Nitro

<p>L-Leucine 4-nitrophenyl ester hydrochloride is a reaction component, reagent, and useful scaffold that is used in the synthesis of complex compounds. It is a versatile building block and useful intermediate that can be used to synthesize fine chemicals such as pharmaceuticals, agrochemicals, or dyes. L-Leucine 4-nitrophenyl ester hydrochloride has CAS number 75691-76-8.</p>

<p>2-Nitro-4-(trifluoromethyl)benzaldehyde is an immunosuppressive agent that binds to the active site of the enzyme nitric oxide synthase, inhibiting its activity. This drug has been shown to be active against human immunocompromised patients and those with a history of melamine exposure. It also inhibits the production of nitric oxide, which is associated with inflammation. 2-Nitro-4-(trifluoromethyl)benzaldehyde has been shown to bind to vinylic positions on proteins, leading to immunosuppression.</p>

<p>2-Nitrophenylacetone is a polycyclic compound with an alkyl group, phenyl group, and a diterpenoid substituent. It is acylated with an acetate group on the 2-nitrophenyl group. The skeleton of this molecule contains a ketone (C=O) framework. The hydrogen atom in the molecule constitutes its chemistry. This molecule has been expressed in E. coli and purified to homogeneity. It constitutes the first example of a ketone containing framework for which biomolecular chemistry has been studied.</p>

<p>2-Hydroxy-5-nitroacetophenone is a synthetic molecule that has two functional groups. It is synthesized by reacting morpholine with malonic acid. 2-Hydroxy-5-nitroacetophenone is an electron donor, which means it can accept electrons from other molecules. This compound can be used as a diagnostic tool for cancer cells because it reacts with oxygen to form polyhedra, which are indicative of cancer senescence. In addition, this compound can be used to measure the concentration of plasma mass spectrometers by using electron spin resonance (ESR) and magnetic resonance imaging (MRI). The unpaired electrons on the nitro group of the molecule react with oxygen in the air to form polyhedra and give off characteristic signals in ESR and MRI. These signals are proportional to the concentration of unpaired electrons and therefore provide a quantitative measurement of 2-hydroxy-5 nitroacetophenone in solution.</p>

<p>Usnic acid is a dietary supplement that has been shown to have beneficial effects on the liver, including hepatoprotective and anti-inflammatory properties. Usnic acid prevents mitochondrial membrane potential from decreasing, leading to an increase in adenine nucleotide content and improved mitochondrial function. Usnic acid also reverses the inhibition of monoamine neurotransmitters caused by chemical ionization and pharmacologic agents such as acetaminophen. Usnic acid also has been shown to be effective against hepatitis A virus (HAV) infection in CD-1 mice.</p>

<p>1,5-Dinitronaphthalene is a test compound that has been used in the analytical method to determine the presence of basophilic leukemia cells. This reaction mechanism involves hydrogen bonding interactions with naphthalene, which is a test sample. The results are then read by chromatographic science and solubility data are collected. The 1,5-dinitronaphthalene can be used as a test compound for steric interactions with other compounds. It can also be used to measure the solubility of other compounds in different solvents.</p>

<p>3'-Fluoro-4'-methoxy-beta-methyl-beta-nitrostyrene is a reactive building block that can be used in the synthesis of many different compounds. It is a fine chemical and a reagent which is useful in organic chemistry. 3'-Fluoro-4'-methoxy-beta-methyl-beta-nitrostyrene is used as a reaction component for the synthesis of many different compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. It has CAS number 1023717-11-4 and can be used as an intermediate compound or building block for the production of complex compounds.</p>

<p>4-Chloro-7-nitrobenzofurazan is a fluorescent derivative that binds to the α subunit of DNA polymerase. It can be used as an analytical method for the detection of DNA polymerase inhibitors. 4-Chloro-7-nitrobenzofurazan has also been shown to inhibit cell nuclei and human serum, as well as binding to reactive sites on human cells. This compound can be used in control analysis for laboratory experiments related to protein synthesis and cell death.</p>

<p>2,6-Dimethoxy-3-nitrobenzoic acid is an aromatic compound that has been shown to have a molecular weight of 136.2 g/mol. It is extracted from the leaves of "Nepeta cataria" and can be found in many other plants as well. This compound has been shown to inhibit bacterial growth in vitro by inhibiting protein synthesis. The mode of action for this compound is not yet known, but it may be due to its ability to form hydrogen bonds with the ribosomes and inhibit nucleotide binding sites on the ribosome surface.</p>

<p>Please enquire for more information about Pigment YellOw 5;2-[(2-NitrOphenyl)azO]-3-OxO-N-phenylbutanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 1-(4-Cyanophenyl)-2-nitropropene including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Nitro-5-(trifluoromethyl)benzene-1,2-diamine is a chemical compound that can be used as a reaction component or reagent in research. It is a useful scaffold and building block for complex compounds. 3-Nitro-5-(trifluoromethyl)benzene-1,2-diamine has CAS No. 2078-01-5 and is classified as a speciality chemical. This chemical is versatile because it has many uses in both organic chemistry and biology, including use as an intermediate or building block for more complex compounds.</p>

