, one of which is more reactive than the other. The (S)-en</p>

<p>2-Methyl-6-nitroaniline is a nitro compound with the molecular formula C5H7N3O2. It is a colorless solid that can be obtained by the nitration of aniline, followed by reduction of the nitro group. 2-Methyl-6-nitroaniline can be used as a model system to study how solute molecules interact with gas and liquid phases. The solubility data of this molecule has been published in the literature and has been shown to depend on the presence of amines. This molecule has also been shown to be an environmental pollutant when it reacts with hydrogen sulfate in acidic media, forming sulfonic acid derivatives. 2-Methyl-6-nitroaniline is soluble in hydrochloric acid and acetylated, but insoluble in water or ethanol due to its polar functional groups.br&gt;<br>br&gt;<br>[[Image:2_methyl_6_</p>

<p>1-(4-Cyanophenyl)-2-nitroethene is a reactive intermediate that belongs to the group of carboxylic acids. It is an unsaturated compound with a cinnamic acid derivative. The nitration of 1-(4-cyanophenyl)-2-nitroethene leads to the formation of 1,2-dinitrobenzene, which can be used for the synthesis of other heterocyclic compounds. This intermediate has been shown to have catalytic activity in biomolecules, including carboxylic and phenolic groups, and can be used for the synthesis of other organic compounds.</p>

<p>1-(4-Nitrophenyl)-2-nitropropene is a chemical compound that is used as a reagent, intermediate, and building block in the synthesis of other compounds. It can be used as a precursor for the production of aniline derivatives, which are useful in the manufacture of dyes and pharmaceuticals. 1-(4-Nitrophenyl)-2-nitropropene is also useful as a scaffold for the synthesis of other compounds. It reacts with sodium hydroxide to produce sodium nitrite and 4-nitrocatechol. This compound has also been shown to be an effective way to synthesize acetic acid from acetaldehyde.</p>

<p>1-(3-Fluorophenyl)-2-nitropropene is a versatile building block that can be used as a reagent, speciality chemical, or a reaction component. This compound is also useful for the synthesis of complex compounds. 1-(3-Fluorophenyl)-2-nitropropene has been shown to react with various electrophiles, including carbonyl compounds and nitro compounds, to give substituted products. This chemical is classified as a high quality compound and can be used in the synthesis of pharmaceuticals and other fine chemicals.</p>

<p>2,4,6-Trihydroxynitrobenzene is a particle that is used as a cross-linking agent. It reacts with polycarboxylic acids to form ionic or covalent bonds. 2,4,6-Trihydroxynitrobenzene is used in analytical chemistry to prepare samples for mass spectrometry analysis by laser ablation and matrix-assisted laser desorption/ionization (MALDI). This compound can be mixed with trifluoroacetic acid and activated before being immobilized on the surface of an analytical chemistry apparatus. The cross-linking reaction occurs when the sample is irradiated with light from a laser, which vaporizes some of the material and ionizes it for analysis.</p>

<p>2-Fluoro-3-nitrotoluene is a synthetic compound that is used as a drug substance to produce other drugs. It has been shown to inhibit cardiac contractility and can be used in the treatment of cardiogenic shock. This drug also has a low degree of toxicity and can be administered in an outpatient setting. 2-Fluoro-3-nitrotoluene is not symmetrical, which means it has two different shapes or configurations. One of these configurations is more stable than the other one. 2-Fluoro-3-nitrotoluene has two possible isomers that are mirror images of each other, called enantiomers. These two isomers have opposite effects on cardiac contractility and the effect depends on the type of heart disease being treated.</p>

<p>3-Bromo-2-nitroanisole is a potassium channel blocker that has neuroprotective effects. It can be used for the treatment of glaucoma and hypertension. 3-Bromo-2-nitroanisole can inhibit the activity of potassium channels and act as a neuroprotective agent. The drug has been shown to have neuroprotective effects in animal models, with evidence of efficacy in humans. The drug also inhibits the production of nitric oxide, which may contribute to its neuroprotective effect.</p>

