Nitro

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7-Nitro-3,4-dihydro-1H-naphthalen-2-one is a synthetic compound that has been shown to have antimicrobial activity. It is used as a precursor for the synthesis of other compounds such as 7-nitrobenzofurazan and 5,6,7,8-tetrahydronaphtho[2,3-b]furan. The antimicrobial activity of this compound is due to its ability to inhibit bacterial growth by cleaving the bacterial cell wall. This compound also has been shown to be an acetylating agent.

2-Benzoyl-4-nitrobenzoic acid (2BA) is an organic compound that belongs to the carboxylic acid class. It is a white crystalline solid with a melting point of 84.4°C and a density of 1.29 g/cm3. 2BA is an interplanar molecule with two benzoate groups and two nitro groups. The nitro groups are located in the ortho positions, while the carboxylic group is in the meta position. This molecular structure is what gives 2BA its efficiency and high boiling point, as well as its dimerization properties. 2BA has been used in some experiments to produce monoclinic crystals, which have a higher density than other types of crystals. These crystals are more useful for X-ray crystallography because they have a lower index of refraction than other types of crystals such as cubic or tetragonal

Benzyl 4-nitrophenyl carbonate is a synthetic intermediate that is used in the synthesis of aziridines. It can be prepared by acetylation of benzaldehyde with nitroethane, followed by removal of the benzoic acid. It can also be generated from divinylbenzene and aziridine. The material has a melting point of about 160°C and solubility in chloroform, methanol, or carbon tetrachloride. Benzyl 4-nitrophenyl carbonate is typically used as an unsolvated starting material for the synthesis of amines and carboxylic acids.

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3-Nitropyridine-2,6-diol is a cyclizing agent that converts nitropyridine to 3-(1H-imidazol-3-yl)pyridine. It is used in the synthesis of acrylates and sulfuric acid esters. 3-Nitropyridine-2,6-diol can be used as a reagent for cyclizing nitroarenes to form pyridines. The reaction is catalyzed by sulfuric acid and sulfuric acid esters. This compound is also used as a chlorinating reagent in the preparation of alkenes and alkynes.

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Applications Nitrofurate is a useful organic reagent. It is used for preparation of polycyclic small molecules. References Tan, D., et al.: J. Am. Chem. Soc., 121, 9073 (1999); Lu, P., et al.: Org. Lett., 11, 5710 (2009);

2-Nitroisonicotinic acid is a 4-amino-3-pyridinecarboxylic acid. It has been shown to be an effective inhibitor of the enzyme nitric oxide synthase in a number of different species, including rats and humans. 2-Nitroisonicotinic acid can be used as a starting material for the synthesis of other biologically active compounds.

3'-Fluoro-2'-hydroxy-beta-methyl-beta-nitrostyrene is a fine chemical with a CAS No. 1017060-19-3. It is an intermediate that can be used in the synthesis of complex compounds and research chemicals. This product also has high purity and quality, making it a versatile building block for speciality chemicals. 3'-Fluoro-2'-hydroxy-beta-methyl-beta-nitrostyrene is useful as a reaction component in the synthesis of many other chemical compounds.

2-Nitrophenyl diphenylamine (2NPD) is a nitro compound with a nitrogen atom. 2NPD can be used as an electron donor for organic synthesis and has been extensively used in the study of the interaction between nitro compounds and other molecules. The ground state geometry of 2NPD was calculated using quantum chemical methods, which showed that the molecule has one planar configuration with four axial bonds and two equatorial bonds. It can form a resonance structure through interactions between the lone pair of electrons on the nitrogen atom and the π* orbital on the carbon atom. This resonance structure gives rise to two possible geometries, both of which are linearly symmetric. Substituent effects on 2NPD have been studied by comparing its spectroscopic properties with those of methoxy substituted 2NPD. Methoxy substitution has been shown to reduce the frequency of vibration and alter some vibrational modes, as well as affect electronic properties such as ionization

2-Isothiocyanato-1-methoxy-4-nitrobenzene (ITCMB) is a cytotoxic compound with anticancer activity. It is a potent inhibitor of DNA synthesis and cell division, which leads to apoptosis and tumor regression. ITCMB induces cell cycle arrest at the G2/M phase and induces apoptosis in human tumor cells. The mechanism of action of this compound is not yet known, but it may be due to its ability to block the DNA replication machinery in the cancer cells. ITCMB has been shown to inhibit proliferation of human tumor cell lines in vitro and cytotoxicity studies are being conducted in vivo.

