Nitro

<p>1-(4-Fluorophenyl)-2-nitropropene is a versatile building block that is used in the synthesis of a wide range of complex chemical compounds. This compound is also found to be useful as a key component in the synthesis of pharmaceuticals, research chemicals, and other fine chemicals. 1-(4-Fluorophenyl)-2-nitropropene can be used as a reagent for organic reactions, and it has been shown to react with amines to form nitrosoamines. This compound is an intermediate in the synthesis of 4-fluoroaniline, which has various industrial applications. The chemical formula for 1-(4-Fluorophenyl)-2-nitropropene is C8H6FO3N3O2.</p>

<p>4-Amino-2-nitrobenzoic acid is a chemical compound that can be found in human urine. It belongs to the group of amides and is an acidic substance. The pH optimum for 4-Amino-2-nitrobenzoic acid is between 1 and 2. This compound can be hydrolyzed by acidic conditions, forming an amide derivative. The uptake of 4-Amino-2-nitrobenzoic acid in humans and animals depends on the glomerular filtration rate, which influences how much of the compound will be excreted by the kidneys. The uptake also depends on the acetylation status of the compound, which is determined by its metabolism with phosphatase enzymes. Organic acids are also present in human urine, which may result in the formation of 4-Amino-2-nitrobenzoic acid as well as other compounds with similar structures.</p>

<p>2-Bromo-4-Chloro-1-Nitro-Benzene is a paraoxon compound that is used to produce chemical weapons. It has been shown to be able to neutralize nerve agent in the body and is undergoing clinical trials as an antidote for nerve agents. 2-Bromo-4-Chloro-1-Nitro-Benzene is produced by trituration from the corresponding bromide or chloride in the presence of nitric acid and hydrochloric acid and can be purified by recrystallization from water. The microreactor process was used to prepare this substance because it gave good yields, was easy to implement, and was cost effective. 2BCNB has also been shown to be a potent transport inhibitor of clozapine with configurable nature, portability, and detoxification properties.</p>

<p>2-Hydroxy-5-nitrocinnamic acid is a high quality, reagent intermediate that is used in the synthesis of complex compounds. It can be used as an important intermediate for the production of fine chemicals and speciality chemicals. 2-Hydroxy-5-nitrocinnamic acid has been shown to have versatile building block properties and can be used as a useful scaffold or building block in chemical reactions.</p>

<p>3-Methoxy-4-(4-nitrobenzyloxy)benzaldehyde is a chemical intermediate that is used in the synthesis of complex compounds. It has been shown to be an effective reagent for the synthesis of various organic compounds, such as pharmaceuticals and pesticides. 3-Methoxy-4-(4-nitrobenzyloxy)benzaldehyde is also used as a research chemical or as a speciality chemical in laboratories. This compound can be used as a building block in the synthesis of other compounds with interesting properties, such as 3-methoxy-4-(2,5-dichlorobenzyloxy)benzaldehyde.</p>

<p>2-Nitro-4,5-methylenedioxybenzaldehyde (2NMB) is a molecule with a molecular weight of 188.24, an empirical formula of C8H8NO2 and a chemical structure consisting of a benzene ring attached to two nitro groups. 2NMB has been shown to bind to the dopamine β-hydroxylase enzyme in human serum and inhibit the production of dopa, which leads to a decrease in dopamine levels. It also inhibits the growth of staphylococcus, cryptococcus neoformans, and typhimurium. 2NMB also has been used as radiotracers for gyrase activity and can be used for asymmetric synthesis due to its piperonal group. The uptake of 2NMB by cells is dependent on its nucleophilic properties.</p>

<p>Nitroxynil is an anthelmintic drug that belongs to the group of nitroimidazoles. It has a high level of resistance to parasites and is used in animals for the treatment of fasciola, trichuris, and other endoparasites. Nitroxynil is a prodrug that requires activation by hydrolysis with trifluoroacetic acid or enzymatic reduction by hydroxylases. The pharmacokinetics of nitroxynil have been studied using an analytical method based on electrochemical impedance spectroscopy (EIS). This technique measures the changes in electrical impedance as a result of chemical reactions at electrodes immersed in a solution. It has been shown that nitroxynil can be detected in plasma at concentrations of 5–50 ng/mL after intravenous administration.</p>

<p>2-Methyl-3-nitrophenylacetic acid is an alkali metal, which is obtained by the condensation of 2-methylphenol and nitric acid. The synthesis of this compound can be achieved through catalytic reduction of the nitro group with hydrogen in the presence of a nickel catalyst. This method has been shown to produce high yields. 2-Methyl-3-nitrophenylacetic acid is mildly toxic to humans and animals. It is a dopaminergic agent that has been used as a precursor for the production of ropinirole hydrochloride, which is used in the treatment of Parkinson's disease.</p>

<p>2-Chloro-5-nitroacetophenone is a synthetic chemical that is used in the synthesis of vismodegib. It has been shown to have pharmacokinetic properties, such as a low clearance and high volume of distribution. A number of impurities are found in this chemical, including halide ions, amines, and benzofuran derivatives. 2-Chloro-5-nitroacetophenone is genotoxic and can cause cancer. This chemical should not be exposed to radiation or chlorine gas.</p>