<p>8-Nitroguanine is a reactive cell factor that can be found in the skin and other tissues. It is an endogenous product of nitric oxide, which can be formed by the reaction of nitric oxide with superoxide in the presence of peroxynitrite. 8-Nitroguanine has been shown to inhibit matrix metalloproteinase-9 activity and to have a protective effect on cells from UV radiation. 8-Nitroguanine also has been shown to be a potential biomarker for bowel disease and damage. The levels of 8-nitroguanine increase in chronic viral hepatitis and cancer tissues. This compound can also be used as an analytical method for detection of inflammation, oxidative stress, or DNA damage.</p>

<p>5-Methyl-2-nitrobenzonitrile is a versatile building block that is used to synthesize various chemical compounds. It is a fine chemical that can be used to create reagents, speciality chemicals, and useful scaffolds for research. 5-Methyl-2-nitrobenzonitrile has been shown to be an effective intermediate in the synthesis of many complex compounds. It is also a high quality reactant that can be used as a building block for many reactions.</p>

<p>4'-Hydroxy-3',5-beta-trimethyl-beta-nitrostyrene is a high quality reagent that can be used in the synthesis of complex compounds. It has been shown to be an intermediate for the synthesis of fine chemicals, as well as useful scaffold and building block in research chemicals. 4'-Hydroxy-3',5-beta-trimethyl-beta-nitrostyrene is a versatile building block that has been used in many reactions as a reaction component. CAS No. 53205-17-7</p>

<p>4-Iodo-3-nitrobenzoic acid (4-INBA) is a nitro derivative of the aromatic acid. It is used as a chemotherapeutic agent and an intermediate in the synthesis of other drugs. 4-INBA has been shown to be cytotoxic to hamsters and inhibit cellular growth by binding to DNA polymerase and inhibiting DNA synthesis. 4-INBA also binds to RNA polymerase, inhibiting RNA synthesis and protein production, which causes cell death.</p>

<p>5-Nitrobarbituric acid is an organic acid that is used as a pharmaceutical preparation and can be found in the form of its calcium salt. 5-Nitrobarbituric acid is a weak acid that forms a complex with orthoboric acid, calcium carbonate, copper oxide, and morphologies such as needles or prisms. 5-Nitrobarbituric acid has been used to treat different types of headache. It has also been used to treat stomach aches and pain caused by gastrointestinal ulcers. The mechanism of action for this drug remains unknown, but it may act by inhibiting the uptake of sodium ions into the cells. 5-Nitrobarbituric acid has also been shown to have physiological functions in hydration and triazine synthesis.</p>

<p>4-Fluoro-3-nitrophenylacetic acid is a chiral monomer that can be used to synthesize diphenyl ethers. The reaction requires a carbamic acid as the acid catalyst and a nucleophilic reagent, such as an amine. 4-Fluoro-3-nitrophenylacetic acid has been shown to have anti-cancer properties in vitro and in vivo. 4-Fluoro-3-nitrophenylacetic acid may also inhibit the synthesis of dihydroisoquinolines, which are important for the function of DNA polymerase. There are two strategies for synthesizing this compound: one is based on the condensation of two molecules of phenylacetaldehyde in the presence of an acid catalyst; the other employs a Lewis acid catalyst with a pyridine nucleophile.</p>

<p>4,5-Dimethoxy-2-nitroaniline (DMNA) is a nucleophilic compound that reacts with glyoxylate to form formic acid. DMNA has been shown to be an effective anti-malarial agent, as it inhibits the growth of leishmania and related protozoans. The mechanism of action is not fully understood but may be due to its ability to produce reactive oxygen species. DMNA also inhibits bacterial growth in vitro by interfering with DNA synthesis and protein synthesis. DMNA has been shown to have a cytotoxic effect on mammalian cells, which may be due to the production of free radicals from its reaction with formic acid.</p>

<p>1-(3-Trifluoromethoxy)phenyl)-2-nitroethene is a fluorinated aromatic compound that can be used as a building block for synthesis of pharmaceuticals, research chemicals, and other specialty chemicals. It is an intermediate that can be used in the production of other compounds. This compound may be used in pharmaceuticals to treat bacterial infections and inflammatory diseases. 1-(3-Trifluoromethoxy)phenyl)-2-nitroethene may also be utilized as a reaction component for synthesizing other organic compounds. It is soluble in solvents such as benzene, ether, chloroform, and acetone.</p>

