Nitro

3-Nitroacetanilide is a molecule that is found in the testes. It is a structural analog of acetanilide and has been shown to have similar biological function as acetanilide in inhibiting prostaglandin synthesis. 3-Nitroacetanilide has been shown to inhibit the production of prostaglandin E2 by inhibiting cyclooxygenase (COX) enzyme activity. 3-Nitroacetanilide is synthesized by reacting hydrochloric acid with an acetamide derivative, such as ethanolamine or acetamide hydrochloride, in the presence of sodium carbonate and anhydrous sodium. The reaction takes place in a model system at pH 8.0 and room temperature. A cycle analysis identifies the number of steps necessary for this reaction to take place. The molecular weight of 3-nitroacetanilide can be determined by gravimetric analysis which involves weighing out a sample and then

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4-Bromo-2-fluoro-5-nitrotoluene is a chemical building block that is used as a research and speciality chemical. It has been shown to be useful in the synthesis of complex compounds, including pharmaceuticals and dyes. 4-Bromo-2-fluoro-5-nitrotoluene is also used as a reagent for the reaction with other chemicals, such as thiourea, to form 2,4,6-trichlorophenylacetonitrile. This compound is classified as hazardous by the American Chemical Society (ACS) because it can cause irritation to the skin and eyes.

Applications 4-Hydrazino-7-nitrobenzofurazane (cas# 90421-78-6) is a useful research chemical.

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5-Nitro-1,3-benzoxazol-2(3H)-one is a molecule that belongs to the class of piperazines. It has been shown that this molecule inhibits growth in test organisms such as bacteria and insects. The inhibitory properties of 5-Nitro-1,3-benzoxazol-2(3H)-one are due to its nucleophilic nature. This molecule also has low activity against phenolic compounds and is not active against nucleophile reactions. The nitro group on this molecule may be responsible for its growth inhibitory activity.

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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.

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1-Bromo-3,5-dinitrobenzene is an optical probe that has been used in reaction systems to study the reactivity of nucleophiles. The fluorescence of 1-bromo-3,5-dinitrobenzene changes with the nature of the nucleophile and its concentration. This molecule is unreactive with other molecules and can be used as a drug development tool. The centroid of 1-bromo-3,5-dinitrobenzene is constant at 298 K. Crystals for 1-bromo-3,5-dinitrobenzene have been analyzed by XRD and FTIR.

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4,4'-Dinitrodiphenyl ether is a chemical that is used to produce dyes and explosives. It reacts with anhydrous sodium at a constant temperature in a reaction vessel to form diphenyl ethers. The rate of this reaction can be enhanced by adding water vapor or organic solvents. This chemical is toxic and can cause circulatory system damage if inhaled or ingested. 4,4'-Dinitrodiphenyl ether may also be found in the environment as a result of industrial pollution or spills.

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Z-L-leucine 4-nitrophenyl ester is a non-natural amino acid. It is a competitive trypsin inhibitor that has been shown to inhibit the proteolytic activity of trypsin, chymotrypsin, and elastase. The kinetic parameters for this inhibitor are similar to those of natural substrates and inhibitors. Z-L-leucine 4-nitrophenyl ester binds reversibly to the active site of these enzymes, which prevents hydrolysis of protein substrates. This inhibition is reversible, as the enzyme can reactivate when the inhibitor is removed from the active site. Z-L-leucine 4-nitrophenyl ester has been shown to be a potent inhibitor of proteinase activity in various tissues and cell cultures derived from animals and humans.

4-Nitropyrazole is a nitrogen-containing heterocyclic compound. It has a molecular weight of 148.14 and a melting point of 112.5 degrees Celsius, as well as an observed boiling point of 183 degrees Celsius. 4-Nitropyrazole has been shown to interact with hydrogen bonds, forming a hydrogen bond with the amide group of proteins. This interaction is believed to be responsible for the solubility data that shows this molecule to be soluble in water and polar organic solvents but insoluble in nonpolar organic solvents such as benzene or hexane. 4-Nitropyrazole has been shown to have vibrational and proton NMR spectra that are consistent with its molecular formula C4N3O2N. The proton spectrum displays singlets at positions 2.01 ppm and 3.67 ppm, indicating the presence of one proton on each carbon atom in the ring system (C1=H). The vibr

4-Chloro-2-nitrobenzaldehyde is a reactive intermediate that has been used to investigate the reaction mechanism of protonation. It is an n-oxide and has been shown to react with calcium carbonate under acidic conditions, forming a stable product. 4-Chloro-2-nitrobenzaldehyde has also been used in the synthesis of amides and nitro compounds. This compound possesses two functional groups, which are a nitro group and a chloro group on the aromatic ring.

