Nitro

Please enquire for more information about 4-Bromo-3-nitrobenzenethiol including the price, delivery time and more detailed product information at the technical inquiry form on this page

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4-Methoxy-4'-nitrobiphenyl is a nitrated aromatic hydrocarbon that reacts with ultraviolet light to produce nitrobenzene. 4-Methoxy-4'-nitrobiphenyl is synthesised by the reaction of an aryldiazonium salt with nitric acid in the presence of an alcohol. The yields are dependent on the type of solvent used and the temperature. The product has been shown to have heterolytic properties, which can be analysed using ultraviolet spectroscopy.

Please enquire for more information about tert-Butyl(2,4-dibromo-6-nitrophenyl)diazene oxide including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Please enquire for more information about 1-[2-(5-Benzyloxy-2-Nitrophenyl)Vinyl]Pyrrolidine including the price, delivery time and more detailed product information at the technical inquiry form on this page

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

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Please enquire for more information about Ethyl 2,5-dimethyl-4-[(E)-2-nitrovinyl]-1H-pyrrole-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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

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.

4-Nitro-1,8-naphthalic anhydride is a fluorescent compound that has been shown to have endoplasmic and photochemical properties. It can be used as a donor in experiments that study the effects of hypoxic tumor cells on the stability of fluorophores. 4-Nitro-1,8-naphthalic anhydride can also be used to make amines, which are often used as cell culture media additives or reagents in biochemical reactions. The optical properties of 4-Nitro-1,8-naphthalic anhydride have been shown to depend on its functional groups. This compound fluoresces when it is bound to dna duplexes or nucleophilic compounds like amines.

Succinimidyl6-(N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino)hexanoate is a synthetic molecule that binds to phospholipid membranes and calcium. It has been shown to disrupt the fluidity of the membrane and induce changes in the distribution of lipids. The interaction between the compound and membranes may be due to hydrophobic interactions or an unlabeled carbohydrate moiety. Succinimidyl6-(N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino)hexanoate has been used as a model system for studying the interaction between viruses and host cells, specifically influenza virus binding to erythrocytes. This molecule has also been used as a fluorescent probe for immobilized lectins.

Please enquire for more information about Methyl 1-(2-nitrobenzyl)-pyrrole-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 4-Bromo-3-hydroxy-2-nitrobenzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 4-[(4-{[2-(4-Nitrophenyl)-2-oxoethoxy]carbonyl}phenyl)amino]-4-oxobutanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

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

Please enquire for more information about 5-Cholesten-3beta-ol3-p-nitrobenzoate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Please enquire for more information about (R)-(+)-2-(a-Methylbenzylamino)-5-nitropyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Bromo-4-fluoronitrobenzene is a molecule that has been shown to have an inhibition activity against the enzyme, tyrosinase. The reaction time for this reaction is dependent on the concentration of 3-bromo-4-fluoronitrobenzene and the temperature. The dipole moment of 3-bromo-4-fluoronitrobenzene has been calculated using computational methods. This molecular electrostatic potential is negative, which is indicative of its electrophilicity. 3-Bromo-4-fluoronitrobenzene has been shown to be reactive with other molecules and may be able to undergo chemical reactions with them.

Trans-4-Methoxy-beta-nitrostyrene is a chiral, catalytic compound that was synthesized from 4-methoxybenzaldehyde and nitrous acid. It has been shown to inhibit the growth of rat thoracic 5-hydroxytryptamine (5-HT)1A receptor neurons and prevent the activation of these receptors by serotonin in rats. Trans-4-Methoxy-beta-nitrostyrene may have therapeutic potential as an antidepressant or antiemetic drug. The mechanism of action is not fully understood, but it is thought that trans-4-Methoxy-beta-nitrostyrene binds to the active site on the 5HT1A receptor and blocks serotonin binding. Trans-4 Methoxy beta nitrostyrene has also been shown to inhibit folic acid synthesis in cancer cells, which may be due to its ability to inhibit methionine synthase through amines.