<p>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.</p>

<p>4-Amino-3-nitrophenol is a reactive aminophenol that can be synthesized from hydrogen sulfate and diethyl ester. It is used in the synthesis of amines and other chemicals, as well as in analytical methods for determining the concentration of nitrates, nitrites, and aminophenols. 4-Amino-3-nitrophenol has been shown to have photocatalytic activity.</p>

<p>3-Amino-3'-nitrobiphenyl hydrochloride is a versatile intermediate that can be used in the synthesis of complex compounds. It is a white crystalline solid with a melting point of 178 °C. This product is soluble in water, methanol, ethanol, acetone and chloroform. 3-Amino-3'-nitrobiphenyl hydrochloride has many applications including research chemicals and speciality chemicals.</p>

<p>4-Bromo-2-nitrotoluene is a solvent with an orange color. It has been shown to have antimycobacterial activity and insecticidal activities, as well as being a potent anticancer agent. This compound is often used in the synthesis of β-carboline alkaloids and can be debrominated to form bromobenzene, which is used in the synthesis of phenolic compounds. 4-Bromo-2-nitrotoluene also inhibits the growth of human breast cancer cells.</p>

<p>4-Nitrobenzyl (4R,5R,6S)-3-[(diphenylphosphono)oxy]-6-[(R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylat e is a synthetic compound that is used as an alkalizer and impurity scavenger in the manufacture of pesticides and other organic chemicals. It has been shown to be a stereoselective herbicide with acetonitrile as its primary degradation product. The compound has also been found to be a potent inhibitor of the enzyme carbapenemase, which may lead to increased resistance to antibiotics such as monosodium salt of ertapenem.</p>

<p>2-Nitrobenzaldehyde is a nitro compound that reacts with the intramolecular hydrogen of an alkene to form a nitroalkane. It is used as an antimicrobial agent, in which it inhibits the growth of bacteria by reacting with the intermolecular hydrogen bonding in the bacterial cell membrane. In addition, 2-Nitrobenzaldehyde has been shown to inhibit fatty acid synthesis and transfer reactions. The optimum concentration for this chemical is 0.01% to 0.1%. This chemical is soluble in both water and organic solvents, such as methanol and ethanol.</p>

<p>Methyl 6-nitroveratrate is an organic compound that is used as a reagent in organic synthesis. It is synthesized by the conversion of methyl 3-nitrobenzoate, an ester of benzoic acid, to methyl 6-nitrobenzoate with nitrous acid. Methyl 6-nitroveratrate has been shown to be metabolically stable and can be used in biochemical studies. Methyl 6-nitroveratrate also has protonation properties that are complementary to acetylcholine, which may account for its use as a comparator in pharmacological experiments. The molecule was postulated to have a role in synopses, but this has not been proven.</p>

<p>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.</p>

<p>4-Bromo-6-nitro-m-xylene is a fine chemical that belongs to the group of reagents and speciality chemicals. It is a versatile building block that can be used as a reaction component or intermediate in the synthesis of complex compounds. 4-Bromo-6-nitro-m-xylene has been shown to react with nucleophiles, such as amines, alcohols, and thiols, to form nitrosamines. This chemical has been used as a research tool for studying the mechanism of action for various drugs. The compound is also useful as a scaffold for other complex compounds.</p>

<p>3-(4-Nitrophenyl)propanoic acid is an inhibitor of aminopeptidases. Amino acid catabolism, in particular the cleavage of peptides by proteolytic enzymes, is a central process in cellular metabolism. Amino acid catabolism is regulated by a number of different enzymes, including aminopeptidases. 3-(4-Nitrophenyl)propanoic acid inhibits the activity of these enzymes and thereby prevents the degradation of amino acids. This product has been shown to inhibit aminopeptidase A with an IC50 value of about 0.5 mM and aminopeptidase B with an IC50 value of about 1 mM. 3-(4-Nitrophenyl)propanoic acid also has anti-inflammatory properties that may be due to its inhibition of prostaglandin synthesis.</p>

<p>2,6-Dinitrobenzene-1,4-dimethanol is a developer that has been shown to have a sensitivity of 0.5 mg/ml and a molecular weight of 235.3 g/mol. It is also an amplified developer that has been shown to reduce the weight of polymers by up to 20%. This molecule can be used for the production of polymers with functional moieties and monomers with chemically reactive groups. 2,6-Dinitrobenzene-1,4-dimethanol is soluble in organic solvents and can be used as a monomer in polymerization reactions.</p>

<p>2-Nitro-4-tert-butylphenol is a phenolic antioxidant that has been used as a substitute for 2,6-di-tert-butylphenol (BHT) in cellulose triacetate. It also has been used in the production of 16-membered macrolides and macrocyclization reactions. 2NBP has been shown to be a potent inhibitor of ionophore transport across membranes, with the ability to inhibit membrane protein function and affect macrocyclization. It is also able to form mesoporous materials with diameters in the range of 10 nm to 100 nm. Nitroarenes are good candidates for molecular size control because they can be easily synthesized by addition reactions, which makes them ideal for use in organic chemistry.</p>

