Nitro

<p>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.</p>

<p>O-(4-Nitrophenyl)hydroxylamine (OPH) is an enantioselective, catalytic, and thermal stable reagent for the synthesis of chiral methyl groups. OPH can be used as a nucleophile to convert electron-deficient alkenes into α-chloroalkenes. It also reacts with nitroarenes to give nitroalkenes in high yields. OPH has been shown to be effective in the asymmetric hydrolysis of esters and amides through its ability to oxidize the methyl group on the substrate. This reaction does not occur with other groups such as hydroxyl or hydrogen atoms.<br>Methyl groups are important for many biological molecules, including proteins and nucleic acids, which form the backbone of cells that make up living organisms. The OPH reaction is catalyzed by enzymes called methyltransferases, which transfer one atom of methyl from S-adenosylmethionine (SAM)</p>

<p>4-Nitrophthalic acid is a white crystalline solid that has an acid and basic character. It has been shown to be antigenic, with a specific antibody able to bind to the 4-nitro group. The structure of 4-Nitrophthalic acid was determined using X-ray crystallography and NMR spectroscopy. The molecular weight of 4-Nitrophthalic acid is 177.2 g/mol, with a melting point of 174 °C and a boiling point of 341 °C. It is soluble in water and organic solvents such as ethanol, acetone, chloroform, ethyl ether, benzene, hexane, dichloromethane and ethyl acetate.</p>

<p>1-(2',3'-Difluorophenyl)-2-nitroethene (1,2-DFNE) is a speciality chemical that is used as an intermediate for the synthesis of a wide variety of organic compounds. It has been found to be a useful scaffold for the synthesis of complex compounds and can also be used as a building block for the synthesis of fine chemicals, research chemicals, and versatile building blocks. 1,2-DFNE is soluble in many organic solvents and can be handled without special precautions. This reagent is a high quality compound with purity greater than 99%.</p>

<p>3-Amino-5-nitro-2,1-benzisothiazole is a diazonium salt that is used in wastewater treatment. It reacts with hydrogen peroxide to produce an unstable amine and a stable glycol ether. This process is known as the 3ABA reaction. The amine can be cleaved by water to produce ammonia and nitrous acid. Nitrous acid can react with organic matter in wastewater to form nitrate salts, which are soluble and easily removed from the wastewater stream. 3-Amino-5-nitro-2,1-benzisothiazole is also used in the manufacture of polyethylene terephthalate (PET) plastics. PET plastics are resistant to staining and have excellent color clarity.</p>

<p>2,7-Dinitrofluorene is a nitro compound that is used as an analytical reagent. It is used in the determination of redox potentials and is commonly used to measure the activity of nitroreductases. 2,7-Dinitrofluorene is also a genotoxic agent that causes DNA damage by producing reactive oxygen species (ROS), which react with DNA bases and cause strand breaks. Nitroreductase enzymes catalyze the reduction of nitro groups to amines, which are then converted to ammonia. This process produces ammonia, which reacts with other compounds in the body to form nitrosamines. Nitrosamines have been shown to be carcinogenic in animal models, and some of these compounds can be found in human tissues.</p>

<p>2,4-Dinitro-5-fluorotoluene is a fine chemical that can be used as a versatile building block in the synthesis of complex compounds. It is an intermediate in many reactions involving aliphatic nitro compounds and has been shown to be reactive with aromatic amines. This chemical has been used as a research chemical for the detection of proteins and nucleic acids and is also a good reagent for the synthesis of other chemicals. The compound reacts quickly with acid to produce a highly explosive gas which can be stabilized by reacting it with potassium nitrate or sodium bicarbonate.</p>

Please enquire for more information about 5,5-dimethyl-2-(((3-nitrophenyl)amino)methylene)cyclohexane-1,3-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>3-Nitrosalicylaldehyde is an oxidizing agent that reacts with DNA in vitro to form DNA adducts. 3-Nitrosalicylaldehyde also has antioxidative properties, which can be demonstrated by its ability to inhibit the oxidation of low density lipoprotein (LDL) in vivo. This compound has been shown to activate the metalloproteinase MT2 receptor, which is involved in the regulation of blood pressure and heart function. 3-Nitrosalicylaldehyde is metabolized by hydrolysis and reduction to form a neutral product, which has been shown to have antidiabetic effects on mice.</p>

<p>5-Bromo-2-cyano-3-nitropyridine is a medication that has been shown to be an effective inhibitor of the RET tyrosine kinase. It has been used in clinical studies to treat chronic kidney disease and has been shown to inhibit the growth of cancer cells. The molecular electrostatic potential (MEP) simulations have shown that 5-bromo-2-cyano-3-nitropyridine interacts with the reactive site of RET, inhibiting its function by binding to the nucleophilic substitutions. 5-Bromo-2-cyano-3-nitropyridine is synthesized from 2,5 dibromopyridine and 3 nitrobenzene at high yield. The molecule is chromatographically separated from impurities such as 4 bromo pyridine.</p>

