Nitro

Please enquire for more information about N-(4-Nitrobenzoyl)-D-glutamic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Diethylnitroterephthalate (DENP) is a pyridyl-based substance that attacks the esters of medication. The process of the attack is reversible, which means that DENP can be used as a neutralizer. It has been shown to be able to filter out drugs in water and other liquids. It is also theorized that DENP can be used as a diagnostic agent for the detection of drugs and their metabolites in urine. The selectivity of DENP has been shown by its ability to selectively detect amphetamine from other substances such as morphine or codeine. This characteristic has made it possible for researchers to patent DENP for this use.

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Methyl 4-chloro-3-methoxy-5-nitrobenzenecarboxylate is a drug that has been shown to be activated by the body's endogenous enzymes. It is a potent stimulator of mononuclear cells and endoplasmic reticulum, which are involved in the production of substances such as lymphokines, leukotrienes, and prostaglandins. Methyl 4-chloro-3-methoxy-5-nitrobenzenecarboxylate has been shown to inhibit the growth of colon tumors in mice through its ability to induce apoptosis. This drug also has a pharmacokinetic profile that makes it suitable for oral administration. The drug is rapidly absorbed and metabolized by the liver into inactive metabolites, with an elimination half life of about 3 hours. It binds to DNA with high affinity and inhibits transcriptional activity through competitive inhibition of DNA binding at the promoter region.

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

Piperidine is a chemical compound that has the chemical formula CH3CONH2. It is a colorless, water-soluble liquid with an ammonia-like odor. Piperidine reacts with many other compounds in chemical reactions to form piperidines, which are used in the manufacture of pharmaceuticals, dyes, pesticides, and rubber products. The molecule is planar and all three N-H bonds are equivalent, which indicates that it is not chiral. Piperidine has been shown to react with chlorine and chloramine under conditions of microwave irradiation to produce 2-chloro-4,6-dihydroxy-5-nitropyrimidine (2CDNP). This reaction was found to be efficient at low temperatures and atmospheric pressure. 2CDNP has also been shown to be reactive with nitro groups in molecules such as aniline hydrochloride or benzene diazonium chloride to form nitroso derivatives. These reactions were found

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

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2-Amino-3,5-dinitrothiophene is an organic compound that is used in dyestuffs and other chemical processes. It has been shown to be a chromophore, which is the light-absorbing part of a dye molecule. 2-Amino-3,5-dinitrothiophene has also been used in toxicity studies as a solvent for anilines, amines, and heterocyclic amines. The molecule's nucleophilic attack on diazonium salts leads to the formation of heterocycles. 2-Amino-3,5-dinitrothiophene can be used as a dyebath additive in cellulose acetate fiber production to increase the color intensity of the fibers. This compound has optical properties that are determined by its molecular structure and shape.

Please enquire for more information about 2-[4-(2-Furoyl)piperazin-1-yl]-5-nitrobenzonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

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2-Amino-3-nitrophenol is an inhibitor of matrix metalloproteinases that is active against a broad spectrum of pro-inflammatory and destructive enzymes. It has been used to inhibit the activity of matrix metalloproteinases in vitro and in vivo, with a wide range of applications in the fields of biochemistry, cell biology, and medicine. This compound has been shown to be effective against type strain C. albicans and C. glabrata strains, as well as other fungi such as Aspergillus niger, A. fumigatus, A. terreus, and A. flavus. 2-Amino-3-nitrophenol may have antifungal activity due to its ability to inhibit the synthesis of hyaluronic acid by these fungi. 2-Amino-3-nitrophenol is an inhibitor of matrix metalloproteinases that is active against

2-Bromo-4-methyl-1-nitrobenzene is an organic compound that reacts with nucleophiles. It has been used as a substrate for the dehydrating agent and the dehydrated product can be used in the synthesis of nucleosides and other compounds. 2-Bromo-4-methyl-1-nitrobenzene can react with chloride to form a mononucleotide, which can then be reacted with arsenical to produce methylbenzenes. It is also used in the synthesis of flavonoids and flavones, which are natural phenols found in plants that have antioxidant properties.

