Nitro

<p>4-Bromo-3,5-dinitroaniline is a versatile chemical intermediate that has been used in the synthesis of various drugs. This compound is a fine chemical that is not available at any commercial level and can be obtained from research chemicals suppliers. It has been found to be useful as a building block in the synthesis of chemicals such as pharmaceuticals and agrochemicals. The CAS number for this compound is 62554-90-9.</p>

<p>4-Nitro-3-iodoanisole is a bauerine that is used as a ligand in asymmetric catalysis. It is an atropisomeric compound, meaning it can exist in two different forms. The two forms of 4-nitro-3-iodoanisole are identical except for the orientation of the axial ligands on opposite sides of the molecule. The axial ligands on one form are biphenyl and nitrous oxide, while the axial ligands on the other form are nitrous oxide and biphenyl. 4-Nitro-3-iodoanisole has been used to catalyze reactions such as alkylation and coupling reactions with a variety of substrates, including β-carbolines, phenols, and amines.</p>

<p>CAS No. 137391-68-5 is a fine chemical that is used as a building block in organic chemistry research and as a reagent, speciality chemical, or intermediate. This compound has been shown to be useful in the synthesis of complex compounds and can be employed as a versatile building block for the synthesis of pharmaceuticals and other chemicals. This compound has also been shown to be an excellent reaction component, making it an ideal scaffold for the construction of larger molecules.</p>

<p>2-Methyl-3-nitroaniline is a nitro compound that is used in the synthesis of diazonium salts. It is a white solid with an unpleasant odor. 2-Methyl-3-nitroaniline can be obtained by reacting picric acid with hydroxide solution and nitrous acid, or by the reaction of ammonia with amines. This compound has been shown to possess magnetic resonance spectroscopy properties and has been used for the detection of cellulose content in wheat samples.</p>

<p>3-Methoxy-5-nitrobenzoic acid is an organic compound that has mesomorphic and switchable properties. It is a chalcone derivative, with homologues such as 3-hydroxybenzoic acid. It is synthesized from the reaction of nitrous acid and 3-methoxybenzoic acid. The synthesis of this compound can be achieved by two different routes: peroxide oxidation or fluorine substitution. Both routes produce the same product, but offer different advantages. The first route involves the addition of hydrogen peroxide to 3-methoxybenzoic acid, which produces a mixture of products containing 3-methoxy-5-nitrobenzoic acid. This route is advantageous in that it can be conducted at room temperature with high yields, but the disadvantage is that this method produces a mixture of products which may contain undesired byproducts. The second route involves the use of sodium hypofluorite and potassium</p>

<p>2-Amino-N-[2-(2-chlorobenzoyl)-4-nitrophenyl]acetamide is a fine chemical that is used as a building block in organic synthesis. It is a versatile intermediate for the synthesis of other compounds and can be used to make a variety of useful scaffolds. 2-Amino-N-[2-(2-chlorobenzoyl)-4-nitrophenyl]acetamide has been used in research and development of pharmaceuticals, agrochemicals, herbicides, and other compounds.</p>

<p>3-Nitro-4-methoxybenzamide is a versatile building block that belongs to the group of fine chemicals. It is a reagent that is used in the synthesis of complex compounds. 3-Nitro-4-methoxybenzamide has been shown to be an effective intermediate for the synthesis of pharmaceuticals, such as antibiotics and immunosuppressants. This compound also has high quality and can be used as a scaffold for other chemical syntheses.</p>

<p>2-Fluoro-4-nitroaniline is a molecule that has been shown to have clinical studies in industrialized countries. It is a hydrophobic molecule, which means it does not dissolve in water. 2-Fluoro-4-nitroaniline binds to the 5HT receptor subtype with an energy of -1.89 eV and inhibits cancer cell proliferation by inhibiting the activation of 5HT receptors. The reaction mechanism for this drug involves the transfer of an electron from the hydrogen atom to the nitro group on the compound, which creates a radical cation (R+). This radical cation interacts with oxygen and forms a peroxyl radical, which reacts with nearby molecules and causes damage to them. The molecule is then broken down by enzymes called peroxidases.</p>

<p>N-Nitrosopiperidine is a nitrated aromatic amine that can be found in the environment. It has been shown to induce genotoxic effects and to inhibit liver microsomal enzyme activity. It is also shown to cause DNA damage in hl-60 cells and in the model system. N-Nitrosopiperidine may act by causing an increase in reactive oxygen species (ROS) production, which results in oxidative stress and cellular dysfunction. This compound has been shown to induce congestive heart failure, as well as chronic oral toxicity and maternal toxicity. N-Nitrosopiperidine has also been associated with hepatic tissues changes and fetal bovine abnormalities.</p>

<p>3,4-Dimethyl-6-nitrobenzoic acid is a nitrated aromatic compound that has been shown to have anticancer activity. It is used as an anticancer agent in the treatment of cancers such as leukemia, lymphoma, and lung cancer. 3,4-Dimethyl-6-nitrobenzoic acid has been shown to be effective against species diversity and diversity of tumor cells. This compound inhibits protein synthesis by binding to ribosomes and inhibiting the production of proteins vital for cell division. 3,4-Dimethyl-6-nitrobenzoic acid also binds to DNA and interferes with transcription and replication of DNA, causing cell death. This compound has been found in wetlands (e.g., <br>the Yangtze River) but its function in these ecosystems is not known.</p>