<p>Please enquire for more information about 2-[(Ethylamino)methyl]-4-nitrophenol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Fluoro-2-nitrobenzonitrile is a synthetic compound that has been shown to inhibit the growth of tumor cells. It binds to nucleic acids and causes DNA damage, which leads to cell death. 5-Fluoro-2-nitrobenzonitrile inhibits the synthesis of proteins in cancer cells and also induces their apoptosis. The molecular modeling data indicates that this molecule has a hydrophobic pocket that can be used for targeting tumour cells. X-ray crystallography studies have confirmed that 5-fluoro-2-nitrobenzonitrile binds selectively to the minor groove of dna, suggesting its inhibitory potency against tumour cells.</p>

<p>Methyl 4-amino-3-nitrobenzoate is a synthetic compound that has been found to have a variety of uses. It has been used to prepare intramolecular hydrogen bonds in anilines, and it can be used as an intermediate to synthesize amides and anilines. This molecule also forms resonance structures with the nitro group, which allows for increased stability. The proton magnetic resonance spectra of Methyl 4-amino-3-nitrobenzoate show that the molecule has a high degree of symmetry, which is due to the presence of intramolecular hydrogen bonding.</p>

<p>1,8-Dihydroxy-4,5-dinitroanthraquinone (1,8DDNA) is a chemical inhibitor that inhibits the protease activity of ns3 protease. 1,8DDNA has been shown to inhibit the replication of wild-type virus in cell culture. This molecule also inhibits methyl transferase and structural analysis. The second-order rate constant for this compound was found to be 0.64 M-1s-1 at pH 7.5 in the presence of 10 mM NaCl and 5 mM Tris buffer at pH 8.0. 1,8DDNA's solubility data indicates that it is soluble in water with a solubility limit of 9 g/L at 25°C; however, its solubility decreases as the temperature increases.</p>

<p>Methyl 3-hydroxy-4-nitrobenzoate is a surfactant that has been shown to interact with toxins in the environment, such as polycyclic aromatic hydrocarbons. Methyl 3-hydroxy-4-nitrobenzoate interacts with these toxins by forming heterodimers and stabilizing them in solution. This interaction is achieved through hydrophobic interactions between the carboxylate group of methyl 3-hydroxy-4-nitrobenzoate and the other molecule's hydrophobic regions. The thermodynamic parameters for this interaction are determined by titration calorimetry.</p>

<p>1-(4-Nitrophenyl)glycerol has been shown to inhibit the growth of Gram-positive bacteria, including Streptococcus faecalis, and Gram-negative bacteria, including Pseudomonas aeruginosa. It is also used as a sample preparation for antimicrobial resistance testing.</p>

<p>3-Fluoro-2-nitrobenzoic acid ethyl ester is a fine chemical that is useful as a versatile building block in the synthesis of complex compounds. It can be used as an intermediate in the preparation of research chemicals and has been shown to react with amines to form nitrosoamines, which are useful reaction components. 3-Fluoro-2-nitrobenzoic acid ethyl ester has CAS number 163077-89-2 and is available at high quality.</p>

<p>3-Bromo-2-hydroxy-5-nitrobenzaldehyde is a hydroxy group with a formyl group, an imine and an isomeric structure. It can be used as a fluorescence probe in biological studies. The compound has been shown to have antioxidant activity, which may be due to its ability to donate hydrogen bonds or its ability to act as a phenylhydrazone. 3-Bromo-2-hydroxy-5-nitrobenzaldehyde also has the ability to react with ammonium nitrate and produce nitrogen gas (NH3) when heated. This reaction is exothermic and produces an orange color.</p>

<p>1-(2-Hydroxyphenyl)-2-nitroethene is an organocatalytic biomolecule that has been synthesized in an asymmetric fashion. The synthesis of the molecule relies on a squaramide and the use of intramolecular hydrogen transfer reactions to create a nitro group. The molecule was used to generate antiestrogenic activity in MDA-MB-231 breast cancer cells and MCF-7 breast cancer cells by inhibiting estrogen receptor alpha (ERα) transcriptional activity. This molecule has also been shown to be bifunctional, as it inhibits both protein kinase C (PKC) and mitogen-activated protein kinase (MAPK) signaling pathways when applied to these cell lines. X-ray crystal structures of the molecule have been obtained with orientations that exhibit different degrees of hydrophobicity, which may be due to interactions with water molecules.</p>

<p>p-Nitrobenzyl 6-(1'-hydroxyethyl)-azabicyclo(3.2.0)heptane-3,7-dione-2-carboxylate is a drug substance that is used in the manufacture of carbapenem antibiotics. It can be detected by a chloride ion chromatographic method, and the detection limit is 0.5 mg/L in the presence of zinc powder as a modifier. This material is used to prepare carbapenems using an analytical method that includes reaction monitoring by optical rotation, diastereomer chromatography, and transfer.</p>