<p>4-Bromo-2-fluoro-5-nitroaniline is a chemical intermediate that has shown potential for use in research. This compound has been used as a building block for the synthesis of other compounds, and it has proven to be an excellent reagent for the reaction of amines with ketones. The CAS number for this product is 87547-06-6.</p>

<p>2-Nitrophenylacetic acid is a synthetic product that has been studied by electrochemical techniques. It is soluble in human serum and can be detected by a chromatographic method. The cationic surfactant, oxindole, chloride, and optimal reaction conditions are known for the solute. 2-Nitrophenylacetic acid is a pharmaceutical drug that can be cleaved into nitro and carboxylate products with hydrochloric acid and β-unsaturated ketone as cleavage products.</p>

<p>Ethyl 2-cyano-3-(4-nitrophenyl)prop-2-enoate is a functionalized molecule that contains a dipole. It has high selectivity for 1,3-dipolar cycloadditions because the electron density of the methylene group is greater than that of the aldehyde group. The mechanistic theory for this reaction is that the electron density on the methylene group in ethyl 2-cyano-3-(4-nitrophenyl)prop-2-enoate will cause it to become more reactive than the aldehyde group. The dipoles in this molecule are oriented such that they can react with each other to form an intermediate and then an adduct. This isomerization occurs through either dipolarophilic or electrocyclic mechanisms.</p>

<p>1-Bromo-2-nitrobenzene is a chemical compound that can be used as a palladium catalyst for the synthesis of organic compounds. It is a group P2 ligand, which means it will bind to metals such as palladium and platinum. 1-Bromo-2-nitrobenzene undergoes nucleophilic addition reactions with diazonium salts to form the corresponding diazonium bromide. The diazonium bromide can then undergo transfer reactions with other molecules, such as alcohols and amines, to form new products. 1-Bromo-2-nitrobenzene also undergoes staudinger reduction to form a ketone or an aldehyde. This reaction requires the presence of hydrochloric acid, halides, or other electron-donating compounds in order to work properly. Chemical reactions involving 1-bromo-2-nitrobenzene may include</p>

<p>5,5-Dimethyl-3-(4-nitrobenzyl)imidazolidine-2,4-dione is a versatile chemical that can be used as a building block in the synthesis of complex compounds. It is an intermediate in the production of research chemicals and is also used as a reaction component in the synthesis of speciality chemicals. 5,5-Dimethyl-3-(4-nitrobenzyl)imidazolidine-2,4-dione has been shown to have high quality properties when synthesized using high purity reagents.</p>

<p>5-Nitroisophthalic acid monomethyl ester (NIAE) is an acetylating agent that can be used for the preparation of 5-nitroisophthalic acid, which is a precursor to the synthesis of dyes and pharmaceuticals. The acetylation reaction of NIAE with proteins produces an insensitive material. Acetylation also inhibits the activity of serine proteases and virus replication. In addition, it has been found that the catalytic reduction of NIAE with palladium is faster than other synthetic methods. Optimal reaction conditions are obtained by adding chloride ions to the reaction mixture, while reductive conditions are optimal for catalysis. Reaction time can be shortened by using a soluble catalyst such as iodide ion or mercury(II) sulfate. The active site of NIAE contains a nitro group that reacts with substrates in the presence of oxygen, forming a product from which the acetyl group has been removed</p>

<p>2-Methyl-5-nitrobenzoic acid is a synthetic compound that has been shown to inhibit the growth of tumor xenografts in mice. This compound has been shown to inhibit the production of prostate-specific antigen and prostate cancer cells, as well as cause apoptosis in prostate cancer cells. 2-Methyl-5-nitrobenzoic acid also inhibits the activity of vitamin D3 and docetaxel, which are both chemotherapeutic agents used to treat prostate cancer. 2-Methyl-5-nitrobenzoic acid is a thermodynamic inhibitor with an IC50 value of 0.1 mM. It is an inhibitor of cellular respiration and mitochondrial function with a Km value of 1 mM. This agent also inhibits tumor perfusion, which may be due to its ability to induce apoptosis in tumor cells.</p>

<p>4-Hydroxy-3-nitropyridine is an organic chemical compound with the molecular formula CHNO. It has a structure that is composed of a nitro group bonded to a pyridine ring. 4-Hydroxy-3-nitropyridine can be found in wastewater and as a byproduct of the production of dyes, drugs, and explosives. It has been shown to react with primary amines to form nitrosamines. In its tautomeric form, 4-hydroxy-3-nitropyridine is more reactive and will react with chloride ions to form hydroxylamine. This reaction is used commercially for the synthesis of hydrazine and other products.</p>

<p>2-Fluoro-5-nitrobenzoic acid is a molecule that can be used in biological studies to measure the proton concentration of a solution. This compound has been shown to bind to caffeine and β-amino acids, which may be due to its ability to form intermolecular hydrogen bonds. 2-Fluoro-5-nitrobenzoic acid has also been shown to enhance reactive oxygen species generation by nitrobenzoic molecules, making it a potential drug for the treatment of cancer.</p>