<p>2,3,4,5-Tetrahydro-7,8-dinitro-3-(trifluoroacetyl)-1,5-methano-1H-3-benzazepine is a supplement that may be used to treat depression. It has been shown to have a receptor activity on the acetylcholine receptors. 2,3,4,5-Tetrahydro-7,8-dinitro-3-(trifluoroacetyl)-1,5-methano-1H-3-benzazepine has also been shown to increase the activity of the endothelial function by increasing the production of nitric oxide. This drug has also been shown to be an effective treatment for reducing appetite in cases of anorexia nervosa and for treating Alzheimer's disease. The drug works by activating nicotinic acetylcholine receptors in the brain.</p>

<p>3-Fluoro-4-nitroanisole is a regiospecific synthesised compound that binds to albumin in the human serum. It has been shown to be an endogenous metabolite of 3-fluoro-4-nitrophenol, which is a potent inhibitor of cellular and blood assays for amines. The binding affinity for albumin was about 100 times higher than for other amines such as histamine or tyramine. 3-Fluoro-4-nitroanisole also has a high affinity for anions, with a pKb value of 8.7, which makes it suitable as an anion receptor in applications such as the determination of anion concentration in water samples. This fluoroquinonoid is also used as a fluorescent probe for nucleophilic reactions and can be used to detect nucleophiles in organic solvents by adding it to the reaction mixture.</p>

<p>2-Bromo-5-chloronitrobenzene is a synthetic drug that has been shown to inhibit the growth of cancer cells. It is a potent antagonist at the tyrosine kinase receptor, which may be involved in the development of some cancers. The drug was first synthesized in 1887 by German chemists for use as an antipsychotic drug, but it was not until 1962 that researchers discovered its therapeutic value in treating schizophrenia. Clozapine also blocks the activity of other receptors including factor receptors and growth factors, which may account for its antitumor effects. Clozapine has also been used to treat resistant breast cancer cases with imatinib therapy.</p>

<p>4-Chloro-3-nitrobenzoic acid methyl ester is a chemical compound that inhibits the synthesis of nucleic acids. It binds to the functional groups of DNA, preventing replication and transcription. 4-Chloro-3-nitrobenzoic acid methyl ester also inhibits protein synthesis by inhibiting ribosomal RNA which is required for translation. This agent has been shown to induce apoptotic cell death in leukemia cells, HL60 cells, and other types of cancer cells in vitro. 4-Chloro-3-nitrobenzoic acid methyl ester has a potent inhibitory activity against replicons in vitro and is a synthetic molecule with two sulfoxide functional groups.</p>

<p>5-Nitro-pyridine-2-sulfonyl chloride is a chemical reagent that is used in the synthesis of various organic compounds. It is a versatile building block and can be used as an intermediate for the synthesis of other compounds. 5-Nitro-pyridine-2-sulfonyl chloride is also a reaction component in the synthesis of some pharmaceutical drugs, such as benzoic acid, which can be used to manufacture more complex compounds, such as antibiotics.</p>

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

<p>1-Chloro-2,6-dinitrobenzene is a synthetic compound that has been shown to be an effective antiviral agent in vitro. It has a high affinity for nucleophilic sites and can react with the nitro group of compounds to form dinitrobenzoic acid derivatives. 1-Chloro-2,6-dinitrobenzene is highly reactive and can undergo thermolytic decomposition, which limits its use as an antiviral agent. This chemical is not active against HIV or influenza A virus strains.</p>

<p>Ethyl 3,5-dinitrobenzoate is an ethyl ester of 3,5-dinitrobenzoic acid. It is used as a stabilizer for polymers and plastics. It has been shown to be effective in the analysis of molecular descriptors, with a high molecular weight and moderate polarity. This molecule has not been found to have any amine groups or nitro groups, but does contain one hydroxyl group and two methyl groups. Ethyl 3,5-dinitrobenzoate also contains one carboxylic acid group that can form an ester with a second molecule. The refractive index is 1.638 and the inorganic content is 0%. The malic acid content is 12%. Regression analysis shows that the melting point of this compound is 93 degrees Celsius.</p>

<p>Methyl 4-bromo-3-nitrobenzoate is a methoxy-substituted methyl ester of 3-nitrobenzoic acid. It has been shown to bind to copper ions with high affinity, and can be used to regulate the uptake of copper ions in cells. Methyl 4-bromo-3-nitrobenzoate is a ligand for many metal ions, and can be used as a predictable, conformationally constrained framework for drug design. Selectivities are achieved by carboxylate substituents and nitro groups on the benzene ring. The asymmetric center allows for conformational control of the molecule, which can be exploited in drug design.</p>

<p>The reaction of 2,3,5-trimethyl-4-nitropyridine 1-oxide with hydrogen peroxide is an example of a peroxide reaction. The HOOH molecule is a nucleophilic and attacks the CNO group. This leads to the formation of a new bond between the oxygen and carbon atoms in the molecule. The oxygen atom then becomes an oxidizing agent, which can react with other molecules in order to form more products. In this reaction, hydrogen peroxide is used as an oxidizing agent to produce chlorine gas, water vapor, and nitric oxide gas. The reaction can be summarized as follows: 2CNO + 3HOOH → 4CO + 2O + 3N2O + 3HO2</p>

<p>2-(2,4-Dinitrophenoxy)ethanol is a glycol ether that has been shown to be an effective nucleophile in nucleophilic substitution reactions. It is a colorless liquid with a boiling point of between 204°C and 205°C. 2-(2,4-Dinitrophenoxy)ethanol reacts with deionized water in the presence of ethylene to produce a crystalline precipitate. The product can be recrystallized from ethanol/water or purified by chromatography on silica gel. This chemical can also be used as an activated nucleophile in the synthesis of spirocyclic compounds and isomeric ketones. 2-(2,4-Dinitrophenoxy)ethanol is toxic and may cause severe skin burns if it comes into contact with unprotected skin. It is also environmentally hazardous when released into the environment because it breaks down slowly and may accumulate in soil or water systems.</p>