Please enquire for more information about (R)-3-Amino-3-(3-nitro-phenyl)-propionicacid including the price, delivery time and more detailed product information at the technical inquiry form on this page

1,3-Dichloro-5-nitrobenzene is a chemical intermediate used in the synthesis of carbamazepine. It is obtained by the desalting of 1,3-dichloro-5-nitrobenzene with water and methanol. The proton resonances are observed at 3.2 ppm and the dipole moment is 2.6 D. The chemical ionization mass spectrum shows a molecular ion peak at m/z (relative abundance) 144 and an isotopic pattern characteristic for C12H10Cl2N2O4+ (100%). The NMR spectrum shows three sets of peaks at δ 6.8, δ 7.4, and δ 8.6 that correspond to the two diastereomers of 1,3-dichloro-5-nitrobenzene: 1) CH3Cl+CH=CH2 + H+ → CH

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2-Nitro-5-fluorobenzoic acid, methyl ester is a compound that is used as a starting material for the synthesis of other compounds. It can be synthesized from methyl alcohol and nitrous acid. The resulting product is obtained by reacting with phosphorus pentoxide in a phosphotungstic acid solution at 0°C to produce a cyclic anhydride. This reaction is catalyzed by transfer catalyst, which promotes the formation of an anhydride ring. This product reacts with methyl alcohol and hydrogen peroxide to form a methyl ester, which can then be reacted with phosphotungstic acid to yield 2-nitro-5-fluorobenzoic acid, phosphonate.

Please enquire for more information about 4-(3-Nitro-4-piperazin-1-ylbenzoyl)morpholine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Glutaric acid-2-methylamino-5-nitromonoanilide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about HydrogenHydroxy[2-hydroxy-3-[(2-hydroxy-3-nitrobenzylidene)amino]-5-nitrobenzenesulfonato(3-)]chromate(1-)3-((2-ethylhexyl)oxy)-1-pr opanamine including the price, delivery time and more detailed product information at the technical inquiry form on this page

p-Nitropropionanilide is a nitro compound that is used as a bactericidal agent in the treatment of infections. It binds to extracellular proteins, such as those found on gram-negative bacteria, and forms an acetonitrile adduct that inhibits bacterial growth by competing with amino acids for transport across the cell membrane. p-Nitropropionanilide has been shown to be effective against Pseudomonas aeruginosa, even at concentrations below its bactericidal concentration. The drug is only active against gram-negative organisms and has neutral pH optima. p-Nitropropionanilide can be extracted from water using an organic solvent such as acetonitrile.

4-Hydroxy-3-nitrobenzoic acid ethyl ester is a small molecule that binds to DNA and RNA. It is cytotoxic, inhibiting cell growth in the presence of amides, nucleosides, or nucleotides. 4-Hydroxy-3-nitrobenzoic acid ethyl ester also inhibits the proliferation of cancer cells in culture. This drug has been shown to be effective against pancreatic cancer, ovarian cancer, and glioblastoma cells. The structure of this compound was elucidated by spectral analysis of its NMR and mass spectra data. It has yielded a 2780% increase in glioblastoma cell line growth rates when compared to control cells.

4'-Isopropyl-beta-methyl-beta-nitrostyrene is a versatile building block that can be used in the synthesis of complex compounds. It has been used as a reagent or speciality chemical in research and development, and as an intermediate for the synthesis of high quality, useful scaffolds. It is also a useful building block for the preparation of high quality, useful compounds.

1-(5-Chloro-2-nitrophenyl)ethanone (1) is a detectable and olefination sensitive precursor that is transformed to 2,4,6-trichlorophenylacetic acid (2) in a three-step transformation process. The transformation process starts with the conversion of 1 to phosphine oxide (3), followed by treatment with triethyl phosphite to give 3,5-dichloro-2-nitrobenzaldehyde (4). The final step involves reaction of 4 with an amine in the presence of a Lewis acid catalyst to give 2. END

Please enquire for more information about 2-{[2-(2-Methoxyphenoxy)ethyl]amino}-5-nitrobenzonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,2,4-Trimethyl-4-nitropentane is a liquid with a chromophore that exhibits a strong absorption band at 420 nm and a weak absorption at 600 nm. The molecule's electronic transitions are magnetic and it has vibrational properties. 2,2,4-Trimethyl-4-nitropentane can be used in the synthesis of nitroalkanes and as an additive to petroleum products.