4-Fluoro-2-nitroaniline is an amide that is a l1210 murine carcinogen. It is also an analytical reagent for the detection of nitrogen atoms in amines and thione compounds. 4-Fluoro-2-nitroaniline has been shown to be effective against cervical cancer, but not cancerous cells, which may be due to its ability to inhibit fatty acid synthesis. The carbon disulphide reacts with the nitro group of 4-fluoro-2-nitroaniline, resulting in the formation of a thione compound.

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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.

3-Formyl-6-nitrochromone is a type of sensor molecule that can be used in the detection of metal ions. It is an aromatic compound that has been shown to reversibly react with copper and other metal ions, which leads to a change in its fluorescence. 3-Formyl-6-nitrochromone reacts with the copper ion by donating an electron and forming a copper complex. This reaction is reversible, so it can be used as a sensor for copper ions. The sensor has been shown to have good spectral properties and chemosensors have been developed using this molecule.

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2-Fluoroethyl-Nitrosourea (2FEN) is a nitrosourea that has been used in the treatment of mammary carcinomas. It acts by inhibiting DNA synthesis and thus causing the death of cancer cells. 2FEN inhibits methylnitrosourea (MNU) induced mutagenicity in Chinese hamster cells, as well as MNU induced chromosome aberrations and micronuclei in f344 rats. The mechanism of this drug is not yet known. It has been shown to inhibit the reaction between MNU and DNA, leading to a decrease in the amount of adducts formed and thus a decrease in mutagenicity.

3-Amino-2-nitrotoluene (3ANNT) is an organic compound with the chemical formula C6H5N3O2. 3ANNT is a useful tool for wastewater treatment because it can be used to measure nitrogen atoms in wastewater. It is also used as an analytical method to measure the concentration of amines, nitro compounds, and other diazonium salts. The magnetic resonance spectra of 3ANNT show two hydroxyl groups and two nitro groups. The acute toxicities of 3ANNT are low, but the long-term effects are unknown.

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.

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

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Applications 1-Nitro-2-[(1E)-2-nitroethenyl]-4-(phenylmethoxy)-benzene is an intermediate used in the synthesis of 5-Hydroxyindole-3-acetic acid (H953605), which is an impurity of chlorpheniramine (C424300), an antihistaminic agent. References Josko, J., et al.: Annal. Acad. Med. Siles., 66, 13, (2012); Carson, R.P., et al.: Human. Molec. Genetics., 22, 140 (2013);

Nitrobenzene is a colorless liquid with an aromatic odor that is soluble in water and slightly soluble in alcohol. It is used as a chemical intermediate for the production of dyes and pharmaceuticals, as well as a solvent for paints and inks. Nitrobenzene's crystal structure consists of chains parallel to each other, which are bonded together by hydrogen bonds. The nitro group on one molecule can form a hydrogen bond with the amide group on another chain, stabilizing the molecule's structure. The benzene ring is planar and has four C-N bonds. This molecular arrangement gives nitrobenzene its stability and bonding properties.

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3-Nitrobenzylamine HCl is an intermediate in the synthesis of peptides. This compound is used to produce polypeptides and can be immobilized on a solid support for high yield production. 3-Nitrobenzylamine HCl can be covalently linked to a solid support by reacting with an activated carboxyl group and can undergo conformational changes upon irradiation with ultraviolet light or azobenzene derivatives. 3-Nitrobenzylamine HCl has been used in solid phase peptide synthesis, a technique that produces polypeptides at high yields. It is also used as a substrate for NMR techniques, which are useful for determining the nature of the molecule and its potentials.