<p>2-Bromo-5-nitro thiazole (2BNIT) is a molecule that is commonly used in pharmaceutical preparations. 2BNIT has been shown to be toxic to mammalian cells, and hydrogen chloride (HCl) is produced as a result of the reaction. The HCl acts as an oxidizing agent that can react with nitrothiazole and nitro compounds, releasing ammonia gas. 2BNIT has been shown to have potent activity against three different species of bacteria, including Trichomonas vaginalis, Salmonella typhimurium, and Micrococcus luteus. The compound also has optical properties that can be observed by vibrational spectroscopy.</p>

<p>1,8-Dinitroanthraquinone is an aromatic hydrocarbon that inhibits the growth of bacteria in vitro. This compound has been shown to inhibit telomerase activity and to be a potent inhibitor of monosodium glutamate-induced nitrosative stress in cultured cells. It also inhibits nitrite ion reduction by 2-phenylbutyric acid, which is an acceptor for the nitrite ion. 1,8-Dinitroanthraquinone has been shown to have a kinetic effect on the conversion of nitrite ion to nitrous acid, which is important in the formation of carcinogenic nitrosamines. The paradigm shift in this research was that the inhibition of telomerase activity was not only due to its effects on DNA but also due to its activation energy as well as its effects on protein synthesis.</p>

<p>2-Methoxy-3-nitropyridine is a chemical compound with the molecular formula CHNO. It is classified as an amine and has a molecular weight of 140.24 g/mol. 2-Methoxy-3-nitropyridine is a colorless liquid that can be used to make other compounds, such as nitroarenes, boronic acids, and dyes. The molecule consists of a central carbon atom with four nitrogen atoms at the corners of a tetrahedron. The electron configuration for this molecule is 1s22s22p4. This means that the outer shell electrons are in orbitals with principal quantum numbers s=1 and p=2. These orbitals are located near the middle of the molecule rather than on the periphery as in ethane (CH3CH2). This orientation provides more space for other atoms to attach to the central carbon atom, which increases its affinity for nucleophilic attack. 2-M</p>

<p>2-Amino-3-chloro-5-nitrobenzonitrile is a hydroxyalkyl compound. It is sensitive to light, sulfamic acid and heat. The compound has been expressed in E. coli, but it is not possible to crystallize it due to its sensitivity to ph changes and organic solvents. The substance can be used as a dyestuff or dye intermediate. Due to its stability in crystal form, this substance can also be used as a raw material for the production of nitrite.</p>

<p>2,3-Dichloro-6-nitrobenzonitrile is an organic chemical compound that has a nitrile group and a nitro group. It can be synthesized by the cycloalkylation of ethyl bromoacetate with hydroxylamine. The resulting 2,3-dichloro-6-nitrobenzonitrile is extracted from the reaction mixture with water, acidified with dilute hydrochloric acid, and then precipitated as its ethyl ester salt. The 3D structure of this chemical was determined by X-ray crystallography.</p>

<p>WST-1 is a water soluble cell permeable dye.  Upon NADH-dependent enzymatic cleavage by cellular mitochondrial dehydrogenases, formazan is released, which can be quantified by colorimetric detection at 450 nm.</p>

<p>3-Methyl-2-nitrophenol is a hydroxy group that contains a reactive methylene group. It has been shown to be formed by the reaction of nitric acid with alcohols or amines. The rate of formation is influenced by the steric interactions and intramolecular hydrogen bonds present in the reactants. 3-Methyl-2-nitrophenol can react with other molecules to form various reaction products, such as 2-methylphenol, nitrobenzene, and picric acid. 3-Methyl-2-nitrophenol also has phytotoxic properties, which may be due to its ability to inhibit root growth and chlorophyll production in plants.</p>

<p>3,5-Dimethyl-4-nitropyridine 1-oxide is a nitro compound with the chemical formula CHNO. It is an organic compound that has been shown to be carcinogenic in animal studies and has caused cancer in humans. 3,5-Dimethyl-4-nitropyridine 1-oxide can be found in the environment as a result of industrial accidents or environmental pollution. It is found in building materials such as acetonitrile and organic solvents. This compound is not soluble in water, which limits its potential for environmental transport.</p>

<p>4-Acetamido-2'-amino-2-nitrophenyl sulphide is a versatile building block that is used as a reagent, speciality chemical, and useful scaffold. It is a complex compound with CAS No. 1017060-37-5. This compound has been shown to be useful in the synthesis of fine chemicals and other research chemicals. 4-Acetamido-2'-amino-2-nitrophenyl sulphide can also be used as an intermediate in reactions or as a reaction component, making it an important building block for high quality compounds.</p>

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<p>3,5-Dinitro-1,2-phenylenediamine is an aromatic compound that is used as an anti-cancer drug. 3,5-Dinitro-1,2-phenylenediamine can be synthesized by the reaction of diethyl ester with nitrous acid. This product has been shown to inhibit the growth of cancer cells in culture and is cytotoxic to ovarian cancer cells. 3,5-Dinitro-1,2-phenylenediamine has also been shown to have a synergistic effect with other drugs. It inhibits the synthesis of DNA and RNA by binding to nucleic acids and blocking protein synthesis. This product is not active against bacteria or fungi but may be toxic if ingested.</p>