<p>4'-Hydroxy-3'-nitroacetophenone is a synthetic compound that has been used as an xanthine oxidase inhibitor. It has been shown to reversibly inhibit xanthine oxidase and prevent the accumulation of toxic metabolites that are produced by this enzyme. 4'-Hydroxy-3'-nitroacetophenone also inhibits the activities of other enzymes, such as covalent adducts with protein molecules and transfer reactions. The molecular modeling study of this compound showed that it binds to the active site of xanthine oxidase, forming a covalent adduct between the reactive oxygen species (ROS) and the phenolic OH group on the inhibitor molecule. 4'-Hydroxy-3'-nitroacetophenone was found to be safe in clinical studies, with reversible covalent binding and no inhibition of protein synthesis or cell growth at therapeutic concentrations.</p>

<p>N-Nitrosoethylmethylamine (NMMA) is a nitrosamine that can be found in water vapor. It has been shown to cause cell lysis and has been detected by LC-MS/MS using an in vitro assay. NMMA is readily soluble in water, making it a suitable candidate for wastewater treatment. This molecule is not cytotoxic or mutagenic but does have carcinogenic potential. NMMA also exhibits matrix effects that are dependent on the type of solvent used for extraction, as well as fluorescence spectrometry results. It was found to be a potent inducer of enzymes such as beta-lactamase, DNA gyrase, and topoisomerase IV, which may be useful for studying gene expression. Dispersive solid phase extraction can be used to extract NMMA from water sources such as soil and drinking water samples.</p>

<p>2-Iodo-4-nitrotoluene is an analytical reagent that is used in chromatographic methods for the separation of copper complexes. It reacts with copper to form a copper complex, which can be detected by UV spectroscopy. 2-Iodo-4-nitrotoluene has been used as a reagent for the detection of antimalarial activity and also as a reagent for determining the presence of amines. The technique involves reacting 2-iodo-4-nitrotoluene with ammonia or an amine, forming a nitrosoamine that can be detected by nmr spectra. This chemical is reusable and yields high purity products, making it an ideal choice for techniques involving solvents.</p>

<p>N-Nitroso-N-phenylhydroxylamine aluminium (NNPA) is a nitrated organic compound that belongs to the thioxanthone family. It is a colorless, oily liquid that has a strong odor of hydrochloric acid. NNPA is used in the production of polyester resins and coatings, as well as in the manufacture of methacrylate polymers. The reaction system for this compound consists of aluminum chloride and calcium carbonate. This substance can be prepared by reacting trimethylolpropane with methacrylates and magnesium in an organic solvent such as isopropyl alcohol or acetone. NNPA can also be synthesized by reacting zinc powder with ammonium bicarbonate, followed by carbamoylation with an organic amine such as isopropylcarbamate.</p>

<p>2-(4-Chloro-3-nitrobenzoyl)benzoic acid is a high quality, reagent, and complex compound that is useful as an intermediate. It has the CAS number of 85-54-1 and is classified as a fine chemical. This compound can be used as a building block for speciality chemicals or research chemicals. It is also a versatile building block for reactions and has many applications in synthetic chemistry.</p>

<p>3-Methyl-4-nitroanisole is a chemical compound used in the preparation of other compounds. It is obtained by reacting nitromethane with anisole in the presence of hydrochloric acid and a catalyst such as zinc chloride or copper chloride. It can be used to make melatonin, which is a hormone that regulates sleep cycles and seasonal changes in animals. 3-Methyl-4-nitroanisole can also be used to prepare nitrophenol, which is a precursor in the production of nylon. The luminescent properties of 3-methyl-4-nitroanisole are useful for analytical techniques such as UV spectroscopy, which can detect concentrations of this chemical at less than 1 ppm.</p>

<p>1-(2,5-Dimethoxyphenyl)-2-nitroethanol is a chiral, asymmetric catalyst that has been shown to be effective in the enantioselective reduction of ketones. This process is important because it allows for the synthesis of chiral amino alcohols, which are then used in a variety of chemical reactions. The reaction can also be carried out with methyl amine as an amine source. 1-(2,5-Dimethoxyphenyl)-2-nitroethanol is an example of a catalyst that participates in catalysis through the lone pair on oxygen and nitrogen atoms.</p>

<p>4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) is a metabolite of nicotine that has been shown to be carcinogenic in vivo. It binds to DNA, forming adducts with guanine, and can cause mutations and chromosomal aberrations. 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol is excreted in urine as a glucuronide conjugate. Its potential use as a biomarker for tobacco smoking has been demonstrated by the observation of increased levels following exposure to cigarette smoke. The urinary concentration of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol has been correlated with the risk for lung cancer in humans, and it may be useful as an analytical method for determining tobacco consumption.</p>

<p>2-Methyl-6-nitrophenol (2MP) is a nitro compound that has been shown to have an inhibitory effect on the oxidation of sodium nitrate by sodium chloride. It also inhibits the photooxidation of biomimetic systems. 2MP is a chemical ionization reagent that can be used as a molecular descriptor in environmental chemistry studies. The regioselectivity of 2MP was studied using gas chromatography and mass spectrometry. The molecular descriptors were determined using electron ionization and chemical ionization, which were found to be similar.</p>