Please enquire for more information about 4-(3-Nitro-pyridin-2-yl)-piperazine-1-carboxylic acid tert-butylester including the price, delivery time and more detailed product information at the technical inquiry form on this page

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5-Nitro-m-phenylenediamine is an organic compound that has the chemical formula CHNO. It is a white crystalline solid with a melting point of 158 °C. The compound is soluble in water and other polar solvents but insoluble in nonpolar solvents such as hexane. 5-Nitro-m-phenylenediamine can be prepared by nitration of m-phenylenediamine, which produces the desired product in about 30% yield and with impurities that must be removed by fractional crystallization. The compound is used as an intermediate for making dyes and pharmaceuticals. 5-Nitro-m-phenylenediamine is a precursor to various dyes, including acid yellow 23, acid red 51, and acid blue 9, which are all compounds used in textile printing. 5-Nitro-m-phenylenediamine can also be used to make pharmaceuticals such as

Please enquire for more information about 2-(3-Methyl-4-nitrophenoxy)propanohydrazide including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Nitro-1-naphthoicacid is an inhibitor of protein kinase C (PKC) that binds to the hydrophobic pocket in PKC. It has been shown to inhibit PKC, which plays a role in various cellular processes including cell proliferation, differentiation, and apoptosis. The inhibition of PKC leads to a decrease in the activity of cyclin D1 and cyclin E, which are important for the G2-M transition. 3-Nitro-1-naphthoicacid also inhibits kallikrein, an enzyme that is involved in the activation of bradykinin and is essential for blood coagulation. 3-Nitro-1-naphthoicacid has been found to be a potent fluorescent probe with fluorescence resonance energy transfer (FRET) properties.

Please enquire for more information about (3-(Trifluoromethoxy)phenyl)-2-nitropropene including the price, delivery time and more detailed product information at the technical inquiry form on this page

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(S)-N-(5-Nitro-2-pyridyl)phenylalaninol is the crystalline form of a yellow powder with an index of refraction of 1.6. It has a crystallographic space group P212121 and crystal structure that can be determined by x-ray analysis. The crystals are monoclinic, with a unit cell dimension of a = 7.858 Å, b = 10.36 Å, c = 6.04 Å, α = 89°, β = 90°, γ = 90° and Z = 4.

4-Acetamido-2',4'-dinitro-5'-methyldiphenyl sulphone is a high quality, versatile building block that is used as a reagent and complex intermediate. It can be used in the production of speciality chemicals, research chemicals and fine chemicals. 4-Acetamido-2',4'-dinitro-5'-methyldiphenyl sulphone is also a useful scaffold for the construction of new chemical compounds. This compound has been shown to be a reaction component in organic synthesis reactions.

1,8-Dinitronaphthalene is a chemical compound that belongs to the nitroarene family. It is soluble in organic solvents such as cyclohexane and benzene, but insoluble in water. 1,8-Dinitronaphthalene has been used as an adsorbent for heavy metal ions and other pollutants in water. The adsorption mechanism involves the formation of strong complexes between the pollutant and 1,8-dinitronaphthalene. The adsorption process is reversible and can be enhanced by adding phosphotungstic acid to the solution. 1,8-Dinitronaphthalene has also been used to study population growth of bacteria since it inhibits bacterial growth through a number of metabolic transformations that include hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase or conjugation with glucuronic acid.

Please enquire for more information about 4-(Cyclohexylthio)-3-nitrobenzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

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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.