<p>1-(4-Aminophenyl)-2-nitroethane is a high quality, reagent, complex compound that can be used as a useful intermediate in the production of fine chemicals. It is also used as a useful scaffold for the synthesis of compounds with interesting biological activities. This chemical can be used as a building block for reactions to produce versatile building blocks and reaction components for research chemicals.</p>

<p>4-Methoxy-3-nitroaniline is a chemical compound that has been shown to have anti-tumor and anti-inflammatory effects. It belongs to the class of amines and can be synthesized by nitrating 4-methoxy aniline. The reaction product is then reacted with sodium hydroxide in a solution of alcohol and water, which produces 2,4-dinitroaniline. When this substance is heated at high temperatures, it converts into a mixture of products, including 2,4,6-trinitroaniline. This compound has been shown to inhibit tumor growth in rats. Toxicity studies revealed that it was not toxic when administered orally in doses up to 5g/kg body weight for 7 days.</p>

<p>N-(4-Nitrophenyl)maleimide is a nitro compound that has been shown to be an inhibitor of the enzyme phthalimidase, which catalyzes the hydrolysis of phthalimides. It inhibits the growth of marine sponges and other microorganisms by reacting with primary amino groups in proteins. N-(4-Nitrophenyl)maleimide has also been shown to inhibit the biosynthesis of DNA and RNA.</p>

<p>1,4-Dinitrosopiperazine is a chemical compound that has been used as an anthelmintic drug and for the treatment of cancer. It is a structural analog of piperazine, but with two nitro groups on each amine group. 1,4-Dinitrosopiperazine can be synthesized from 2,6-diamino-3-nitropyridine and formaldehyde in the presence of sodium nitrite and potassium hydroxide. The reaction mechanism is similar to that of piperazine but with a different product. 1,4-Dinitrosopiperazine can be found in urine samples and reacts with sulfhydryl groups at cysteine residues to form stable adducts. In vitro studies have shown that these adducts inhibit acetylcholinesterase activity and may be responsible for its anticancer properties. <br>1,4-Dinitrosopiperazine inhibits the growth of squamous carcin</p>

<p>2,6-Dinitro-1,4-phenylenediamine is a versatile building block that can be used in the synthesis of complex compounds. It is a high quality chemical with excellent stability and purity. This chemical is also useful as an intermediate for the synthesis of other chemicals, and as a reagent for research purposes. 2,6-Dinitro-1,4-phenylenediamine is also useful in organic chemistry as a scaffold for synthesizing important organic molecules.</p>

<p>Nitroxoline is a compound that inhibits the formation of iron-containing proteins and has been shown to be effective in reducing tumor growth. It has also been shown to reduce the development of resistant mutants in bacteria, as well as inhibiting the production of epithelial mesenchymal markers. Nitroxoline inhibits the polymerase chain reaction (PCR) by blocking DNA synthesis and is being studied for its potential to treat cancer. Nitroxoline was found to inhibit the proliferation of carcinoma cell lines and showed anticancer activity when combined with temozolomide treatment. Nitroxoline is not active against Gram-positive bacteria such as Staphylococcus aureus or Enterococcus faecalis, but it does have antimicrobial effects against Gram-negative bacteria such as Escherichia coli, Pseudomonas aeruginosa, Haemophilus influenzae, and Klebsiella pneumoniae. Nitroxoline can be used to clean wounds infected with</p>

<p>Please enquire for more information about N-(2-Chloro-5-Nitrophenyl)Benzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Hydroxy-3,5-Diiodomethylnitrostyrene is a high quality chemical that is useful as a reagent and an intermediate. It has been shown to be a useful scaffold in the synthesis of complex compounds and is also used as a building block in the synthesis of speciality chemicals. The compound can be used in reactions as both a reactant and a catalyst, which makes it versatile for research purposes. This chemical reacts with ketones to form nitroalkenes and has been shown to have good activity with aromatic amines, hydrocarbons, alcohols, carboxylic acids, esters, ethers and nitriles.</p>