<p>Methyl 3-fluoro-4-nitrobenzoate is a volatile, colorless liquid that belongs to the class of alcohols. Methyl 3-fluoro-4-nitrobenzoate has a phenylethyl group and an intramolecular reaction with the carbonyl group. The regioselectivity of this reaction is determined by the electron density on the oxygen atom, which is greater than on the nitrogen atom. This makes methyl 3-fluoro-4-nitrobenzoate an excellent nucleophile and allows it to react with other molecules in order to form esters. Methyl 3-fluoro-4-nitrobenzoate has been shown to be a good solvent for headspace analysis because it is volatile, but not reactive enough to interfere with organic compounds in the headspace.</p>

<p>2-Chloro-3-nitrotoluene (2CNT) is a primary site test compound that is used to determine the activity of enzymes that metabolize nitrate. It has been shown to inhibit inorganic nitrate reductase and plant nitrate reductase, which are important enzymes for the transport of nitrogen. The rate of 2CNT degradation increases with increasing temperature, and it is resistant to heat and oxygen. 2CNT also inhibits tobacco N-acetyltransferase, an enzyme involved in the metabolism of nicotine. 2CNT can be used as an inhibitor to study plant physiology because it evaporation occurs rapidly at room temperature.</p>

<p>2-Nitro-3,4,5-trimethoxybenzoic acid methyl ester is a potential anticancer agent. It has been shown to inhibit the growth of cancer cells in vitro and demonstrates anticancer activity against human tumor xenografts in mice. This compound binds to the epidermal growth factor receptor (EGFR) and inhibits its activity. This binding causes downstream signalling pathways to be suppressed, which ultimately prevents tumor cells from proliferating. 2-Nitro-3,4,5-trimethoxybenzoic acid methyl ester also has directional properties that may allow for selective targeting of cancerous cells.<br>2-Nitro-3,4,5-trimethoxybenzoic acid methyl ester is a white crystalline powder with an orthorhombic crystal system and an amine group on each end of the molecule.</p>

<p>L-Leucine 4-nitroanilide serves as a substrate for the colorimetric determination of leucine aminopeptidase. The application of L-Leucine-p-nitroanilide includes its utilization as a substrate in studies assessing the intestinal leucine aminopeptidase activity of juvenile rainbow trout (Oncorhynchus mykiss). Additionally, it plays a role in insulin-regulated aminopeptidase inhibition assays and is employed to determine exopeptidase activity.</p>

<p>Cis-4-Chloro-3-nitrocinnamic acid is an aromatic organic compound with potential utility in biochemical research and synthesis. This compound is typically derived from synthetic chemical processes involving chlorination and nitration reactions on cinnamic acid derivatives. Its molecular structure, characterized by both chloro and nitro functional groups, allows it to interact in unique ways with various biochemical pathways and molecular frameworks.</p>

<p>3,5-Dinitrobenzenethiol is a chemical that has been used as a building block for the synthesis of other fine chemicals. 3,5-Dinitrobenzenethiol is an intermediate used in the synthesis of research chemicals, such as pharmaceuticals and pesticides. It can also be used as a reaction component or reagent in organic synthesis. 3,5-Dinitrobenzenethiol is an excellent chemical with high quality because it has no impurities and is readily available.</p>

<p>Please enquire for more information about Fmoc-(S)-3-amino-3-(2-nitrophenyl)propionic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-tert-Butyl-2,6-dinitroanisole is a versatile chemical that can be used for the synthesis of complex molecules. It can be used as a building block in organic synthesis or as a reagent. 4-tert-Butyl-2,6-dinitroanisole is also useful in the production of speciality chemicals and research chemicals. This product has high quality and is a useful intermediate or reaction component.</p>

<p>2-Benzyloxy-6-nitrotoluene is an organic compound that has the formula CHNO. It is a white solid that is soluble in alcohols and ethers, but not in water. The compound is of interest as a precursor to other compounds.</p>

<p>3-Amino-4-nitrobenzoic acid is a synthetic compound, which has been shown to inhibit the activity of trypanothione reductase. This inhibition of the enzyme causes an increase in the level of intracellular trypanothione, which is then acetylated by ATP sulfurylase and converted to trypanothione. 3-Amino-4-nitrobenzoic acid is also a potent inhibitor of fxa, which is a coagulation factor necessary for blood clotting. The active site of 3-amino-4-nitrobenzoic acid contains two nitroarenes that are responsible for its antithrombotic properties.</p>

<p>Substrate to study the nitroreductase activity in the pathogenic fungus Sporothrix schenckii, a thermal dimorphic pathogenic fungus causing a subcutaneous mycosis.</p>

<p>4-Chloro-3,5-dinitrobenzamide is a bifunctional molecule that contains a chlorine atom. It has been found to react with dipolar solutes as well as vicinal dioxan arylation. The nucleophilic amide group is also labile and can be hydrolyzed by strong acids or bases. The electron lone pair of the chlorine atom in 4-chloro-3,5-dinitrobenzamide can be used for electrophilic substitution reactions with aromatic rings or amines. This molecule has been found to undergo an arylation reaction with imidazole in the presence of dioxan solvent at room temperature.</p>