4'-Butoxy-beta-methyl-beta-nitrostyrene is a fine chemical that has been used as a reagent and a building block. It is an intermediate of various complex compounds and has been used in the synthesis of other high quality products. 4'-Butoxy-beta-methyl-beta-nitrostyrene can be used as a building block to make speciality chemicals, research chemicals, or versatile building blocks which may be useful for reactions.

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5-(4-Nitrophenyl)isoxazole-3-carboxylic acid is a synthetic, organic solvent that has been used in the synthesis of hydroxybenzoic acid and piperazine. 5-(4-Nitrophenyl)isoxazole-3-carboxylic acid can be prepared by reacting the orthophosphoric acid with benzoic anhydride in an organic solvent such as chloroform. 5-(4-Nitrophenyl)isoxazole-3-carboxylic acid is a white, crystalline solid that melts at 125 °C. It has been shown to be resistant to radiation, but not to aliphatic hydrocarbons.

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. 2-Benzyloxy-6-nitrotoluene reacts with formamide in the presence of catalytic amounts of acid to give 2-[2-(benzyloxy)ethoxy]benzonitrile, which can be converted to 2-[2-(benzyloxy)ethoxy]pyrrolidine by heating with pyrrolidine. 2-[2-(Benzyloxy)ethoxy]pyrrolidine can then be used for synthesis of various drugs such as 4-benzyloxypiperidines, 4-benzyloxypiperidones and benzodiazepines. The keyword search "pyrrolidine" finds this compound

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2-Bromo-5-nitropyrazine is a pyridine derivative that is synthesized by the Diels-Alder reaction of 2,4-dinitrochlorobenzene and 2,6-bis(diethylamino)pyridine. This compound has been shown to have intramolecular electron donation properties in its side chain. The electron donating nature of this compound may be due to its intramolecular diels-alder reactions with electron donating groups such as pyrazines.

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3-Nitrobenzamidine hydrochloride is a switchable and tunable synthetic heterocyclic guanidine. It has been shown to have biologically activity in the form of nucleotide exchange and DNA cleavage with adenosine, guanosine, cytosine, and thymine. 3-Nitrobenzamidine hydrochloride belongs to the family of 3-nitrobenzamidines. This compound has been shown to be a suitable scaffold for the reshaping of families such as benzimidazoles or guanidines.

Ethyl 5-Nitroindole-2-Carboxylate is a precursor to the anti-HIV drug Delavirdine. It is synthesized by condensation of ethyl pyruvate and urea derivative in the presence of thionyl chloride. This compound can be used as an intermediate in the synthesis of other compounds such as ethyl ester and ethyl pyruvate. The chemical reaction is carried out at room temperature using a chlorinated solvent such as methylene chloride or chloroform. Ethyl 5-nitroindole-2-carboxylate can also be used for the synthesis of other drugs, including antitumor agents.

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5-(4-Methylpiperazin-1-yl)-2-nitrophenyl]amine is a potential agent for the treatment of benzene poisoning. It has been shown to be an irreversible inhibitor of the enzyme dihydrofolate reductase, which plays a role in the synthesis of DNA and proteins. 5-(4-Methylpiperazin-1-yl)-2-nitrophenyl]amine reversibly inhibits methylamine dehydrogenase (EC 1.4.1.3) with a Ki value of 0.8 mM and also inhibits pyridoxal phosphate dependent aminotransferases, including alanine aminotransferase (EC 2.6.1.2), aspartate aminotransferase (EC 2.6.1.1), and glycine aminotransferase (EC 2.6.1.19). The inhibition of these enzymes