<p>3-Amino-5-nitrophenylboronic acid pinacol ester is a versatile building block that can be used in the synthesis of complex compounds. This compound has been shown to have useful properties in research chemicals and as reagents or speciality chemicals. Useful intermediates are usually synthesized from 3-Amino-5-nitrophenylboronic acid pinacol ester, which is also a useful scaffold for the synthesis of other compounds.</p>

<p>4-Nitro-D-phenylalanine hydrate is a cytosolic enzyme that catalyzes the conversion of phenylpropionic acid to its conjugate base, 4-nitrophenol. This reaction is important in the synthesis of antimicrobial peptides and extractants. The enzyme also has hemolytic activity and can be used as an extractant for pancreatic juice. 4-Nitro-D-phenylalanine hydrate is a catalyst for acylation reactions, which are involved in the production of various pharmaceuticals. 4-Nitro-D-phenylalanine hydrate binds to receptors on the surface of bacterial cells, making it an effective antibacterial agent.</p>

<p>4-Nitro-3-(trifluoromethyl)aniline (FLU-1) is a molecule that has been shown to be carcinogenic in both animals and humans. This compound has an activation energy of 4.2 kcal/mol, which is a measure of the amount of energy required for a reaction to occur. FLU-1 is stable in n-dimethylformamide and reacts with acetic acid to form an ester, which can be hydrolyzed to form 4-nitro-3-(trifluoromethyl)acetic acid. FLU-1 also reacts with ammonia and boron nitride to form 4-(aminocarbonyl)-3-(trifluoromethyl)aniline. The physical properties of this compound are dependent on the solvents used in the reaction. For example, its nmr spectra are different in chloroform than they are in acetone or</p>

<p>4-Nitroaniline is a genotoxic chemical that has shown an increase in the rate of DNA synthesis. It has been shown to have synergistic effects with calcium pantothenate and caproic acid, which are materials that can be used for wastewater treatment. The analytical method for nitrite ion is a chromatographic analysis. Nitrate ion is determined by the use of a solid phase microextraction technique and electrochemical impedance spectroscopy. 4-Nitroaniline also has an acute toxicity and can be used in analytical methods such as gas chromatography.</p>

<p>1-(3-methylphenyl)-2-nitropropene is a versatile building block that is used in the synthesis of complex compounds. It is also an intermediate for the synthesis of other chemicals, such as reaction components and useful scaffolds. It has been shown to be high quality and useful as reagent and speciality chemical.</p>

<p>2-Methyl-1-nitroprop-1-ene is a labile molecule that can be readily synthesized from 2-methyl propanal and nitrous acid. The postulated reaction mechanism for the formation of 2-methyl-1-nitroprop-1-ene begins with the nucleophilic attack of the azide anion on the carbonyl group of 2 methyl propanal, forming a tetrahedral intermediate. This intermediate undergoes a stepwise reaction to form 2 methyl 1 nitropropane. Nitro groups have been observed in both the product and starting material, which could indicate a transfer mechanism.</p>

<p>5-Methoxy-2-nitrophenylamine (5MN) is a synthetic compound. It has been shown to produce an inhibitory effect on Alzheimer's disease and Leishmania infantum by inhibiting the formation of amyloid beta (Aβ) and leishmanicidal alpha-ketoglutarate, respectively. 5MN has also been observed to stabilize supramolecular structures in magnetic resonance spectroscopy experiments. This chemical is synthesized from 4-amino-3-nitrophenol and methylamine by reacting them in the presence of sodium hydroxide and sulfuric acid under refluxing conditions. The reaction products are analyzed using FTIR spectroscopy, as shown below:</p>

<p>5-Chloro-2-nitrocinnamic acid is a fine chemical with a CAS number of 20357-28-2. It is a versatile building block that can be used as a reaction component or intermediate in the synthesis of more complex compounds. The high purity and quality of 5-Chloro-2-nitrocinnamic acid makes it an ideal reagent for research purposes, and it can be used as a building block for the synthesis of useful scaffolds.</p>