<p>2-Nitrobenzylcyanide is a potential use in the synthesis of β-unsaturated ketones, nitroalkanes, and biomolecular compounds. This compound reacts with nitrogen atoms to form an unsymmetrical nitrene group. The reaction selectivity is due to the active methylene group that is acidic, which selectively reacts with amines or cb1 receptor groups.</p>

<p>4-(2-Hydroxyethylamino)-3-nitrophenol is a nitrophenol that can cause toxicity in humans. It has been investigated for its potential use as a treatment for erectile dysfunction. The compound was found to have a long half-life of over 24 hours, which may be due to its slow metabolism by esterases and glucuronidases. 4-(2-Hydroxyethylamino)-3-nitrophenol has been shown to be an allergen and is toxic to the skin, lungs, and muscles. This chemical can cause cancer when it is irradiated or mixed with other chemicals such as 4-amino-2-nitrophenol (ANP).</p>

<p>2-Nitro-3,4,5-trimethoxybenzoic acid (2-NTMB) is a potent anticancer agent that has shown cytotoxic effects in human epidermoid carcinoma cells. It inhibits the growth of cancer cells by interfering with their DNA synthesis and repair. 2-NTMB binds to DNA and blocks the action of enzymes involved in DNA synthesis and repair. This binding leads to cancer cell death through irradiation or by blocking the production of new proteins vital for cell division. 2-NTMB is bioisosteric with combretastatin A4, which means it can be substituted for this drug without significant loss of potency. It also has been shown to be an effective chemotherapeutic agent against breast cancer in mice.</p>

<p>2-Bromo-5-nitroaniline is an aminobenzothiazole that is synthesized in an amination reaction with acetonitrile. It is an acidic chemical and can be introduced as a pharmacokinetic probe for studying the uptake of drugs by cells. The properties of 2-bromo-5-nitroaniline have been studied in mice and rats, where it has been shown to be metabolized by nitroreductases. 2-Bromo-5-nitroaniline can also be used as a chemokine receptor antagonist, which could lead to the optimization of other chemokines.</p>

<p>3-Methyl-2-nitroanisole is a synthetic monosubstituted nitro compound that can be produced by the oxidation of 3,4-dimethoxybenzaldehyde. It has three methyl groups and one nitro group on its ring. 3-Methyl-2-nitroanisole has been used in high concentrations as a reactant for the synthesis of other compounds. It can also be used to synthesize anthranilic acid, which is an intermediate in the synthesis of many dyes and pharmaceuticals. 3-Methyl-2-nitroanisole has been characterized using vibrational spectroscopy and NMR spectroscopy with frequency values ranging from 9 to 22 cm/sec, depending on substituents. The molecular weight is estimated at 196 g/mol. 3MNA has been shown to undergo demethylation and hydrolysis under acidic conditions to produce 2,5-dihydroxyanth</p>

<p>3,4-Dihydroxy-5-nitrobenzaldehyde is a chemical substance that is used in an analytical method to measure the level of methoxy groups in chronic kidney disease. The methanol solvent and hydrochloric acid are used to dissolve the sample, which is then titrated with trifluoroacetic acid. The chloride ion reacts with the methylene group from the 3,4-dihydroxy-5-nitrobenzaldehyde molecule to form a new compound that can be detected by ultraviolet light at 254 nm. The active methylene group is quantified by measuring its absorbance at this wavelength and comparing it with a calibration curve using known concentrations of sodium salts. This test has been shown to be more sensitive than other chromatographic methods for detecting methoxy groups in chronic kidney disease.</p>

<p>O-(2,4-dinitrophenyl)hydroxylamine is a synthetic compound that binds to the enzyme bound site of the cap-dependent endonuclease. It is an inhibitor of influenza virus replication in vitro and has shown inhibitory activity against murine leukemia virus. O-(2,4-dinitrophenyl)hydroxylamine is also a model for the study of aminoglycoside antibiotics. The compound inhibits aminoglycoside-induced protein synthesis in eukaryotic cells and may be useful in understanding the mechanism of action and resistance to these antibiotics.</p>

<p>2,6-Dichloro-4-nitroaniline is an organic compound that has been shown to have anti-inflammatory properties. It can be used for the treatment of inflammatory skin diseases such as psoriasis and eczema. Short-term exposure to 2,6-dichloro-4-nitroaniline showed no toxic effects in cell culture studies and 2,6-dichloro-4-nitroaniline does not cause damage to skin cells or light exposure. The hydroxyl group on the aromatic ring of this molecule can react with hydrochloric acid to form a reactive intermediate. This intermediate reacts with N2H2 molecules to form a molecule called dinitrochlorobenzene. Dinitrochlorobenzene is a highly toxic substance that will react with nitrogen atoms on the cell wall surface in an acidic environment, forming nitrosamines which are highly carcinogenic compounds.</p>