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4-Nitro-2-(trifluoromethyl)benzenol is a hydrophobic chemical compound. It has been used as a reactant in the synthesis of other chemicals, such as 2-fluoro-5-nitrobenzotrifluoride and hexadecanoic acid. 4-Nitro-2-(trifluoromethyl)benzenol has been shown to exist in two different forms, depending on the solvent it is dissolved in. In aqueous solvents, it exists as an unstable solution that can be converted to an insoluble form by adding camphor. The addition of camphor changes the surface properties of 4-Nitro-2-(trifluoromethyl)benzenol, which promotes the conversion from one isomer to another. 4 Nitro-2-(trifluoromethyl)benzenol has also been found to react with light through

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2,4-Dichloro-6-nitrophenol is an organic compound that is used as a pharmaceutical preparation. It is also used in the preparation of other compounds for industrial use. 2,4-Dichloro-6-nitrophenol has been shown to be phototransformed by light to form 2,4-dichlorophenol and 4-chlorophenylhydrazine. A predictive model was developed using linear regression analysis to describe the relationship between the concentration of 2,4-dichloro-6 nitrophenol and the growth rate of bacterial cells in a model system. The model can be used to predict the growth rate of bacterial cells exposed to different concentrations of 2,4-dichloro-6 nitrophenol. 2,4-Dichloro-6 nitrophenol also reacts with hydrogen gas in a reaction that is proportional to its concentration, which leads to a decrease in

alpha-Chloro-3-nitrobenzaldoxime is an antimicrobial agent that belongs to the group of itraconazole. It is a synthetic compound that was synthesised for its anti-fungal properties. alpha-Chloro-3-nitrobenzaldoxime has been shown to be effective against candida albicans and other fungi, which may be due to its ability to inhibit the production of 1,3-dipolar cycloaddition products from aldehydes. alpha-Chloro-3-nitrobenzaldoxime also inhibits the synthesis of proteins and RNA by inhibiting protein synthesis at the ribosome level. This drug can be used in conjunction with fluconazole for more efficient antifungal activity.

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.

1-(3-Methylphenyl)-2-nitroethene is a nitro compound that can be synthesized by the reduction of nitrobenzene with sodium, potassium, or calcium in the presence of carbon monoxide. It has been shown to be an efficient reductive agent for carbonyl compounds and multisubstituted ketones. Nitration of 1-(3-methylphenyl)-2-nitroethene with sulfuric acid gives 1-(3-methylphenyl)-2-nitrophenol.

3-Nitrophenoxyaceticacid is a molecule that contains a nitro group and an acid group. It has a molecular weight of 126.2 g/mol and a chemical formula of C6H5NO2O3. 3-Nitrophenoxyaceticacid can be synthesized from phenol, nitric acid, and acetic acid in the presence of iron oxide as a catalyst. The molecule has two functional groups: the nitro group and the carboxylic acid group. 3-Nitrophenoxyaceticacid has been shown to have hydratropic properties due to its ability to form hydrogen bonds with other molecules in water. This molecule also reacts with chlorine in water, forming hydrochloric acid (HCl). 3-Nitrophenoxyaceticacid is insoluble in water but soluble in ethanol and acetone. The molecular weight of this molecule is 126.2 g/mol, which corresponds to its molar mass of

o-Nitrophenyl benzyl ether is a cell membrane ionophore that has been used to measure the chloride transport by escherichia coli cells. It is an anionic compound that produces a color change in response to the chloride concentration. The uptake of o-nitrophenyl benzyl ether can be monitored by measuring the intensity of light passing through the solution. This process is called ion-selective spectrophotometry. The use of this agent as a cell membrane ionophore is limited to short-term experiments, since it will break down over time and may produce false results. The solvents used for this chemical are benzyl alcohol, pentane, and triethylamine.