<p>1-(4-Bromophenyl)-2-nitropropene is a synthetic molecule that undergoes an efficient cycloaddition reaction with aldehydes. This reaction is used to synthesize 1,3-dienes and alpha,beta-unsaturated carbonyl compounds. When the substrate is an aldehyde, the final product is a 1,3-diene. When the substrate is an alpha,beta-unsaturated carbonyl compound, the final product is an alpha,beta-unsaturated ketone.</p>

<p>2-Acetamido-5-nitrobenzoic acid methyl ester is an organic molecule that has the chemical formula C7H6N2O4. This compound belongs to a class of compounds called diazo compounds, which are characterized by a nitrogen atom with two bonds to carbon atoms and one bond to oxygen. 2-Acetamido-5-nitrobenzoic acid methyl ester is soluble in water and methanol. It has been shown to be chiral and exhibits optical activity. The experimental results show that the compound can exist in two different forms or conformations, which are distinguished by their x-ray diffraction patterns. These conformers have been identified as (1) the protonated form and (2) the torsion form. The protonated conformer has a molecular structure that contains a benzene ring with a hydrogen atom attached to it, while the torsion conformer does not contain this hydrogen atom</p>

<p>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.</p>

<p>4-Chloro-3,5-dinitrobenzoic acid is a redox potential chemical that has been shown to be reactive in the presence of nucleophiles. The toxicological studies on this chemical have focused on its hemolytic activity and conformational properties. 4-Chloro-3,5-dinitrobenzoic acid is a molecule with neutral ph and can react with lysine residues in proteins, which may lead to the release of caproic acid and nitrite ions. This chemical also has protease activity and can undergo transfer reactions with other molecules.</p>

<p>Methyl 2-methyl-3-nitrobenzoate is a synthetic drug that has potent antitumor activity and inhibits tumor growth in a variety of animal models. It acts by inhibiting protein synthesis and inducing apoptosis, as well as by inhibiting the production of TNF-α. Methyl 2-methyl-3-nitrobenzoate is an alkylating agent that reacts with DNA, RNA, and other cell components to form crosslinks between them. This prevents the cells from dividing or repairing themselves. The inhibition of protein synthesis may be due to methyl 2-methyl-3-nitrobenzoate's ability to react with amide groups on proteins.</p>

<p>(S)-(+)-N-(3,5-Dinitrobenzoyl)-alpha-phenylglycine is a chiral compound that is made up of two enantiomers. It has been shown to be a potent anthelmintic drug, but it is not currently used clinically due to its high toxicity. This compound destroys the parasite's gut lining by reacting with sulfoxide and capillaries in the intestine. The sulfoxide reacts with the pyrrole to form a sulfoxonium ion, which reacts with amino acid residues in the parasite's cell membrane to form a covalent bond. This reaction disrupts the integrity of the parasite's cell membrane and leads to cell death.</p>

<p>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.</p>

<p>2-Methoxy-5-nitropyridine is an experimental model for the study of nucleophilic substitution reactions. It has been shown to catalyze a variety of nucleophilic substitutions, such as the reaction between dimethylformamide and methoxide. The uptake of 2-methoxy-5-nitropyridine in human cells has been studied using the mitochondrial cytochrome P450 (mt2) receptors, where it has been found that this compound binds to mt2 receptors with high affinity. The optical properties of 2-methoxy-5-nitropyridine have been determined by spectroscopic analysis and found to be similar to those of nitro compounds. Toxicity studies have also demonstrated that 2-methoxy-5-nitropyridine can cause liver damage at high doses, but there is no evidence that it causes cancer or causes reproductive toxicity.</p>

<p>3-Nitrophenylmethylcarbinol (3NP) is a chiral molecule that is used as a versatile catalyst in organic synthesis. It has been shown to be an efficient and reusable nucleophile, which can be used for the hydrothiolation of enones. 3NP also has been shown to have high activity in asymmetric oxidation reactions, such as the conversion of alcohols to ketones or aldehydes. 3NP has been shown to be an excellent reagent for the conversion of carbinols into alkenes, due to its high oxidation potential.</p>

<p>2-Ethoxy-5-nitropyridine is a potassium salt of 2-ethoxy-5-nitropyridine. It has been used as a reagent in the synthesis of sulfonates, pyridines, and phenols. The nitrogen atom in this molecule can be oxidized to nitro group. This compound also reacts with anilines to form 2-chloro-5-nitropyridine and 2-hydroxy-5-nitropyridine. In addition, it can react with halogen to form substituted anilines or chloropyridines. 2-Ethoxy-5-nitropyridine is a nucleophile that can be used for the preparation of nucleophiles for biomolecular chemistry studies.</p>

<p>5-Methyl-2-nitrobenzoic acid is a nitro compound that has been shown to have potent cytotoxicity in vivo. 5-Methyl-2-nitrobenzoic acid inhibits the proliferation of cervical cancer cells in vitro, and induces apoptosis. The functional groups present on this molecule are nitro and methyl. The linear model used to describe the structure of 5-methyl-2-nitrobenzoic acid is an electron withdrawing group, which is why it has such potent cytotoxic effects. It also shows optical properties such as vibrational spectroscopy, which can be used to identify this molecule</p>