<p>2-Chloro-3,5-dinitrobenzoic acid is a chemical reagent that belongs to the group of p2-substituted benzenes. It is used in organic synthesis as a synthon for dimethylnaphthalene, which is an intermediate in the production of polyester fibers and polyurethane. The compound has been shown to induce apoptosis in prostate cancer cells. This effect may be due to its ability to react with amines and form nitrosating species, which may cause DNA damage. 2-Chloro-3,5-dinitrobenzoic acid can also react with 5-nitrosalicylic acid to form a stepwise reaction product.</p>

<p>3,4-Dihydroxy-2-nitrobenzyl alcohol is a fine chemical that is useful as a scaffold and building block for organic synthesis. It is also an intermediate in the preparation of other chemicals such as reaction components. 3,4-Dihydroxy-2-nitrobenzyl alcohol has CAS No. 1017060-58-0 and belongs to the speciality chemical category. This compound can be used as a reagent or research chemical in biochemical assays and other applications. 3,4-Dihydroxy-2-nitrobenzyl alcohol is soluble in methanol, ethanol, acetone, dichloromethane, ethyl acetate, and chloroform. It is insoluble in water and ether. It is stable at pH values between 2 and 10 but decomposes when heated to 80°C or above.</p>

<p>4-Nitrocinnamaldehyde is a diazonium salt that is used as an efficient method for the synthesis of nitro compounds. Nitro compounds are used in the production of explosives, insecticides, and herbicides. 4-Nitrocinnamaldehyde reacts with hydrochloric acid to produce trifluoroacetic acid, which is then reacted with an organic compound to produce a nitro compound. This reaction has been shown to be irreversible and not sensitive to functional groups. 4-Nitrocinnamaldehyde binds to the enzyme cytochrome P450 reductase, inhibiting its function. The binding of 4-nitrocinnamaldehyde to enzymes such as pyruvate kinase and acetylcholinesterase has also been observed in binding experiments.</p>

<p>3-Nitrophenol is an organic compound that is used in wastewater treatment, specifically to remove nitrogenous compounds from the water. It reacts with a hydroxyl group and a nitro group to form a molecule with three nitro groups. The presence of this molecule in wastewater can lead to population growth, which may be reduced by thermal expansion. 3-Nitrophenol is also used as an electrode for gravimetric analysis of metals and as a reagent for the detection of sodium ions. This compound has been shown to have a ph optimum of 7.5, but will react with hydrogen bonds at any ph value.</p>

<p>2,4-Dichloro-beta-methyl-beta-nitrostyrene is a versatile building block that can be used as a reaction component or reagent for the synthesis of other fine chemicals. It is also a useful intermediate for the production of complex compounds. 2,4-Dichloro-beta-methyl-beta-nitrostyrene has been widely used in research and development due to its high quality and versatility. This compound is also available from Sigma Aldrich at competitive prices.</p>

<p>4-Chloro-3-nitrobenzyl alcohol is a synthetic chemical that reacts with hydrochloric acid to form 4-chloro-3-nitrobenzyl chloride and hydrogen. It can be used in the preparation of other chemicals, such as divinylbenzene and chloride. This compound is insoluble in water and soluble in organic solvents, such as acetone and ether. 4-Chloro-3-nitrobenzyl alcohol has two stereoisomers, one of which is more reactive than the other.</p>

<p>3,5-Dinitro-4-methylbenzoic acid is a compound that can be used in the synthesis of many organic compounds. It is an important reagent for the preparation of nitroarenes and it is also used as a precursor to other organic compounds. 3,5-Dinitro-4-methylbenzoic acid has been shown to have a hydrogen bond with malonic acid and can form an asymmetric hydrogen bond with the hydroxyl group of protonated water. 3,5-Dinitro-4-methylbenzoic acid has three different resonance structures and its x-ray diffraction data show that it has a cavity shape. This molecule can be found in the nmr spectra at around 8.3 ppm and its kinetic constants are given as k1 = 0.01 s−1 and k2 = 0.06 s−1 for the two reactions. 3,5-Dinitro-4-methylben</p>

<p>2,4-Dinitro-5-methylphenylhydrazine (DMN) is a fine chemical that is used as a versatile building block in the synthesis of complex compounds. It can be used to synthesize high quality reagents and reaction components for research purposes. DMN has been shown to have a number of properties that make it useful in industrial processes, including its stability and resistance to heat and light.</p>

<p>N-Nitrosobis(2-hydroxypropyl)amine is a polymerase chain reaction (PCR) enhancer that has been shown to be carcinogenic in experimental animals. It is used as a synthetic retinoid, which results in the conversion of thyroxine to triiodothyronine by the thyroid gland. N-Nitrosobis(2-hydroxypropyl)amine is also used as an experimental model for squamous cell carcinoma and tumors. It causes tumor development by inhibiting DNA synthesis and increasing cellular proliferation, which leads to liver lesions and carcinomas in animal models.</p>

<p>4-Bromo-3-nitrotoluene is a carbazole that has been found to have insecticidal activity. The compound reacts with serotonin to form the reactive intermediate 4-bromo-3-nitrosobenzaldehyde, which is then oxidized to the final product 4-bromo-3-nitrobenzoic acid. The insecticidal activity of 4-Bromo-3-nitrotoluene was found to be due in part to its ability to inhibit serotonin uptake and metabolism by blocking serotonin transporters. It also induces dihedral angles in positron emission tomography (PET) imaging of human brain tissue, suggesting it may be useful for brain imaging studies.</p>