5-Nitro nicotinic acid is a drug that has been synthesized in the laboratory. It is a white crystalline solid with a molecular weight of 201.18, and it has the chemical formula of C6H5NO2. 5-Nitro nicotinic acid is an antitubercular drug that inhibits Mycobacterium tuberculosis and Mycobacterium avium complex without inhibiting other human cells. It also inhibits the growth of bacteria that are resistant to aminoglycosides (e.g., Pbtz169). This drug binds to the enzyme NADH dehydrogenase, which leads to inhibition of bacterial respiration and ATP synthesis. 5-Nitro nicotinic acid also has antimycobacterial activity against mycobacteria by forming nitric oxide radicals (NO) through hydrogen peroxide oxidation, which react with cellular components such as DNA and proteins.

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3-(2-Nitrophenyl)oxiran-2-yl](phenyl)methanone is a crystalline product with a molecular weight of 284.59. It has been synthesised from the reaction of 5-hydroxy-2-nitrobenzaldehyde and sodium carbonate in the presence of chloride. 3-(2-Nitrophenyl)oxiran-2-yl](phenyl)methanone has shown degradative properties, as well as spectroscopic studies that suggest its mechanism of action may involve hydrogen chloride and an n-oxide intermediate.

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Applications 1,5-Dinitroanthraquinone 97% (cas# 82-35-9) is a useful research chemical.

2,5-Dibromo-4-methyl-3-nitropyridine is a pyridine derivative that is synthesized by reductive amination of 2,5-dibromo-4-methylpyrrole with aniline. It has been used in the synthesis of pharmaceuticals and chemical intermediates. The synthesis of this compound is scalable and can be used to produce large quantities of product. In addition, this compound has been used in the discovery of drugs for a variety of diseases including cancer.

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4-N-Hexyloxynitrobenzene is a hydrophobic, colorless liquid that is soluble in ether and slightly soluble in water. It has an equilibrium constant of 2.2 at 25°C, pK a of 4.6, and pK b of 11.5. The reaction with p-nitrophenyl gives a hydroxyphenyl compound with the ether group replaced by hexyl. 4-N-Hexyloxynitrobenzene can be used as a solvent for nitrocellulose or other cellulose esters, and as an additive to plasticizers such as dioctyl phthalate.

2-Nitrobenzene-1,4-diol is an organic compound with the formula HOCH2NO2. It is a yellow solid that is soluble in water, ethanol and ether. 2-Nitrobenzene-1,4-diol reacts with hydrogen fluoride to produce a polymer film containing nitro groups. This reaction mechanism can also be applied to other nitro compounds. The reaction products of this process are nitrogen atoms and a particle. The rate constant for this reaction has been shown to be second order. 2-Nitrobenzene-1,4-diol is found in fatty acids and regiospecifically reacts with human liver cells.

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2-Hydroxy-5-methoxy-3-nitrobenzaldehyde is a 6-membered aromatic compound that has been shown to have anti-cancer properties. It has been shown to inhibit the proliferation of cancer cells by inhibiting protein synthesis, as well as inducing apoptosis. This compound also inhibits the growth of colon cancer cells and cervical cancer cells in culture. 2-Hydroxy-5-methoxy-3-nitrobenzaldehyde has an inhibitory effect on the growth of cancer cells and may be used for treatment against tumors.

2-(2-Fluoro-5-nitrophenyl)acetic acid is an organic compound that has been synthesized by intramolecular cyclization of a 2-fluoroalkyl acetonitrile with an azide. The molecule has the general formula of RC(O)N=NOH, where R represents the alkyl group and the nitro group is attached to the carbon atom. This process involves two elimination reactions, one reaction in which a water molecule is eliminated and a second reaction in which a molecule of ammonia is eliminated. The macrocyclic ring features two betaine groups (ROCONH). These are found in many naturally occurring compounds such as asparagine, and azides. The conformation of this molecule was simulated using molecular dynamics simulations. It has been hypothesized that it will have anti-inflammatory properties due to its macrocyclic structure and its ability to bind to proteins and inhibit protein synthesis.

Applications 4,5-DIMETHOXY-2-NITROBENZAMIDE (cas# 4959-60-8) is a useful research chemical.