<p>4-Bromo-2-fluoro-1-nitrobenzene is a molecule that has anticancer activity. It inhibits cancer cells, but does not affect normal cells. The mechanism of action of 4-bromo-2-fluoro-1-nitrobenzene is not yet known. However, it may be due to its ability to react with the prenyl group in the cell membrane, which is important for cell growth and division. The human liver metabolizes 4-bromo-2-fluoro-1-nitrobenzene by kinetic and thermodynamic properties. This drug also has pharmacokinetic properties and can be detected in the bloodstream, urine, and feces for up to two weeks after administration. Fatty acid metabolism can cause drug reactions when taken with 4bromo2furo1nitrobenzene. Protein–protein interactions can also lead to side effects when taking this drug, such as enzyme inhibition</p>

<p>4-Nitro-L-phenylalanine methyl ester hydrochloride is a 4-nitrophenyl derivative of L-phenylalanine. It is a useful building block, reagent, or scaffold in organic synthesis. This compound finds use as a precursor to other derivatives and it has been used in the preparation of complex compounds. 4-Nitro-L-phenylalanine methyl ester hydrochloride is also used as a reaction component for the synthesis of different organic compounds and as a useful intermediate.</p>

<p>L-alanine 4-nitroanilide hydrochloride (H-Ala-pNAHCl) functions as a substrate for L-alanine aminopeptidase, an enzyme found in bacterial cell walls that catalyzes the cleavage of L-alanine from peptides. Notably, significant activity of L-alanine aminopeptidase is specific to gram-negative microbes. Thus, the utilization of H-Ala-pNAHCl can provide evidence for distinguishing between gram-positive and gram-negative organisms. When acted upon by L-alanine aminopeptide, it undergoes cleavage into L-alanine and 4-nitroanine, with the latter compound causing bacterial suspensions to exhibit a yellow coloration.</p>

<p>2,6-Dichloro-1,5-dinitronaphthalene is an organic compound that is used as a reagent for the synthesis of other compounds. It can also be used in research for the synthesis of 2,6-dichloro-1,5-dinitronaphthalene derivatives. The CAS number for this compound is 320600-07-5. This compound is a versatile building block and has many uses as a fine chemical.</p>

<p>1-(3-Hydroxyphenyl)-2-nitroethene is an organocatalytic chiral catalyst that has been shown to catalyze the asymmetric synthesis of a variety of organic compounds. The synthesis proceeds in two sequential steps: first, the enantioselective addition of nitroethane to a chiral thiourea followed by lactonization with quinine. This is an example of an asymmetric catalytic process.</p>

<p>2-Bromo-4-nitrotoluene (2BNT) is a mononitro substituted aromatic compound and a potent inhibitor of protein synthesis. It has been shown to have antimalarial activity, but it is not known to what extent the inhibition of protein synthesis contributes to its anti-malarial activity. 2-Bromo-4-nitrotoluene is also used in the preparation of imatinib, an anticancer drug that inhibits the growth of certain types of cancer cells. It can also be used as an inhibitor in vibrational spectroscopy.</p>

<p>1,3-Dinitroadamantane is a reactive compound that is used in the synthesis of 1-nitropropane. It is also used as a catalyst for the conversion of phosphoribosyl pyrophosphate to adenosine monophosphate. 1,3-Dinitroadamantane can be hydrolyzed by carbon tetrachloride and acyclovir to form guanosine and leishmania. This compound has also been shown to cause regression of visceral leishmaniasis in mice. The mechanism of action for this compound is not yet known but it may involve the conversion of purines to pyrimidines or inhibition of DNA synthesis.</p>

<p>2-Chloro-3-nitrobenzonitrile is a high quality, reagent, and complex compound that is useful as an intermediate for the synthesis of fine chemicals. It has CAS No. 34662-24-3 and can be obtained from chemical suppliers worldwide. The compound is also useful as a building block for the synthesis of pharmaceuticals and other speciality chemicals. 2-Chloro-3-nitrobenzonitrile is a versatile building block that can be used in organic reactions to produce research chemicals such as derivatives of indole or phenol compounds.</p>

<p>Trans-2,5-dimethoxy-4'-nitrostilbene is a molecule that belongs to the class of polycyclic aromatic compounds. It is used as a versatile building block in organic synthesis, and is also an intermediate for the production of other compounds. Trans-2,5-dimethoxy-4'-nitrostilbene has been shown to be effective in the preparation of various pharmaceuticals such as diazepam and chloramphenicol. It is also used in research chemicals and speciality chemicals. The structure of trans-2,5-dimethoxy-4'-nitrostilbene can be described as a bicyclic compound with two phenyl rings joined by an oxygen bridge. Trans-2,5-dimethoxy-4'-nitrostilbene has CAS No. 552938 4 and molecular weight of 268.81 g/mol.</p>

<p>3-Hydroxy-4-methoxy-2-nitrobenzaldehyde is a ternary complex that has been adsorbed onto the surface of an ion exchange resin. The adsorption process occurs through the formation of hydrogen bonds between the hydroxyl groups on the resin and the hydroxyl groups on the molecule. This complex is also soluble in chloroform, which may be due to its ability to form hydrogen bonds with itself and other molecules. The 3-hydroxy group on this molecule has been shown to react reductively with nitrophenol, forming a nitroso derivative. 3-Hydroxy-4-methoxy-2-nitrobenzaldehyde has been used as a template for the microbiological assay of azides and quinones.</p>