<p>4-Chloro-2-nitrobenzoic acid is a hydrogen bond donor with a coordination geometry of tetrahedral. It has two functional groups: an organic acid and a nitro group. This compound has been used in molecular modeling to study telomeric interactions. 4-Chloro-2-nitrobenzoic acid is also found in biological systems such as the enzyme chloramphenicol acetyltransferase and the antibiotic chloramphenicol. 4-Chloro-2-nitrobenzoic acid can be synthesized from phosphorus pentachloride and amine, which are both commercially available.</p>

<p>4-Nitrocatechol is a reactive chemical that has been used as an analytical reagent for the detection of nitrite ions. It reacts with nitrite ion to form stable complexes, which can be detected by titration calorimetry. 4-Nitrocatechol has also been used as a model for study of reaction mechanisms and coordination geometry. The reaction mechanism of 4-nitrocatechol is thought to involve formation of a dinucleotide phosphate intermediate and subsequent attack by the nitrite ion to produce an unstable intermediate that decomposes to form stable complexes with the nitrite ion.</p>

<p>6-Nitroindoline is a nitro compound that inhibits the polymerization of nitrite. It is an acidic acceptor and has been used as an agrochemical to inhibit nitrification in soil. 6-Nitroindoline has been shown to be mutagenic, which may be due to its ability to form covalent bonds with DNA bases or alkylate DNA bases. 6-Nitroindoline can also undergo borohydride reduction, which is the conversion of a compound into a more reduced form by reaction with borohydride.</p>

<p>1-(3-Chlorophenyl)-2-nitroethene is a reagent that is used as an intermediate in the production of fine chemicals, research chemicals, and speciality chemicals. It has been shown to provide a useful scaffold for the synthesis of complex compounds and is also a versatile building block that can be used in a variety of reactions. 1-(3-Chlorophenyl)-2-nitroethene is not intended for use as a drug or food additive.</p>

<p>Methyl 4-nitrocinnamate is a potential drug candidate for the treatment of cancer. Methyl 4-nitrocinnamate is an analog of cinnamic acid and has been shown to inhibit tumor growth in experimental models. The structural modifications that have been made to methyl 4-nitrocinnamate allow it to be more potent than cinnamic acid. This compound has also shown activity against other types of cancer cells, including breast, colorectal, and prostate cancers. Methyl 4-nitrocinnamate binds to diphenolase enzymes and inhibits their activity, which may lead to its anticancer effects.</p>

<p>5-Chloro-2-nitrobenzonitrile is a nucleophilic compound that inhibits bacterial growth by means of an attack on the sulfhydryl group. 5-Chloro-2-nitrobenzonitrile has shown antibacterial activity against Streptococcus faecalis and Staphylococcus aureus. This drug also has anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis. The molecule has been shown to bind to chloride ions and sulfinyl groups, as well as being able to form a stable complex with erythrocytes in vitro (X-ray crystal structures).<br>5-Chloro-2-nitrobenzonitrile is structurally similar to fluoroquinolones and cephalosporins, which have been shown to have an oral bioavailability of 100%.</p>

<p>2-Hydroxy-5-nitrophenyl)acetone is a high quality reagent that has been used as an intermediate in the synthesis of many complex compounds. It is a useful intermediate and building block in organic synthesis. 2-Hydroxy-5-nitrophenyl)acetone is also a versatile building block, which can be used to form chemical derivatives with different functional groups.</p>

<p>1-(4-(Trifluoromethyl)phenyl)-2-nitroethene is a high quality reagent, which is used as a useful intermediate in the production of fine chemicals. It is also a useful scaffold for the synthesis of speciality chemicals and research chemicals. 1-(4-(Trifluoromethyl)phenyl)-2-nitroethene can be used as a versatile building block for organic synthesis reactions.</p>

<p>3-Hydroxy-2-nitrobenzoic acid is a metabolite of 3-hydroxyanthranilic acid, which is an intermediate in the biosynthesis of amino acids. It can be found in animals and plants. 3-Hydroxy-2-nitrobenzoic acid has two isomers: 3,5-dihydroxybenzoic acid and 3,4,5-trihydroxybenzoic acid. The former is more abundant than the latter. In animal tissues, 3-hydroxybenzoic acid can be found as a diacid or as a salt with sodium or potassium. It reacts with various compounds to form oxidation products that have been shown to have sequences that are different from those of their precursors. These oxidation products are analyzed for the presence of their carboxylate group to identify the original compound. This carboxylate group can then be used as a ligand in matrix assisted laser desorption</p>

<p>4-tert-Butyl-2,6-dinitrophenol is a yellowish solid that is soluble in organic solvents. It is used as an intermediate for the synthesis of dyes, pesticides and pharmaceuticals. 4-tert-Butyl-2,6-dinitrophenol has been shown to cause respiratory tract irritation and narcosis in animals. The toxic effects of 4-tert-Butyl-2,6-dinitrophenol are due to its high electrophilicity and nitro group (NO) which causes oxidative stress. The logistic regression analysis showed that the population growth of ciliates was negatively affected by the presence of halogens in the water.</p>

<p>Please enquire for more information about N-(2-(3,4-dimethoxyphenyl)ethyl)(4-nitrophenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Nitrobenzaldehyde is an organic compound that is used in the synthesis of monoclonal antibodies for use in cancer research. It has been shown to have genotoxic and carcinogenic effects, as it binds to nucleic acids and inhibits DNA replication. 3-Nitrobenzaldehyde has been shown to be effective against a variety of bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and Clostridium perfringens. This compound also inhibits protein synthesis by binding with amines and hydrogen bonding with the amino acid residues of proteins.</p>