<p>Please enquire for more information about Methyl 4-(2-nitro-4-(trifluoromethyl)phenoxy)benzoate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Chloro-4-nitrobenzaldehyde is an aldehyde that is produced by the oxidation of 2-chloro-4-nitrobenzaldehyde. This chemical has been shown to have antitubercular activity in human erythrocytes, and it can be recycled from its reaction product with sodium hypochlorite. 3-Chloro-4-nitrobenzaldehyde has been shown to interact with acidic heterocycles such as oxadiazoles and triazoles. 3-Chloro-4-nitrobenzaldehyde has also been shown to alter the morphology of bacteria, such as subtilis, when exposed to ionic liquids. It is also known to inhibit the growth of Gram positive bacteria and show cytotoxic effects on mammalian cells.</p>

<p>5-Methyl-2-nitrobenzamide is a compound that has antiproliferative activity and is used as an anticancer drug. This drug inhibits the polymerization of the protein tubulin in cancer cells, thereby inhibiting cell division. It also inhibits the growth of certain tumor cell lines in vitro. 5-Methyl-2-nitrobenzamide was found to inhibit the proliferation of human ovarian carcinoma cells by binding to DNA, preventing transcription and replication of genetic information. In addition, this agent binds to tubulin and prevents its polymerization, leading to inhibition of cell division.</p>

<p>Tribromonitromethane is a fatty acid that is used in analytical chemistry as a standard for calibrating the linear range of analytical methods. It is also used in specific treatments for cancer, such as treatment of carcinomas. Tribromonitromethane has been shown to have carcinogenic potential and may be harmful to humans when ingested or inhaled. The chemical structure of tribromonitromethane consists of a series of three bromine atoms attached to one carbon atom with two hydroxyl groups at either end. This chemical can be oxidized to form tribromo nitro methane, which is more reactive than tribromonitromethane. Tribromonitromethane has no known biological function and does not occur naturally in the environment. It is also known to be potent inducers of transfer reactions, which are reactions where electrons are transferred from one molecule to another. These reactions are important for the synthesis and degradation of various molecules, including amino</p>

<p>3,4-(Methylenedioxy)-6-nitrocinnamic acid is a cytotoxic molecule that inhibits the growth of cells by interfering with the synthesis of proteins. It binds to DNA and prevents the transcription process from occurring. This molecule has been shown to inhibit endoplasmic reticulum and Golgi apparatus functions in plant cells. 3,4-(Methylenedioxy)-6-nitrocinnamic acid has also been used as a polymerization agent for polyacrylamide gels. A number of modifications have been made to this molecule in order to increase its effectiveness, such as methyl esterification and mutagenesis. This compound has also been shown to enhance Taxol's anti-cancer effects on cell cultures.</p>

<p>4-Methyl-3-nitrobenzenesulfonyl chloride (4MNBS) is a fungicide that inhibits the growth of fungi, such as Plasmodiophora brassicae, by inhibiting the enzyme dehydrogenase. 4MNBS has also been shown to inhibit mammalian pyridine nucleotide dehydrogenase and to have low toxicity in mammals. 4MNBS has been found to be an inhibitor of human cytochrome P450 isoforms CYP1A2, CYP2B6, and CYP3A4 with IC50 values ranging from 10 μM to 100 μM. 4MNBS was also shown to be a potent inhibitor of chloroplast dehydrogenases from cruciferous plants with IC50 values between 0.1 μM and 100 nM. This compound has low phytotoxicity and does not accumulate in the leaves of cruciferous plants at a concentration of 500 ppm or higher.</p>

<p>4-Chloro-2-fluoro-5-nitroaniline is a fine chemical that is used as a reagent and speciality chemical in research, as well as a building block for the synthesis of complex compounds. 4-Chloro-2-fluoro-5-nitroaniline has been shown to be an excellent building block for the synthesis of versatile scaffolds, which can be used in the production of drugs with antibacterial properties. This product is also useful as a reaction component for the synthesis of high quality, complex compounds.</p>

<p>Methyl 5-hydroxy-2-nitrobenzoate is a synthetic pesticide that is used to control pests in animals. It has been shown to be an antigen that induces antibody production in mice. This chemical is also a ligand, as it binds with proteins and other molecules. Methyl 5-hydroxy-2-nitrobenzoate has been shown to inhibit the enzymatic activity of the organophosphorus pesticide, which is primarily used for pest control. The chemical was also found to inhibit the growth of plants by inhibiting protein synthesis and cell division at low concentrations.</p>

<p>Ethyl 3-nitrobenzoate is an organic compound that belongs to the methyl ketones group. It is a colorless liquid with a sweet, aromatic odor. Ethyl 3-nitrobenzoate has been shown to interact with benzocaine and other local anesthetics, which may lead to its use as a precursor for these drugs. It can also be used as a carbon source for bacterial cells and can be used in an efficient method for the synthesis of antigenic determinants. This compound has been shown to have anticomplementary properties and may be useful in treatment of bacterial infections.</p>