<p>4-IsoPropylphenylnitroethene is a fine chemical that is used as a versatile building block in the synthesis of complex compounds. 4-IsoPropylphenylnitroethene is an intermediate that can be used to synthesize other chemicals, such as research chemicals and reaction components. It can also be used as a reagent or speciality chemical. This compound has high quality, making it useful for research purposes.</p>

<p>7-Nitroindole-2-carboxylic acid is a molecule that has been shown to inhibit the activity of cytidine deaminase, an enzyme involved in the synthesis of DNA. This drug also inhibits the replication of dna and can be used for the treatment of cancer. 7-Nitroindole-2-carboxylic acid binds to basic proteins and has a helical structure. The affinity constants for this compound have not been reported, but it is thought that hydrogen bonding interactions are involved in its binding.</p>

<p>4'-Benzyloxy-3'-nitroacetophenone is a nitro-substituted aromatic compound that has been studied as an inhibitor of xanthine oxidase. It is also known to inhibit cytochrome P450 and nitric oxide synthase. The molecular modeling study showed that 4'-benzyloxy-3'-nitroacetophenone binds to the active site of xanthine oxidase and blocks the binding site for xanthine, which stops the conversion of xanthine to uric acid. This inhibition leads to a decrease in urate production, which can help prevent gout attacks.</p>

<p>2-Chloro-N-(2-nitrophenyl)acetamide is an antimicrobial agent that is a ligand for thionyl chloride. It has efficient methods of production and can be used as a bioactive molecule in the synthesis of aminosulfonyl chlorides, amide chlorides, or transfer chlorides. This compound reacts with gram-negative bacteria by hydrolyzing chloride ions to produce nitrosyl chloride and releasing hydrogen gas. The reaction time and functional groups are determined by the parameters chosen for the reaction. 2-Chloro-N-(2-nitrophenyl)acetamide has luminescence properties that can be exploited to detect the presence of chloride ions at low concentrations.</p>

<p>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.</p>

<p>5-Chloro-2-methoxy-4-methylnitrobenzene is a high quality chemical that can be used as a research chemical, reagent, or a useful scaffold. It is also an intermediate in the synthesis of organic compounds. 5-Chloro-2-methoxy-4-methylnitrobenzene is a versatile building block for the synthesis of other chemicals and has many uses in the pharmaceutical industry. The CAS number for this chemical is 101080-03-9.</p>

<p>Trans-3-Nitrocinnamic acid is a white solid that can be obtained by the nitration of cinnamic acid. Trans-3-Nitrocinnamic acid is an isoenzyme as it has different chemical properties than cis-3-nitrocinnamic acid. The intermolecular hydrogen bonding and vibrational frequencies are different in trans-3-nitrocinnamic acid, which causes the dipole to change and increases the solubility in water. The genotoxic activity of trans-3-nitrocinnamic acid was evaluated using the Ames test, which showed that it is not mutagenic. However, there were some genotoxic effects observed in rats after applying trans-3-nitrocinnamic acid on skin.</p>

<p>1-N-Acetyl-3-nitro-p-phenylenediamine is a hydrolytic product of 1,4-diaminobenzene. It is an intermediate in the preparation of naphthalene diamine and has been shown to hydrolyze in acidic solutions.</p>

<p>5-Chloro-1-methyl-4-nitroimidazole (5C1MI) is a fatty acid that is synthesized by the reaction of phosphorus pentachloride and an aliphatic hydrocarbon. It has been shown to be effective in treating women with breast cancer. 5C1MI blocks the activity of a protein called HER2, which promotes tumor growth. The drug has been shown to cause an increase in the number of circulating lymphocytes and natural killer cells, as well as an increase in the production of antibodies in mice. These effects are likely caused by 5C1MI's ability to inhibit the proliferation of T cells and B cells. 5C1MI has also been shown to have a high solubility in water and low solubility in lipids, which makes it suitable for administration via intravenous injection.</p>

<p>4-Nitrobenzanilide is a synthetic dyestuff that is used to produce a variety of dyes. It is also an inhibitor that has been shown to have amoebicidal activity in vivo and in vitro. 4-Nitrobenzanilide inhibits organisms by reacting with the chloride ion, which is essential for the synthesis of DNA and RNA. The demethylation reaction leads to the formation of hydrogen chloride, which may be responsible for its cytotoxic effects on living cells.</p>

<p>4-Hydroxy-3-nitrophenylacetic acid (4ONPA) is an organic compound that is the product of the reaction between hydroxylamine and nitrobenzaldehyde. It has been shown to have cytotoxicity in breast cancer cells and has been used as a probe for optical imaging studies. 4ONPA has also been shown to be able to inhibit the activity of enzymes such as catalase, peroxidase, and lipoxygenase. The uptake of 4ONPA into cells is dependent on its concentration and the cell type. This drug can be useful for treating degenerative diseases because it inhibits microglia activation by blocking the enzyme phospholipase A2. Clinical trials are currently being conducted for 4ONPA’s potential use in treating herpes simplex virus infections and cancerous lesions associated with Alzheimer's disease.</p>