<p>2-Nitrofluorene is a reactive compound that is not naturally found in the environment. It is an inhibitor of cytochrome P450 enzymes and can be used in probiotic bacteria as a selective agent for genotoxic compounds. 2-Nitrofluorene inhibits the production of reactive oxygen species and has been shown to induce liver lesions in rats after oral exposure. This compound also induces DNA strand breaks and has genotoxic effects on both natural and recombinant cytochrome P450 enzymes.</p>

<p>2,4-Dimethyl-3,5-dinitroaniline is a high quality chemical that is used as an intermediate in the synthesis of other compounds. It has been shown to be a useful building block for the synthesis of complex compounds. 2,4-Dimethyl-3,5-dinitroaniline is also a versatile building block and can be used in reactions involving nucleophilic substitution with electron transfer or nucleophilic addition. It has also been shown to be a useful scaffold for a variety of reactions including Friedel-Crafts alkylation and acylation. 2,4-Dimethyl-3,5-dinitroaniline is not available for sale to consumers or retailers.</p>

<p>5-Acetamido-2-nitrobenzoic acid is a metabolic precursor of homarine, which is an important intermediate in the synthesis of pharmaceuticals. 5-Acetamido-2-nitrobenzoic acid is a white crystalline powder that is soluble in water and sparingly soluble in ethanol. It has a molecular weight of 176.1 g/mol and an empirical formula of C7H6NO4P. The compound exists as a zwitterion at neutral pH. The solubility can be increased by adding phosphoric acid or orthophosphoric acid to increase the pH to 3-5, although this may result in the formation of impurities such as orthophosphate or multicolour compounds. 5-Acetamido-2-nitrobenzoic acid is used for the quantitative determination of phosphate in pharmaceutical dosage formulations by regression analysis with multicolour photometry and chromatographic methods.</p>

<p>4-Nitrophthalonitrile is a chemical substance that can be synthesized by the reaction of sodium carbonate with 3,4,5-trimethoxybenzyl alcohol. It can also be prepared using nitro phenol and sodium hydroxide. 4-Nitrophthalonitrile has been shown to have high photochemical activity in the presence of light. The frequency shift of its infrared spectrum is indicative of a nucleophilic addition reaction mechanism. 4-Nitrophthalonitrile has been used as an intermediate for producing other chemicals, such as herbicides and pharmaceuticals.</p>

<p>Methyl 3,5-dinitro-4-hydroxybenzoate is a reactive compound that can be used to glycosylates alcohols. It is a good choice for the glycosylation of complex oligosaccharides due to its high yields and stereoselectivity. Methyl 3,5-dinitro-4-hydroxybenzoate is an efficient method for the synthesis of oligosaccharides. Reaction with methanol and glycosyl acceptor yields a disaccharide in which the two sugars are linked by an alpha-(1,2) glycosidic bond. The nucleophilic nature of methyl 3,5-dinitro-4-hydroxybenzoate allows it to act as a nucleophile in the reaction with the glycosyl acceptor.</p>

<p>2'-Chloro-4'-nitroacetophenone is a reagent that is used in the synthesis of tulobuterol, an oxirane that binds to β2-adrenergic receptors. 2'-Chloro-4'-nitroacetophenone is also used for the synthesis of other drugs, such as benzylated alcohols and phenols. This product has been shown to be metabolized into a number of metabolites, including hydroxybenzyl alcohol and hydroxybenzyl glucuronide.</p>

<p>2-Nitrobenzyl alcohol is a molecule with photochemical properties. It has been used as a solid catalyst and in genotoxic studies. 2-Nitrobenzyl alcohol is also toxic to liver cells, although the mechanism behind this toxicity is not yet clear. The chemical biology of this molecule is being studied, which includes its receptor binding and interactions with human liver cells.</p>

<p>2-Chloro-6-nitroanisole is a versatile building block that can be used to make a variety of products, including pharmaceuticals, agrochemicals, plastics, and other organic compounds. It can be used as a reagent or research chemical in the synthesis of complex molecules, such as synthetic cannabinoids. 2-Chloro-6-nitroanisole is also useful for making high quality compounds and has been used in the synthesis of a number of pharmaceuticals. This compound is an intermediate that can be used to create scaffolds for drug design.</p>

<p>Please enquire for more information about (2-Chlorophenyl)(4-(3-nitrophenyl)(2,5-thiazolyl))amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Methoxy-4-nitrobenzoic acid is a potent and selective inhibitor of aromatase that can be used for the treatment of breast cancer. 3-Methoxy-4-nitrobenzoic acid inhibits the activity of serine proteases, which are enzymes important in protein degradation and cellular signaling. This drug has been shown to inhibit the activity of many other types of kinases, and this makes it a good candidate for use as an anti-cancer agent. 3-Methoxy-4-nitrobenzoic acid also has been shown to inhibit the formation and development of brain tumors when administered via whole body or brain uptake techniques. In addition to inhibiting tumor growth, this drug can prevent metastasis by preventing circulating tumor cells from entering new tissues. The inhibition of estrogen synthesis by 3methoxy-4 nitrobenzoic acid leads to breast cancer cell death in vitro and in vivo.</p>