3-Nitroisonicotinaldehyde is a kinase inhibitor that binds to the ATP binding site of receptor tyrosine kinases. It inhibits the activation of these receptors and prevents the phosphorylation of tyrosine residues on the receptor. 3-Nitroisonicotinaldehyde has been shown to inhibit VEGFR-2, ABCG2, and efflux in human cancer cells. This drug has been shown to inhibit tumor growth in mice by inhibiting angiogenesis, which is a process that involves the formation of new blood vessels from pre-existing ones. 3-Nitroisonicotinaldehyde also inhibits tumor growth by blocking the production of vascular endothelial growth factor (VEGF) from angiogenic cells.

3-Fluoro-2-nitropyridine is a fluorinated heterocycle that is activated by the presence of an electron withdrawing group, such as fluorine. This compound has been shown to inhibit pancreatic lipase and may be used to treat diabetes. 3-Fluoro-2-nitropyridine also reacts efficiently with alcohols in water at room temperature. The reaction product is a nitro compound that can be converted to an aliphatic amine by reaction with ammonia or amines. This conversion can take place through a method called synlett. The synlett method has been applied for the efficient preparation of various heterocycles and polyphosphoric acid advances have been made in this area of research.

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2-Methoxy-5-nitrobenzaldehyde is an amine that has been shown to be a potent anticancer agent. It is synthesized by the cross-coupling of 2,4,6-trimethoxyphenylacetonitrile with an amine. This compound has been shown to induce apoptosis in cancer cells by binding to DNA and inhibiting protein synthesis. 2-Methoxy-5-nitrobenzaldehyde also induces the M2 phenotype in macrophages and induces the production of fluorescent ethyl cinnamate from dihydrobenzofuran. The cross-coupling reaction is photolabile, making it difficult to study the mechanism of this compound's anticancer activity.

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2-Methyl-5-nitro-pyrimidine-4,6-diol is a bioactive molecule that has been shown to have antibacterial activity against Chromobacterium violaceum. This compound has also been shown to inhibit the growth of other bacteria such as Salmonella enterica, Escherichia coli, and Pseudomonas aeruginosa. It has a hydrophobic nature, which may be due to its ability to bind to the hydrophobic region of bacterial cell walls and membranes. The 2 methyl group on the pyrimidine ring may be important for binding because it strengthens the charges in this region. 2 METHYL 5 NITRO PYRIMIDINE 4 6 DIOL Stomatitis is an inflammation of the mouth lining and can occur in both humans and animals. Stomatitis can be caused by various factors including viral infections, radiation therapy, chemotherapy drugs, or trauma from oral surgery or

Please enquire for more information about Methyl [(4,6-dimethyl-3-nitropyridin-2-yl)oxy]acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,4-Dinitrophenylsulfenyl Chloride (2,4-DNPCl) is an allylating agent that reacts with nucleophilic groups to form covalent bonds. 2,4-DNPCl is a reactive compound that can react with various nucleophiles in basic solution. It has been found to be highly effective in the formation of dna duplexes and hydrogen bonding interactions with complementary strands. The chloride yields of 2,4-DNPCl are dependent on the reaction temperature and concentration of reactants. A high yield of chloride ions is observed when using methyl ketones as the substrate at low temperatures. The activation energies for the reaction mechanism of 2,4-DNPCl are determined to be 30 kcal/mol (98 kJ/mol). The carbonyl group is a key reactive functional group and participates in intermolecular hydrogen bonding and hydroxyl group hydrogen bond formation. 2,4-D

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2-Methoxy-5-nitrobenzonitrile is a chemical compound that belongs to the group of benzene, methyl ethers. It is an organic compound that has been shown to be a good nucleophile and is used in the synthesis of pyridine. 2-Methoxy-5-nitrobenzonitrile can exist as two stereoisomers, but only one of them (the erythro form) is stable at room temperature. The erythro form has a dipole moment, which allows it to react with nitrite ion or cyanide ion, forming an unstable nitroso species. This process can be used to synthesize 1-(2-methoxynitro)benzene from 2-methoxybenzonitrile and sodium nitrite.

Applications (E)-N-(2-((7-nitrobenzo[c][1,2,5]oxadiazol-4-yl)amino)ethyl)-4-oxo-4-phenylbut-2-enamide is a useful research chemical.