<p>1-(2,5-Dichlorophenyl)-2-nitroethene is a chemical compound that is used as a research chemical. It's an aromatic organic compound that can be used as a versatile building block for the synthesis of complex compounds. It's also a good intermediate for many fine chemicals. 1-(2,5-Dichlorophenyl)-2-nitroethene has CAS number 1056473-63-2 and is classified as an "Aromatic Organic Chemical".</p>

<p>4-Fluoro-3-nitrobenzonitrile is a potent inhibitor of tyrosine kinase. It binds to the ATP binding site of the enzyme and prevents it from phosphorylating tyrosine residues on other proteins. 4-Fluoro-3-nitrobenzonitrile has been used as a tool in analytical chemistry, where it was shown to be able to detect trace amounts of benzene. This compound has also been shown to have toxicological effects, such as lowered body weight, increased liver weight, and decreased spleen weight. These effects were observed in mice exposed to 4-fluoro-3 nitrobenzonitrile at doses that were well below those needed for lethal toxicity.</p>

<p>3-Nitro-6-pyridinecarboxaldehyde is a colorless liquid that is soluble in water. It has a boiling point of 155 degrees Celsius, and it has a density of 1.03 grams per milliliter. This chemical reacts with metal ions to form nitro compounds. 3-Nitro-6-pyridinecarboxaldehyde has been used as an analytical reagent for the determination of benzenes and pyridines in organic solvents and gas chromatography calibration. The reactivity of this chemical is due to its pyridine ring, which can be used as a ligand or reagent.</p>

<p>2'-Ethoxy-4'-nitroacetanilide is a chemical compound that is used as a building block in the synthesis of other chemicals. It is a versatile building block and can be used to synthesize many different types of compounds, including drugs, pesticides, and dyes. 2'-Ethoxy-4'-nitroacetanilide has been classified as a speciality chemical and is not for human consumption.</p>

<p>L-Methionine 4-nitroanilide is a polymerase chain reaction (PCR) substrate. It has been shown to bind to DNA with calcium and to have protease activity. L-Methionine 4-nitroanilide is a synthetic substrate used in the biochemical study of serine proteases. L-Methionine 4-nitroanilide has been found to be active against P. aeruginosa and thermococcus, but not against mosquitoes. The optimum pH for this compound is 7 and it can be found at a concentration of 10mM in the range of pH 5 - 8.</p>

<p>2-Fluoro-3-nitrobenzoic acid ethyl ester is a versatile, high quality building block with a number of uses in research and industry. It is an intermediate in the synthesis of a range of compounds, including pharmaceuticals and other fine chemicals. 2-Fluoro-3-nitrobenzoic acid ethyl ester is also used as a reagent for the synthesis of complex compounds, such as pharmaceuticals. This compound can be synthesized from readily available starting materials and has been shown to be useful for the preparation of scaffolds for organic synthesis. 2-Fluoro-3-nitrobenzoic acid ethyl ester is not listed on the Chemical Abstract Service (CAS) registry, but it does have an IUPAC name (2-(2,6-difluorophenyl)-5-(1,1,2,2 tetrafluoropropoxy)-3H-[1]py</p>

<p>3-Nitrotyramine is a compound that has catabolic properties. It is the product of tyrosine, which is an amino acid found in most proteins. 3-Nitrotyramine has been shown to be metabolized by humans through the liver and kidneys. The metabolic pathway for this compound starts with the conversion of L-methionine into dl-methionine. This reaction generates a molecule called S-adenosyl methionine, or SAMe, which is involved in many biological processes such as neurotransmitter synthesis and gene expression regulation. 3-Nitrotyramine can also be converted into dopamine by way of the enzyme catecholamine methyltransferase. Dopamine has been shown to have a variety of effects on human physiology, including being involved in mood disorders and motor control. 3-Nitrotyramine can also be converted into gold nanoparticles by means of an acid analysis test.</p>

<p>2,2'-Dinitrobiphenyl is an organic chemical compound that belongs to the class of diazo compounds. It is a white crystalline solid that is soluble in organic solvents such as benzene, ether and chloroform. 2,2'-Dinitrobiphenyl has been used in analytical chemistry as a reducing agent for phosphite and other anion radicals. The reduction products can be analyzed using various techniques such as infrared spectroscopy or electron paramagnetic resonance spectroscopy. It also reacts with amide ions to form nitro or chloride compounds.</p>

<p>2-Fluoro-3-nitrobenzoic acid is a fine chemical that has been used as a building block for research chemicals, reagents, and speciality chemicals. It is also a versatile building block for the synthesis of complex compounds and useful scaffolds. 2-Fluoro-3-nitrobenzoic acid can be used as an intermediate in organic reactions or as a reaction component in the synthesis of pharmaceuticals. This compound has been shown to have high purity and good quality with CAS No. 317-46-4.</p>