<p>2-Methoxy-5-nitroaniline is a nitro compound that is cytotoxic at high doses. It is a diazonium salt that can be synthesised from hydrochloric acid and nitrous acid. The toxicity of 2-methoxy-5-nitroaniline has been tested in rats and found to have significant cytotoxicity at doses of 5000 mg/kg, with a LD50 of 2700 mg/kg. The chemical structure of 2-methoxy-5-nitroaniline consists of an amine group, two nitro groups, and two methyl groups. This compound can be synthesized by reacting ammonia with formaldehyde in the presence of nitric acid. 2-Methoxy-5-nitroaniline has shown to inhibit transcription polymerase chain reactions (PCR) in mouse erythrocytes at concentrations as low as 0.1 mM. Dietary</p>

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<p>1-Methyl-2-nitro-3-(tetrahydrofuran-3-yl)methyl)guanidine (1MNTG) is a pesticide that is used to control pests. It has been shown to be highly resistant to degradation by cytochrome P450, which may cause chronic exposure and/or analytical problems. 1MNTG has also been shown to cause genetic damage in bacteria, as well as enzyme activities in the liver and kidneys of rats exposed for short periods of time. 1MNTG has been shown to be an agonist of toll-like receptor 4, which can lead to health effects such as inflammation and have been shown to affect biochemical processes in vitro.</p>

<p>4-Methoxy-2-nitroacetanilide is a byproduct of the manufacture of 4-methoxyacetanilide, which is used in the production of analgesics. It has been shown to be an environmental pollutant that is toxic to animals and plants. The toxicity of 4-methoxy-2-nitroacetanilide is due to its ability to react with amines and form nitrosamines. The rate of acetylation is determined by the kinetics of the reaction, while substituent effects on the molecule determine its reactivity as an electrophile.</p>

<p>4-(Acetylamino)-3-nitrobenzoic acid (AANBA) is a molecule that inhibits the growth of Mycobacterium tuberculosis and influenza virus. It has been shown to have tuberculostatic activity and is able to adsorb to the cavity of the enzyme protein, preventing access by other molecules. AANBA also has antiviral properties that may be due to its ability to inhibit viral particles from binding with a cell surface receptor or inhibiting the synthesis of viral proteins. AANBA binds to the chloride ion in order to maintain the negative charge of the molecule, which is crucial for its antiviral activity.</p>

<p>Please enquire for more information about L-Glutamic acid gamma-(p-nitroanilide) hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromo-2-nitroethanol is a chemical reagent that has the hydroxyl group. It is a site specific biocide, which is used to kill bacteria. 2-Bromo-2-nitroethanol has bactericidal activity against gram negative and gram positive bacteria. It can be used as a preservative in food and pharmaceutical products. This chemical is also effective for killing bacteria in water and wastewater treatment plants. 2-Bromo-2-nitroethanol is applied to surfaces by spraying or dipping, or it can be added to water at concentrations of 0.5 ppm or higher. 2-Bromo-2-nitroethanol can also be used to treat textiles, paper, leather, and rubber products by dipping or spraying these materials with the chemical solution containing 2% concentration of 2-bromo-2 nitroethanol in an aqueous solution of sodium hydroxide (0.5</p>

<p>4-(Bromodifluoromethoxy)Nitrobenzene is a versatile building block that can be used to synthesize a wide variety of organic and inorganic compounds. It is a brominated derivative of nitrobenzene, which is useful for the synthesis of complex compounds and research chemicals. 4-(Bromodifluoromethoxy)Nitrobenzene is also an intermediate for the synthesis of pharmaceuticals and other valuable chemical compounds. This compound has been shown to provide high quality results in reactions with other molecules. 4-(Bromodifluoromethoxy)Nitrobenzene can be used as a scaffold for the construction of more complex molecules.</p>

<p>2-Chloro-5-nitrocinnamic acid is a plant growth regulator that inhibits the root development of plants by interfering with the synthesis of 3-chlorocinnamic acid, which is a precursor in the biosynthesis of lignin. 2-Chloro-5-nitrocinnamic acid inhibits the enzyme cinnamoyl CoA reductase, which catalyzes the first step in this biosynthetic pathway. This compound also has shown to be a strong inhibitor of ester derivatives and pesticides, such as carbaryl and dichlorvos.</p>

<p>1-(3,4,5-Trimethoxyphenyl)-2-nitropropene is a high quality chemical that is a reagent and useful intermediate. It has been shown to be a useful scaffold for the synthesis of various compounds and as a building block for the synthesis of speciality chemicals. This compound can be used in research and as a versatile building block in organic chemistry.</p>

<p>C2'-Chloro-2-(4-nitrophenyl)cinnamonitrile is a fine chemical that is used as a reagent and building block in the synthesis of other compounds. C2'-Chloro-2-(4-nitrophenyl)cinnamonitrile has been shown to react with various reagents to form useful intermediates and speciality chemicals. It can be used as a versatile building block in the synthesis of complex compounds.</p>

<p>2-Fluoro-5-nitrobenzotrifluoride is a chiral, fluorinated organic compound that has been shown to be an effective antiviral agent. It is active against Coxsackievirus B3 and other viruses in vitro. The antiviral activity of 2-fluoro-5-nitrobenzotrifluoride appears to be due to its ability to inhibit the virus's ability to bind and enter the host cell. In vivo studies have shown that 2-fluoro-5-nitrobenzotrifluoride can reduce the spread of coxsackievirus B3 in mice. This compound also has been shown to inhibit viral replication by preventing the synthesis of viral protein pai-1, which is necessary for viral assembly and release from infected cells.</p>

<p>1-(3-Methoxyphenyl)-2-nitroethane, also known as methyl isothiouronium chloride, is a chloride that can be used as an organocatalyst. It is able to catalyze the coupling of nitroalkanes with nitroalkenes in high yields and chemoselectivity, making it a valuable reagent for organic synthesis. 1-(3-Methoxyphenyl)-2-nitroethane can also be used for the preparation of conjugated dienes via the reaction of nitroalkenes with alkenes in the presence of base. This compound is easily recovered by distillation.</p>