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

3,3'-(Carbonyldiimino)bis[4-methoxy-6-nitrobenzenesulphonic] acid is a yellow-orange powder that has been shown to have carcinogenic activity. It is used for the detection of nitro compounds in water and wastewater. 3,3'-(Carbonyldiimino)bis[4-methoxy-6-nitrobenzenesulphonic] acid has been found to be carcinogenic in bioassay studies using rats and mice. Nitro compounds are classified as carcinogens by the International Agency for Research on Cancer (IARC).

8-Chloro-5-nitroquinoline (8CNP) is a bacteriostatic and antimicrobial agent that belongs to the group of quinoline derivatives. It is used as an aliphatic, pharmacological and medicinal agent. 8CNP has been shown to inhibit the growth of bacteria by binding to their DNA. This compound has been synthesized in the laboratory and its affinity for 5-HT2c receptors has been studied using radioligand binding assays. 8CNP also inhibits the synthesis of neurotransmitters in rats, which may be due to its ability to bind to these receptors. 8CNP is an aliphatic, pharmacological, medicinal agent that has been shown to inhibit bacterial growth by binding to their DNA.

Please enquire for more information about 2-Chloro-6-methyl-5-nitro-4(1H)-pyrimidinone including the price, delivery time and more detailed product information at the technical inquiry form on this page

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4-Nitrobenzaldehyde is a reactive compound that has been shown to have antimicrobial activity. It is used in the synthesis of antibiotics and other pharmaceuticals. 4-Nitrobenzaldehyde binds to the mitochondrial membrane potential, which leads to the disruption of aerobic respiration. This compound has also been shown to bind to human serum proteins, such as albumin. The mechanism of this binding is through hydrogen bonding interactions with the amine groups on the protein surface. The reaction of 4-nitrobenzaldehyde with sodium carbonate results in an equilibrium between nitrobenzene and 4-nitrophenol. The equilibrium constant for this reaction can be determined experimentally by measuring the solubility of these compounds at different concentrations. 4-Nitrobenzaldehyde can be used as a model system for studying electron transfer reactions in electrochemistry through its interaction with methyl ethyl ketone (MEK) and pyridine (PYR). MEK

Please enquire for more information about 4-(2-methyl(8-quinolyloxy))-1-nitrobenzene including the price, delivery time and more detailed product information at the technical inquiry form on this page

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C2'-Chloro-2-(4-nitrophenyl)cinnamonitrile is a fine chemical that is used as a reagent and building block in the synthesis of other compounds. C2'-Chloro-2-(4-nitrophenyl)cinnamonitrile has been shown to react with various reagents to form useful intermediates and speciality chemicals. It can be used as a versatile building block in the synthesis of complex compounds.

Please enquire for more information about 6-Nitro[1,2,4]triazolo[4,3-a]pyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page

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N,N-Dinitroso-p-phenylenediamine-N,N-diacetic acid (DNPD) is a water soluble molecule with a pyrimidine nucleus. It has been shown to have anti-inflammatory properties and is used for the treatment of skin conditions such as psoriasis. DNPD also modulates the apoptotic process by inhibiting the proliferation of endothelial cells. DNPD induces apoptosis in human keratinocytes by activating soluble guanylate cyclase, which leads to an increase in intracellular levels of guanosine 3',5'-cyclic monophosphate (cGMP). The activation of cGMP leads to an increase in the production of reactive oxygen species and mitochondrial dysfunction. This ultimately results in cell death.

Please enquire for more information about N-(2-Nitrophenyl)propane-1,3-diamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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4-Iodo-2-nitrotoluene is a chromatographic solvent. It is used in analytical techniques primarily for the separation of amines and anilines. 4-Iodo-2-nitrotoluene is also used to extract solvents from wastewater, yielding a constant yield of pentanes. The solvent effect can be analyzed using various techniques, such as solvents extraction and gas chromatography. 4-Iodo-2-nitrotoluene also has use in the analysis of anilines by capillary gas chromatography or high performance liquid chromatography.

1-(3-methylphenyl)-2-nitropropene is a versatile building block that is used in the synthesis of complex compounds. It is also an intermediate for the synthesis of other chemicals, such as reaction components and useful scaffolds. It has been shown to be high quality and useful as reagent and speciality chemical.