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

4-Chloro-8-nitroquinoline is a postulated carcinogen that has been shown to cause cancer in animals. It has also been shown to induce skin cancer in humans. 4-Chloro-8-nitroquinoline is a nucleophile that reacts with DNA, RNA and proteins by forming covalent bonds. In addition, this chemical can react with nitrous acid to form reactive intermediates that may bind to DNA and cause mutations. Analysis of the absorption spectra of this compound shows a strong peak at 285 nm, which is consistent with the nitro group. The technique of nuclear magnetic resonance (NMR) was used to analyze diploid cells for the presence of 4-chloro-8-nitroquinoline and found a concentration of 0.1 mM. This analysis suggests that this chemical binds preferentially to DNA and causes mutations in diploid cells.

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2-Nitrothiophene-4-carboxylic acid is a nitro compound that is used as a chemotherapeutic agent. It has been shown to have affinity for DNA and inhibits the synthesis of nucleic acids, which leads to cell death. This drug is also mutagenic in kinetic assays. The acetylation of 2-nitrothiophene-4-carboxylic acid yields an N-acetyl derivative, which can be hydrolyzed by hydroxylamine to yield a methyl ester. Nitrothiophene-4-carboxylic acid has been shown to be mediated by nitro groups, with substituent effects on the enzyme activity and thermodynamic parameters.

3-Fluoro-5-nitrotoluene is a chemical compound that has a variety of applications as a research and development intermediate, as well as in the manufacture of pharmaceuticals, dyes, and explosives. It is commercially available in both liquid and solid form, and can be used in any number of chemical reactions to create other compounds. 3-Fluoro-5-nitrotoluene is a versatile building block that can be used to make other chemicals. It can also be used to make fine chemicals and complex compounds.

5-Nitrovanillin is a white crystalline solid with a molecular formula of C8H7NO2. It reacts with nucleophilic compounds, such as ammonia, in the presence of heat to produce a molecule containing an oxygen atom and two nitro groups. 5-Nitrovanillin has been found to undergo demethylation when heated in the presence of hydroxylamine. Reaction products include protocatechuic acid, nitromethane, and 5-nitrobenzoic acid. This compound can be identified by its characteristic nmr spectrum that includes a hydroxyl group and a hydrogen bond between the nitrogen atom and the hydroxyl group. The chemical ionization mass spectrometer can also be used to identify 5-nitrovanillin.

2-Methyl-6-nitrobenzothiazole is an electron-withdrawing group that can be used as a probe to monitor the permeability of cell membranes. It is known to react with nucleophiles such as piperidine in a nucleophilic ring opening reaction. 2-Methyl-6-nitrobenzothiazole has been shown to have a linear response when monitoring the fluorescence of cells. This probe is not stable in acidic environments, and will lose its fluorescence if it comes into contact with an acidic solution. 2-Methyl-6-nitrobenzothiazole can also be used as a fluorescent stain for electron microscopy.

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Bis(2,4-dinitrophenyl) acetic acid ethyl ester has the chemical formula C6H5NO3. It is a white crystalline solid that is soluble in water. This compound has been shown to mimic the carbonyl group and react with nucleophiles. It also has an intramolecular electron pair, which forms a covalent bond between atoms and stabilizes the molecule. The crystal structure of bis(2,4-dinitrophenyl) acetic acid ethyl ester consists of alternating double bonds and single bonds. The x-ray diffraction pattern shows that the molecule is symmetrical and has an intramolecular bond.

2-(4-Nitrophenyl)-4,5-dihydro-1,3-oxazole is a nitroarene compound with a phenyl group on the aromatic ring. It has been shown to be an active catalyst for the reduction of sodium borohydride to form sodium borohydride. This reaction can be carried out in a single crystal of the molecule by x-ray diffraction methods. The catalytic activity of 2-(4-Nitrophenyl)-4,5-dihydro-1,3-oxazole is due to its ability to bind two molecules of sodium borohydride simultaneously. The binding site is located near the oxygen atom at the 1 and 3 positions in the aromatic ring. 2-(4-Nitrophenyl)-4,5-dihydro-1,3-oxazole has also been shown to exhibit diffraction properties in a single crystal x ray diffraction experiment