<p>2-Bromo-5-cyanonitrobenzene is a chemical compound that has been shown to have broad-spectrum activity against drug-resistant bacteria. It is able to kill gram-negative and gram-positive bacteria, including drug-resistant strains. The mechanism of action for 2-bromo-5-cyanonitrobenzene is not well understood but it has been observed that the molecule undergoes an oxidative cyclization reaction in the presence of chloride ions or hydroxides. This process leads to the formation of a nitrosobenzene metabolite which reacts with DNA to inhibit protein synthesis and cause cell death. 2-Bromo-5-cyanonitrobenzene has also been shown to be potent against a wide range of different types of bacteria, including those most commonly associated with skin infections, respiratory tract infections, and urinary tract infections.</p>

<p>2,4-Dichloro-3-nitrophenol is a synthetic chemical that is used as an intermediate in the synthesis of chloroamines. It is a derivative of phenol and has a chlorine atom on the 2 position. The alcohol group on the 4 position and the chlorine atom on the 3 position are both substituted with chlorine atoms. 2,4-Dichloro-3-nitrophenol has been shown to be effective for the synthesis of chloroamines resistant to nitro groups. This chemical has been shown to be resistant to amines and thus can be used for immobilization purposes. Furthermore, it can be used as an intermediate for chemists who work with organic chemistry due to its ability to undergo reactions with alcohols and phenols.</p>

<p>3,4-Dimethoxy-6-nitrobenzaldehyde is a chemical compound that has been synthesized by the reaction of 3,4-dimethoxybenzaldehyde and nitric acid. The asymmetric synthesis of 3,4-Dimethoxy-6-nitrobenzaldehyde starts with the preparation of the corresponding ester, which is then reacted with nitric acid to produce the desired product. The chemical structure of 3,4-Dimethoxy-6-nitrobenzaldehyde consists of three aromatic rings: a benzene ring fused to a phenyl ring and a pyridine ring. This chemical can be used as an intermediate in the synthesis of epidermal growth factor (EGF). It also has been shown to bind to toll like receptor 4 (TLR4), which activates NFκB signaling pathway and induces apoptosis in monocytes.</p>

<p>2,5-Dimethylnitrobenzene is a glyoxal compound that can be used as an antifreeze or as a solvent. 2,5-Dimethylnitrobenzene is also a byproduct of the reaction between benzyl esters and deuterium isotope. The reactivity of 2,5-dimethylnitrobenzene has been studied in detail using techniques such as anhydrous sodium and fatty acid to activate it. It has also been shown to produce nitrous oxide when reacted with nitric acid in deionized water. The effects of the deuterium isotope have been studied on the reaction rate of 2,5-dimethylnitrobenzene with various chemicals.</p>

<p>4,8-Dichloro-1,5-dinitronaphthalene is a versatile building block that can be used in the synthesis of complex compounds. It is also used as a reagent, speciality chemical, and useful scaffold in research. This compound has been shown to be useful in the synthesis of many different types of products including pharmaceuticals, agrochemicals, polymer intermediates, and other fine chemicals. 4,8-Dichloro-1,5-dinitronaphthalene is a high quality chemical with a purity level of 98%.</p>

<p>Sodium nitroprusside dihydrate is an oxygen transport agent that works by inhibiting the enzyme cyclase. This inhibits the production of tnf-α and other inflammatory mediators, which reduces inflammation and pain. Sodium nitroprusside dihydrate is used to lower blood pressure in emergency situations, such as shock. It has been shown to be effective for treating pulmonary hypertension, chronic obstructive pulmonary disease, and other conditions related to oxygen transport. Sodium nitroprusside dihydrate is a metastable molecule that can be converted into a stable form (sodium nitroprusside) by ester hydrochloride or fatty acid esters.</p>

<p>Methyl 3-chloro-2-nitrobenzoate is an organic compound that has been used in a variety of cross-coupling reactions. It is a useful reagent for the synthesis of amides, esters, and nitriles. Methyl 3-chloro-2-nitrobenzoate has also been used as a ligand in biomimetic studies and crystallographic analyses. The electron density maps obtained from x-ray crystallographic studies of methyl 3-chloro-2-nitrobenzoate have shown nitrogen atoms at the position 2 and 4 on the ring. This information was used to predict the electron density map for methyl 3,5 dichloro 2 nitro benzoate with nitrogen atoms at positions 2 and 5 on the ring.</p>

<p>N-alpha-[2,4-Dinitro-5-fluorophenyl]-L-valine amide is an acidic amino acid that is used as a reagent in organic synthesis. It has been shown to have amide and hydrogen bond properties. This compound has been shown to be involved in the biosynthesis of carboxylic acids and primary amino acids. It also absorbs UV light at 265 nm and can be used for determination of uv absorption using high performance liquid chromatography (HPLC).</p>

<p>2-Fluoro-6-nitrobenzaldehyde is an electron donor that reduces a range of electron acceptors including piperazine. This compound has been shown to have antitumor effects. 2-Fluoro-6-nitrobenzaldehyde has also been shown to inhibit the growth of cancer cells in vitro and in vivo. The mechanism of action is not yet known, but it is thought that 2-fluoro-6-nitrobenzaldehyde may be a potential chemotherapeutic agent for pancreatic cancer therapy.</p>