Applications 4-Nitrocatechol can be used as a catalyst and an antibacterial against intestinal bacteria. References Jones, Matthew D., et al.: Polymer Preprints (Amer. Chem. Soc.), 48(2), 873-874 (2007);Jeong, Eun-Young, et al.: Food Chem.,  115(3), 1006-1010 (2009)

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3,5-Dinitrobenzylchloride is a chemical compound that belongs to the family of phenylchloroformates. It is an aminoacylated derivative of subtilisin and was synthesized by reacting 3,5-dinitrobenzyl chloride with glutamate in methanol. The reaction yielded a mixture of two products: one with an aminoacyl group at the C-terminal end and the other without. The latter product contains a carbonyl group at the C-terminal end instead. 3,5-Dinitrobenzylchloride has been used as a reagent for detection of proteins with high sensitivity by gel electrophoresis. It also has thermal expansion properties that are greater than those of chromatography columns, which makes it useful in supramolecular chemistry or spectrometric analysis where these properties may be advantageous. 3,5-Dinitrobenzylchloride is not effective against methyl ketones

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Applications Methyl 4-nitrobenzoate (cas# 619-50-1) is a useful research chemical.

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5-Fluoro-2-nitrobenzotrifluoride is a triamine that stabilizes complex molecules. It has been used in the synthesis of fluorinated compounds and as a nucleophile in organic reactions. The amido group, which is present on 5-fluoro-2-nitrobenzotrifluoride, reacts with electrophilic carbon atoms to form new bonds. This type of reaction is known as an amido substitution. 5-Fluoro-2-nitrobenzotrifluoride is also able to react with sodium nitrate to form a nitro group, which can be used for the synthesis of nitro compounds. As a result, this chemical has been used as a waveguide material in the fabrication of microns and operational amplifiers.

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2-Methyl-5-nitrobenzoic acid is a synthetic compound that has been shown to inhibit the growth of tumor xenografts in mice. This compound has been shown to inhibit the production of prostate-specific antigen and prostate cancer cells, as well as cause apoptosis in prostate cancer cells. 2-Methyl-5-nitrobenzoic acid also inhibits the activity of vitamin D3 and docetaxel, which are both chemotherapeutic agents used to treat prostate cancer. 2-Methyl-5-nitrobenzoic acid is a thermodynamic inhibitor with an IC50 value of 0.1 mM. It is an inhibitor of cellular respiration and mitochondrial function with a Km value of 1 mM. This agent also inhibits tumor perfusion, which may be due to its ability to induce apoptosis in tumor cells.

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2-Formyl-4-Nitrophenyl 2-Chloro-6-Fluorobenzoate is a 5HT7 receptor antagonist that can be used to treat bowel syndrome. It has high binding affinity for the 5HT7 receptor and shows antinociceptive activity in animal models of colorectal pain. The drug also binds with high affinity to the 5HT7 receptor, which is expressed on neurons in the enteric nervous system and has been implicated in the pathophysiology of bowel syndrome (IBS).

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Piperazine is a chemical compound that is used as an insecticide and herbicide. It is also a part of the structure of the neurotransmitter dopamine. Piperazine has been shown to inhibit the reuptake of dopamine by blocking the dopamine transporter protein, which leads to increased extracellular concentrations of dopamine. This increase in dopamine can be simulated using molecular modelling techniques. The 3-nitrophenylacetyl chloride moiety on piperazine has been analysed using high-resolution simulations and crystallographic data to help understand its activity in inhibiting the dopamine transporter.

4-Chloro-7-nitroquinazoline is an organic compound that is used as a mutagen. It is not active against typhimurium bacteria, but has been shown to be mutagenic in other experiments. 4-Chloro-7-nitroquinazoline can be used to produce nitrosamines by reacting with amines or formamide. This chemical has also been shown to be mutagenic in the presence of hydrochloric acid and magnetic fields. 4-Chloro-7-nitroquinazoline can also react with chloride and phosphorus pentachloride to form chlorides, which are known carcinogens. It has been shown to inhibit the growth of cells in culture when used at high concentrations, but does not have any effect on cells at low concentrations.

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