2,2'-Dithio-bis(5-nitrophenyl) is a redox probe that can be used to study ATP-sensitive K+ channels. This probe has been shown to bind to the carboxy terminal of the channel and disulfide bond through its thiol group. The binding of 2,2'-dithio-bis(5-nitropyridine) to the activated liver cells causes an increase in the redox potential, which leads to an accumulation of electrons in these cells. These electrons are then transferred to pyridine nucleotides and phosphate ions, leading to an increase in ATP levels and activation of ATP-sensitive K+ channels.

N-(2-Methoxy-4-nitrophenyl)acetamide (DMNPA) is a potent anticancer agent that inhibits the synthesis of DNA. DMNPA is able to inhibit both the initiation and elongation steps in DNA synthesis. It crystallizes as needles or plates, with a melting point range of 191-194°C.

4-(4-Nitrophenylazo)resorcinol (NPAR) is a fluorescent dye that has been used to study the matrix effect of sodium salts. It is also used as a signal pathway marker for intracellular calcium ion levels, and to measure the pH of caproic acid. NPAR has been shown to be an acidic compound with a pK value of 4.5 in solid form and 5.5 in solution, based on its structural properties. NPAR has been shown to be an effective catalyst for hydrogen fluoride synthesis at elevated temperatures, and can be used as a fluorescent probe for brain functions. NPAR can also cause neuronal death at high concentrations, which may be due to its cationic surfactant properties.

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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.

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S-(-)-7-Desmethyl-8-nitro blebbistatin is a noncompetitive inhibitor of myosin light chain kinase that has been shown to be an efficient method for modelling cardiomyocytes. The effect of the drug on cardiac function and morphology in vitro can be visualized by using fluorescence microscopy. The drug also regulates adhesions between cells, which are important for organ function. S-(-)-7-Desmethyl-8-nitro blebbistatin is a reversible inhibitor that can be used to study the role of adenoviral morphologies on spontaneous cell culture.

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Applications 5-Nitro-1-benzofuran is a chemical reagent used in the synthesis of internal alkynes. Also used in the preparation of anti-oxidants quinolines. References Lu, L. et al.: Eur. J. Org. Chem., 2013, 1644 (2013); Kuzmin, V. et al.: Russ. Chem. Bull., 57, 2405 (2008);

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

5-Nitro-2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid (NTDPA) is an organic compound that is used as a precursor to other compounds. NTDPA is a stable complex with potassium ions and hydroxide solution. It reacts with water molecules in the presence of an electron donor such as n-dimethyl formamide to produce nitrite and carbon dioxide. NTDPA has been shown to be toxic to aquatic organisms at pH values greater than 8.5. This compound can cause symptoms such as severe headaches, vomiting, diarrhea, and skin rash in humans after prolonged exposure. It may also cause autoimmune diseases in animals and humans when exposed over a long period of time.

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4-Methyl-3-nitrobenzamide is a nitrile that can be synthesized by the reaction of potassium hydroxide and 3-nitrobenzamide. It has been shown to react with dichloroethane to form 4-methyl-3-nitrobenzoic acid. The optimum temperature for this reaction is 120°C, which leads to a high yield of 4-methyl-3-nitrobenzamide. This product is also available in an isotopic form at high purity.

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Diethyl-4-nitrobenzylphosphonate is an organic compound that has been shown to interact with the enzyme dihydropyrimidinase. This interaction leads to a change in the dihedral angle of the molecule, which can be measured using titration calorimetry. Diethyl-4-nitrobenzylphosphonate is also a pesticide and has been shown to cause Alzheimer's disease in mice. This compound is an aldehyde that reacts with decoupling agents such as acid or wittig reagents. Diethyl-4-nitrobenzylphosphonate is a molecule that contains four nitro groups, which are substituted at the 2nd, 3rd, 4th, and 5th positions on the benzene ring. It also contains one phosphorous group at the 1st position on the benzene ring. This ligand interacts with metal ions by donating electron density from its nitro

Applications 1,2-Dimethoxy-4,5-dinitrobenzene (cas# 3395-03-7) is a compound useful in organic 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