<p>4-Fluoro-3-nitroanisole is a useful chemical intermediate and building block. It is a versatile compound that can be used in research as well as commercial applications. 4-Fluoro-3-nitroanisole has the CAS number 61324-93-4. This chemical is often used in the synthesis of complex compounds, such as pharmaceuticals, pesticides, and fragrances. The high quality of this product makes it a good reagent for laboratory experiments.</p>

<p>4-Methyl-3-nitrobenzaldehyde is an aldehyde that is synthesized in vitro and used as a replication inhibitor. It has been shown to inhibit the replication of dsDNA, ssDNA, and RNA viruses. 4-Methyl-3-nitrobenzaldehyde binds to nucleic acids by forming hydrogen bonds with the carboxylic acid group on the molecule and the acceptor, which are usually hydroxyl groups or amino groups. 4-Methyl-3-nitrobenzaldehyde can be used for the synthesis of viologens, which are molecules that can be used as electron acceptors in organic reactions.</p>

<p>3-Methyl-4-nitro-N-acetylbenzeneamine is a biodegradable chemical that acts as an inhibitor of the growth rate of bacteria in wastewater treatment. It has been shown to be effective in both aerobic and anaerobic environments. 3-Methyl-4-nitro-N-acetylbenzeneamine is a racemic mixture, consisting of two isomers that are easily separated by chromatography. The primary mechanism for degradation of this chemical is acetylation, which converts it into acetic acid and methyl acetate. 3-Methyl-4-nitro-N-acetylbenzeneamine can also be degraded by aerobic soil bacteria with the help of fatty acids. This chemical is not toxic to humans or animals and does not affect crop plants.br&gt;</p>

<p>2-Chloro-6-nitrobenzyl alcohol is a versatile building block that is used as a reactant in chemical synthesis. It is used to synthesize other compounds, such as pharmaceuticals and pesticides. This compound can also be used as an intermediate or scaffold in the synthesis of more complex compounds. 2-Chloro-6-nitrobenzyl alcohol has been shown to have a high quality and is useful for research purposes. It can be used in the production of fine chemicals, useful building blocks, and reagents.</p>

<p>1-Bromo-3-fluoro-2-nitrobenzene is the target compound in this reaction. The starting materials are triethylamine, trichloride and ethyl alcohol. The reagents are mixed at a high temperature to produce the target product. This procedure can be scaled up for large-scale production using hydrazine as a solvent.</p>

<p>Ethyl 4-cyano-3-nitrobenzoate is a chemical compound with the structural formula of CHNO. It is a building block for organic synthesis and can be used in the production of high quality research chemicals and speciality chemicals. Ethyl 4-cyano-3-nitrobenzoate has been shown to react with a variety of amines to form urea derivatives that are useful as versatile building blocks or complex compounds. This reagent is also useful as an intermediate in the synthesis of various pharmaceuticals. CAS No. 321162-58-7</p>

<p>4-Amino-3,5-dinitrobenzoic acid (4ADBA) is a reactive chemical compound with acidic properties. It reacts with nucleophiles to form diazo compounds, which are used in analytical methods for the detection of amines and phenols. 4ADBA can be used to measure the concentration of aspirin in pharmaceutical formulations. The reaction is linear over a wide range of concentrations and has an optimal reaction time of 10 minutes at pH 2.0–2.5. The half-life values for 4ADBA are approximately 3 hours at pH 3 and 7 hours at pH 5.</p>

<p>2-Chloro-3-nitrobenzoic acid ethyl ester is a reactive chemical intermediate that can be used as a building block in organic synthesis. It is a versatile reagent that can be used in many reactions, such as condensation, cyclization, amination, and oxidation. The compound has been shown to be useful in the synthesis of polymers, pharmaceuticals, and natural products. 2-Chloro-3-nitrobenzoic acid ethyl ester is an environmentally friendly compound with a low toxicity profile. It has been classified as a high quality fine chemical with CAS number 3979-45-1.</p>

<p>1-Bromo-3,4-dimethoxy-6-nitrobenzene is a pharmacological agent that has been used as a catalyst and cleavable complex. It can be used to synthesize melamine, anilines and other moieties. The 1,2,3-triazole ring of the molecule is modified by substitution with nitroarenes or nitrobenzene to form a protoberberine alkaloid. This chemical compound has been shown to be a competitive inhibitor of topoisomerase I with an IC50 value of 0.2μM in calf thymus DNA gyrase assays. It also has thermal stability up to 90°C for at least 24 hours when treated with phenol and chloroform for purification purposes.</p>

<p>Ethyl (4-nitrophenyl)acetate is a molecule that has been used in biological studies as an active substance for its antibacterial properties. It has been shown to have minimal inhibitory concentration (MIC) of 0.5 µg/mL against gram-positive bacteria and 1 µg/mL against gram-negative bacteria. The molecule is also the main active methylene in the ethyl ester. It can be found in coumarin derivatives, which are natural products derived from plants of the genus Coumaroua. The molecule is nucleophilic and can react with other molecules through a number of different mechanisms, such as by adding or removing hydrogen atoms to the molecule. This reaction is called a substitution reaction, and it is an important technique for pharmacokinetic properties.</p>

<p>1-(3-Pyridinyl)cyclopropanamine bis-4-nitrobenzoate salt is a fine chemical that is used as a versatile building block in the synthesis of complex compounds. It is also used as a reagent or speciality chemical in research, and to make useful building blocks and intermediates. 1-(3-Pyridinyl)cyclopropanamine bis-4-nitrobenzoate salt is a useful scaffold for the synthesis of compounds with biological activity.</p>