<p>Phenyl 4-nitrobenzoate is a polymerized ester with hydroxy groups and phosphorus oxychloride as the raw material. It is synthesized by heating ethyl esters in trifluoroacetic acid, which reacts with nitric acid and phosphorus oxychloride. The compound is an amide with a bond cleavage activation energy of 109 kJ/mol. The kinetic of the reaction was determined by measuring the time it took for the reaction to reach certain levels. Phenyl 4-nitrobenzoate has been shown to be able to activate supramolecular assemblies, leading to new catalytic processes such as hydrogenation, oxidation and reduction reactions.</p>

<p>Please enquire for more information about 3-(tert-butyl)-2-methyl-6-nitroindeno[3,2-c]pyrazol-4-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl 4-nitrophenyl carbonate is a fine chemical that is used as a building block for the synthesis of complex compounds. It is an intermediate in the synthesis of 3,4-Dihydroquinazolinone. This compound has been reported to have useful pharmacological activity and has been used as a research chemical and in the synthesis of pharmaceuticals. (5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl 4 nitrophenyl carbonate also has potential as a reagent and can be used in organic synthesis.</p>

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

<p>3-Methoxy-4-nitroacetophenone is an enamine that can be used in the synthesis of a variety of organic compounds. It is a good reducing agent and can be used to synthesize nitrophenols and nitrosamines. Catalytic hydrogenation, transfer hydrogenation, and reductive condensation reactions all use 3-methoxy-4-nitroacetophenone as a starting material. It has been shown to react with a range of alcohols to form acetals, which are stable compounds with a protective group on the alcohol. Cyclization reactions using 3-methoxy-4-nitroacetophenone have also been reported. This compound has been crystallized in pure form.</p>

<p>Please enquire for more information about 1-(4-Acetoxyphenyl)-2-nitropropene including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Bromo-2-fluoro-5-nitroacetanilide is a versatile building block that has been used in the synthesis of complex compounds. It is a reagent which can be used in the research and development of pharmaceuticals, agricultural chemicals, and other specialty chemicals. 4-Bromo-2-fluoro-5-nitroacetanilide is also a useful building block for synthesis of other chemical compounds. This compound has been shown to have high quality for use in organic synthesis and as a reaction component for the preparation of useful scaffolds. This compound is also useful as an intermediate in organic reactions. CAS No. 95635-46-4</p>

<p>3-Amino-5-nitroindazole is an anticancer drug that inhibits the growth of cancer cells. It has been shown to inhibit the growth of cancer cells by blocking the synthesis and repair of DNA, leading to cell death. 3-Amino-5-nitroindazole also blocks the production of new proteins, which are needed for cell division. This drug also acts on pathways that are important for tumor development and progression, such as signaling pathways and transcription factors. This compound has been shown to be selective against human squamous cell carcinoma cells and has been studied in combination with other anticancer drugs in clinical trials.</p>

<p>Ethyl 3-hydroxy-2-nitrobenzoate is a versatile building block in organic synthesis. It is a useful intermediate that can be used for the synthesis of complex compounds, research chemicals and reagents. It is also a useful scaffold for the synthesis of fine chemicals, and has been used as a reaction component in high quality chemical reactions.</p>

<p>4-Iodo-3-nitroanisole is an intermediate in the synthesis of 4-methoxy-2-nitroaniline. It is obtained by a cross coupling reaction between 2,4,6-trinitrophenylacetonitrile and 4-iodoaniline. The reductive radical species are generated by the addition of sodium borohydride to the nitro group on the ring. The sequential process entails the formation of the chiral ligand with copper(II) chloride and its adduct with ethyl acetate. This product can be used in cyclic voltammetry experiments as a substrate for cyclic voltammetric studies.</p>

<p>4-Methoxy-3-nitrobenzoic acid is a hydroxybenzoic acid, and belongs to the group of heterocyclic compounds. It is a preactivated hydroxybenzoate that can be used in the synthesis of griseoluteic acid with chloride as an electron donor. Griseoluteic acid has inhibitory activities on isolated yield. This compound also has potent antitumor activity, which may be due to its ability to inhibit DNA synthesis and protein synthesis by binding to DNA polymerase and ribosomes respectively. Preparative high performance liquid chromatography (HPLC) using this compound is possible with marine microorganisms as the stationary phase. The x-ray absorption spectrum shows that 4-methoxy-3-nitrobenzoic acid has potential for use as a contrast agent for x-rays in imaging tissues.</p>

<p>1-(2,5-Dimethoxyphenyl)-2-nitroethane is a versatile building block that can be used as a reagent in organic synthesis or as an intermediate in the manufacturing of other chemicals. It is soluble in most common solvents and has a greenish yellow color. This chemical is also useful for the manufacture of pharmaceuticals, insecticides, and pesticides.</p>

<p>2-Methoxy-5-nitrophenol (2MNOP) is a compound that has been shown to inhibit the growth of bacteria in nutrient solutions by reducing the activity of glutamate pyruvate transaminase and pyridoxine hydrochloride. 2MNOP is a potent inhibitor of bacterial enzyme activities, such as neutral ph, hydrochloric acid, nitro, and toxicity studies. It is not active against eukaryotic cells or plants. The uptake of 2MNOP is enhanced by the presence of diamine tetraacetic acid and ethylene diamine. 2MNOP has also been shown to be effective against multi-walled carbon nanotubes.</p>