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1-(2-Fluoroethyl)-3-Cyclohexyl-1-Nitrosourea is a nitrogen mustard that inhibits the synthesis of DNA. It is an isomeric mixture of two enantiomers, one with a hydroxy group and the other without. The hydroxy group on the molecule is responsible for its cytotoxic activity. 1-(2-Fluoroethyl)-3-Cyclohexyl-1-Nitrosourea has been used as a diagnostic agent to detect guanine in nucleic acids and can be used as an antitumor agent in combination with other chemotherapeutic drugs. It has also been used as an adjuvant therapy to help treat solid tumors such as breast cancer. This chemical reacts with DNA by nucleophilic attack, where it attacks the 3' position of single stranded DNA, which causes transfer reactions that lead to double stranded breaks in the DNA strands. This drug also binds to RNA polymerase

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2-Methoxyethyl 2-(3-nitrobenzylidene)acetoacetate is a condensation product of acetoacetate and isopropyl alcohol. It is a white crystalline solid at room temperature. This compound has been shown to be an effective catalyst for the synthesis of nimodipine, which is used as an antihypertensive drug. The optimum reaction conditions are between -10°C and 30°C. The reaction can also be carried out in the presence of light, but it will not work in the dark. 2-Methoxyethyl 2-(3-nitrobenzylidene)acetoacetate is synthesized from 3-nitrobenzaldehyde and cyclization with ethanol or toluene. The result of this reaction is a white crystalline solid that melts at 190°C, with a boiling point of 256°C at 0.1 mm Hg pressure.

3-Nitrosalicylic acid is a chemical that is used as an inhibitor for corrosion. It can be used to prevent corrosion in wastewater systems, and it is also used as a protective coating for metals. 3-Nitrosalicylic acid has been shown to be effective against a variety of particle sizes, including fine particles at low concentrations. 3-Nitrosalicylic acid can be synthesized by reacting 5-nitrosalicylic acid with ammonia, hydrogen chloride, and zinc oxide in water. The reaction solution should be neutralized with sodium hydroxide and then hydrogenated using sodium dithionite or sodium sulfite. 3-Nitrosalicylic acid has been shown to inhibit the corrosion of metal surfaces and to function as an effective dose in the synthetic pathway for polymers. 3-Nitrosalicylic acid has high concentrations around pH 9.5, which can be reduced by electrochemical impedance spectroscopy (EIS).

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The Boc-D-phenylalanine 4-nitrophenyl ester is a chemical compound that can be used as a reagent to modify the conformation and structure of proteins. It has been shown to be an effective tool for optimizing, dampening, and analyzing protein conformations and structures. This chemical compound has also been used in chemists to study conformational changes in biomolecules. The Boc-D-phenylalanine 4-nitrophenyl ester is used in kinetic methods to study protein modifications and advances techniques to simulate the effects of this modification on the properties of proteins. This chemical compound is also used as a reagent for cyclic peptides with high values for lanthanide chelators.

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5-Phenylthio-2-nitroaniline (5PTNA) is an organic compound that is synthesized by the reaction of benzene and thiophenol in the presence of a catalyst. The catalyst used in this chemical reaction can be any metal or metal salt that has catalytic properties, such as nickel, iron, zinc, or copper. 5PTNA is primarily used as a precursor to other compounds through hydrogenation reduction. However, it can also be used as a target product for the synthesis of pharmaceutical drugs. The selectivity of this reaction can be optimized by using a catalyst with high catalytic activity and low reactivity towards 5PTNA. This increases the yield and selectivity of the desired product. 5PTNA is hazardous to humans because it can cause skin irritation from prolonged exposure to its liquid form. It may also cause eye irritation and damage to mucous membranes if it comes into contact with them.

N-Nitrosopyrrolidine is a chemical compound that is used as an organic solvent, pharmaceutical intermediate, and plasticizer. It reacts with DNA in vitro to form genotoxic activity, which may lead to cell death or mutagenesis. N-Nitrosopyrrolidine also has neurotrophic effects on primary cells and is an important precursor in the synthesis of polymers. The reactivity of N-nitrosopyrrolidine has been studied by kinetic energy spectroscopy and by measuring the intramolecular hydrogen transfer between nitroso groups. The mechanism of this reaction is not fully understood, but it appears to proceed through a dinucleotide phosphate intermediate with a high degree of kinetic energy.

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