<p>2-Nitroethanol is a chemical compound that is used as an antioxidant, antimicrobial preservative, and flavoring agent in foods. It can be synthesized in an asymmetric synthesis reaction, which involves the addition of a nitro group to one of the two carbons in ethylene glycol. The toxicity profile of 2-nitroethanol has not been extensively studied, but it appears to have low toxicity based on animal studies. A number of inhibitory compounds have been identified for 2-nitroethanol, including benzalkonium chloride and propionate. The inhibitory effects of 2-nitroethanol are concentration dependent and may be due to hydrogen bonding with proteins or intramolecular hydrogen transfer reactions with other molecules. Inhibition of viral replication by 2-nitroethanol has been observed in influenza virus and human immunodeficiency virus (HIV) studies. This inhibition may be due to alterations in fatty acid metabolism or changes in the</p>

<p>2,3-Difluoro-4-nitroanisole is a chemical compound with CAS No. 66684-59-1. It is a useful intermediate that can be used to synthesize other chemicals and compounds. 2,3-Difluoro-4-nitroanisole can be used for the synthesis of research chemicals and speciality chemicals. This compound has been found to be a versatile building block that can be used in many reactions as a reagent. 2,3-Difluoro-4-nitroanisole has high quality and is a fine chemical with many uses.</p>

<p>3,5-Dinitro-4-hydroxyphenylpropionic acid hydrazide is a versatile building block that can be used in the synthesis of complex compounds. It is an intermediate for the production of research chemicals and reagents, as well as a useful scaffold for making new compounds. This compound has been shown to be stable in air and water and is not toxic when ingested. 3,5-Dinitro-4-hydroxyphenylpropionic acid hydrazide is also soluble in many organic solvents and has low volatility.</p>

<p>Please enquire for more information about 3-(tert-butyl)-1-(4-nitrophenyl)indeno[2,3-d]pyrazol-4-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Nitroresorcinol is a hydroxamic acid that inhibits bacterial growth by reacting with riboflavin, which is essential for the synthesis of flavoproteins and folate. This compound has been shown to have a specific growth rate on the order of 10^-5 and 10^-6 M. The reaction of 4-Nitroresorcinol with riboflavin leads to the production of nitric oxide and hydrogen peroxide, which can lead to the destruction of cells. 4-Nitroresorcinol has been synthesized in an organic solvent using various techniques such as thermal decomposition, photochemical synthesis, and hydrolysis. 4-Nitroresorcinol can be viewed under a microscope using techniques such as electron microscopy or light microscopy.</p>

<p>Please enquire for more information about 3-(tert-butyl)-4-(3-(4-nitrophenyl)prop-2-enylidene)-1-phenyl-2-pyrazolin-5-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Nitrobenzaldehyde oxime is a phenylhydrazone derivative that is a potent cytotoxic agent. The 1,2-nitration of the benzene ring in 4-nitrobenzaldehyde oxime produces a reactive intermediate that reacts with nucleophilic groups on cellular macromolecules to produce DNA strand breaks and other types of damage. 4-Nitrobenzaldehyde oxime has been shown to have significant anticancer activity against leukemia cells in culture, as well as antibacterial and anticancer activity against Staphylococcus aureus and Escherichia coli.</p>

<p>Ethyl 4-fluoro-3-nitrobenzoate is a molecule that has been shown to have significant cytotoxicity and antiproliferative activities against cancer cells. It has been shown to inhibit the replication of RNA in replicon cells, which is an assay used to measure the ability of a drug to inhibit viral replication. The molecule also has significant anticholinesterase activity, which may be due to its hydrogen bond interactions with choline esters.</p>

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

<p>3-Nitrobenzyl alcohol is a low potency drug that is used for the treatment of cancer. It is a derivative of trifluoroacetic acid, which has been shown to have anti-tumor effects in animals. 3-Nitrobenzyl alcohol binds to the matrix on the surface of cells by hydrogen bonding and forms an intramolecular hydrogen bond with the nitrogen atom. This process leads to increased fluorescence intensity, which can be detected using matrix-assisted laser desorption ionization mass spectrometry (MALDI MS). The fatty acid group found in 3-nitrobenzyl alcohol increases its solubility in water and facilitates penetration into lipid bilayers. This compound exhibits cytotoxicity against monoclonal antibody-positive B cell lymphoma cells and may also have anti-inflammatory properties due to its inhibition of picolinic acid synthesis.</p>

<p>Beta-nitroisomyristicin is a chemical building block that is used in the synthesis of various compounds. It is a versatile intermediate that can be used in many organic syntheses, such as the synthesis of fine chemicals and pharmaceuticals. Beta-nitroisomyristicin is a high quality reagent for research, which can be used to make other compounds for use in research or commercial purposes.</p>

<p>(E)-b-Nitrostyrene is a nitro compound that is used as a precursor in the synthesis of teicoplanin. (E)-b-Nitrostyrene is synthesized by the reaction of sodium carbonate with cationic surfactant, which produces an intermediate. This intermediate then undergoes a cycloaddition process with nitric oxide to produce (E)-b-nitrostyrene and water. The redox potentials of this compound are determined using kinetic data. The structural analysis of b-nitrostyrene includes NMR and FTIR spectra, which reveal that it has one asymmetric center. It was found that b-nitrostyrene has apoptotic effects on human macrophages in vitro.</p>

<p>2-(4-Nitrophenoxy)ethanol (NPEO) is a water soluble, synthetic compound that has been shown to have anti-tumor properties. NPEO was found to be toxic to tumor cells in vitro and inhibits the growth of tumor cells in vivo. NPEO also inhibits the synthesis of DNA and RNA, which are important for cell division. This inhibitory effect may lead to the death of cancer cells by interfering with their ability to grow and divide.</p>