<p>Methyl 3-methyl-4-nitrobenzoate is a potential antitumor agent that has been shown to have minimal inhibitory concentrations against a variety of human tumor cell lines. It also has potent antifungal activity and can be used for the treatment of opportunistic fungal infections in humans. Methyl 3-methyl-4-nitrobenzoate may be modified by substituting or deleting the aromatic ring, which can lead to improved inhibitory properties. Methyl 3-methyl-4-nitrobenzoate can also be modified by replacing the methyl group on the nitro group with a fluorine atom, which changes its structure and enhances its inhibitory potency.</p>

<p>4-Methyl-5-nitrocatechol is a nitro compound that has been used in the chemical ionization of samples for mass spectrometric analysis. This compound produces distinct x-ray absorption spectra and emission spectra, which can be used to identify its concentration. 4-Methyl-5-nitrocatechol has been shown to react with 3,5-dinitrosalicylic acid in the presence of light to form an inhibitory product that prevents the growth of bacteria. This reaction is more prevalent at elevated temperatures. The mutant strain of Escherichia coli was found to be resistant to this inhibitory effect, while the wild type strain was not. The mutant strain's resistance to this inhibitory compound may be due to a polymerase chain reaction mutation that increases its ability to replicate DNA at high temperatures.</p>

<p>2-Fluoro-5-nitrobenzonitrile is a reactive chemical that has been used to study the interaction of amines with nitro groups. It can react with serine protease and acetylcholine, forming a lactam intermediate. The reaction of 2-fluoro-5-nitrobenzonitrile with hydrogen peroxide produces oxygen gas, water, and nitrous acid. The reaction of 2-fluoro-5-nitrobenzonitrile with benzamidine produces phenylhydrazine and benzoic acid. This chemical has shown anti-cancer activity in cell culture studies, as well as inhibition of cancer cell growth in vivo. 2-Fluoro-5-nitrobenzonitrile is also an inhibitor of the enzyme nitric oxide synthase (NOS). It reacts with the heme group in NOS, which prevents the formation of NO from L-arginine.</p>

<p>Please enquire for more information about 4,6-Diamino-2-nitro-m-xylene including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Applications (αS)-α-Amino-4-nitrobenzenepropanamide (cas# 81677-61-4) is a compound useful in organic synthesis.<br></p>

<p>Applications 2-Phenyl-4-nitrosophenol is an intermediate in the synthesis of (E)-2-((6-Hydroxy-[1,1'-biphenyl]-3-yl)((6-hydroxy-[1,1'-biphenyl]-3-yl)imino)methyl)benzoic Acid which is an impurity of (S)-Cloperastine (C587195); a drug used in the treatment of chronic non-productive cough. Also antitussive.<br>References Aliprandi, P. et al.: Drugs Exp. Clin. Res., 30, 133 (2004); Aliprandi, P. et al.: Clin. Drug Invest. 22, 209 (2002)<br></p>

<p>Applications Methyl 5-nitroisophthalate is used in the preparation of heterotrifunctional crosslinkers for multiple bioconjugation with peptides and also in the synthesis of histone demethylase LSD1 inhibitors that target cancer cells.<br>References Wang, J. et al.: Cancer Res., 71, 7238 (2011); Viault, G. et al.: Org. Biomol. Chem., 11, 2693 (2013);<br></p>

<p>Applications Phosphorylating reagent<br></p>

<p>Applications 6,7-Dinitro-2,3-dihydro-benzo[1,4]dioxime (cas# 57356-48-6) is a compound useful in organic synthesis.<br></p>

<p>Applications 2-Nitrobenzylcyanide (cas# 610-66-2) is a compound useful in organic synthesis.<br></p>

<p>Applications 3-Nitro-4-toluidine (cas# 119-32-4) is a compound useful in organic synthesis. Dyes and metabolites, Environmental Testing<br></p>

<p>Applications 2,4-Dinitrobenzenesulfonic Acid (cas# 89-02-1) is a useful research chemical.<br></p>

<p>Applications 2-(4-Nitro-2-ethoxyphenyl)pthalimide (cas# 106981-60-6) is a compound useful in organic synthesis.<br></p>

<p>Applications 4-Benzyloxy-2-(2’-carbomethoxy)thiophenylnitrobenzene (cas# 329217-03-0) is a compound useful in organic synthesis.<br></p>

<p>Applications (cas# 1999-08-01) is a useful research chemical.<br></p>

<p>Applications 1-Methyl-2-nitrobenzene is a toxic pollutant of the environment because of its large scale use in the production of explosives. It is a useful synthetic intermediate. It shows carcinogenic activity in rats.<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 Sikandar, M., et al.: Chemosphere, 90, 1920 (2013); Jones, C., et al.: Carcinogen., 24, 779 (2003)<br></p>

<p>Applications Derivative of Salicylic acid.<br></p>

<p>Applications 4-Nitrobenzonitrile (cas# 619-72-7) is a useful research chemical.<br></p>

<p>Applications Methyl 4-nitrobenzoate (cas# 619-50-1) is a useful research chemical.<br></p>