Ethyl 4-amino-3-nitrophenylcarbamate is a nitro compound that is used as a precursor for the synthesis of other nitrogen compounds. It can be synthesized by cyclisation of ethyl 3-nitrobenzoylcarbamate and methylsulphonyl chloride. The product contains an acyl group esterified to the amine group, which reacts with hydrochloric acid to produce an acyl chloride. The acyl chloride then reacts with nitric acid to produce ethyl 4-amino-3-nitrophenylcarbamate. Ethyl 4-amino-3-nitrophenylcarbamate hydrolyses to give an n-oxide, which can be reduced to a primary amine and an amide, or oxidised back to the original carbamic acid.

Stability Moisture Sensitive Applications 4-Isothiocyanato-4'-nitrodiphenyl ether (cas# 19881-18-6) is a useful research chemical. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

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Applications 2,5-Dinitrotoluene, is a building block used in various chemical synthesis. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

3,3'-Dinitro diphenyl disulfide is a sulfa drug that inhibits the growth of bacteria and has been shown to be an effective treatment for cervical cancer. It is a nucleophilic compound that reacts with sulfhydryls on the bacterial cell wall by displacement of the sulfhydryl group. 3,3'-Dinitro diphenyl disulfide also inhibits protein synthesis and DNA replication in bacteria, leading to cell death. This chemical is synergistic with other drugs such as maduramicin ammonium and salinomycin sodium in treating infections caused by tenella. 3,3'-Dinitro diphenyl disulfide binds to the sulfur atom of cysteine residues on proteins in the bacterial cell wall by a nucleophilic substitution reaction. The reaction leads to release of a sulfenic acid or sulfinic acid from cysteine residues, which inhibits cell division.

4-Methyl-3-nitrophenyl isocyanate (4MPN) is a chiral diisocyanate that can be used as an activated diisocyanate. 4MPN is prepared by the carbonylation of 3-nitrobenzaldehyde and xylene with hydrogen chloride in the presence of a catalyst. Impurities, such as chlorides or sulfurs, can be detected using surface methodology techniques. The feedstock for this compound is usually xylene, which has a high boiling point. This product contains reactive functional groups that can be used to modify surfaces and create polyurethane products.

2-Chloro-6-nitroquinoline (CNDQ) is a synthetic compound that is used as an analog of serotonin. This compound has been shown to be a potent and selective serotonin reuptake inhibitor in vivo, with affinities for the serotonin transporter that are more than 100 times greater than other monoamine transporters. CNDQ has also been observed to inhibit the uptake of dopamine and norepinephrine, which may account for its antidepressant activity. The alkyl groups on this molecule enhance its binding affinity for amine receptors.

2-Fluoro-3,5-dinitropyridine is a pyridine derivative that has been shown to have an electron-withdrawing group at 2-position. The functional theory of 2-fluoro-3,5-dinitropyridine shows that the compound has intramolecular hydrogen bonding and yields a resonance structure where the nitrogen atom is protonated. It has been shown to react with alcohols in a similar manner as pyridine. The 2-fluoro substituent also increases the reactivity of the ring by making it unsymmetrical. This means that this compound can be used in synthesis reactions to form methyl derivatives.

5-Nitroisatoic anhydride is a chemical compound that has found use in the synthesis of complex compounds and fine chemicals. It is a useful intermediate for the preparation of 5-nitro-1,2,4-triazole, which can be used as a research chemical or speciality chemical. 5-Nitroisatoic anhydride reacts with alcohols to form nitrosamines. This reaction component is also used in organic syntheses and as a reagent in the production of other chemicals.

4-Methoxy-2-nitrobenzene-1-sulfonyl chloride is an expansion agent that inhibits the activity of matrix metalloproteinases, specifically those involved in inflammation. It is a trisubstituted trifluoroacetic acid with a traceless, solid-phase synthesis to provide a mononuclear blood assay. 4-Methoxy-2-nitrobenzene-1-sulfonyl chloride has been shown to reduce the production of inflammatory cytokines, such as TNFα, by inhibiting the activity of metalloproteinases and their substrates. This agent may be useful for the treatment of inflammatory diseases.