Nitro

<p>Applications 4-Nitro-benzeneethanol is a useful synthetic intermediate. It can be used to synthesize N-phenylethylindole carboxamides as SAR study of allosteric modulators of CB1 receptor. It can also be used to prepare 2-aza-2'-deoxyinosine-containing oligodeoxyribonucleotide duplexes.<br>References Piscitelli, F., et al.: J. Med. Chem., 55, 5627 (2012); Acedo, M., et al.: J. Org. Chem., 60, 6262 (1995)<br></p>

<p>Applications 5-Nitroanthranilonitrile (cas# 17420-30-3) is a useful research chemical.<br></p>

<p>Applications A related compound of 1,2,3-benzothiadiazoles as synergists against the housefly (M. domestica).<br>References Gil, D.L., et al.: Pesticide Biochem. Physiol., 6, 338 (1976),<br></p>

<p>Applications 3-Hydroxy-2-nitrobenzoic Acid (cas# 602-00-6) is a compound useful in organic synthesis.<br></p>

<p>Impurity Vildagliptin Impurity<br>Applications 1-Amino-3-nitroadamantane has potential application in co-catalyst for transition metal reactions and maybe a useful intermediate for the synthesis of Vildagliptin (V305000), an antidiabetic drug that inhibits dipeptidyl peptidase 4 (DPP-4). Vildagliptin exhibits antioxidant properties and may be an apoptotic compound against pancreatic cancer cells.<br>References Amritha, C., et al.: JCDR 9, FC14 (2015); Ahren, B., et al.: J. Clin. Endocrinol. Metab., 89, 2078 (2004), Ahren, B., et al.: Diabetes Care, 27, 2874 (2004), Barlocco, D., et al.: Curr. Opin. Invest. Drugs, 5, 1094 (2004)<br></p>

<p>Applications Methyl 2-fluoro-3-nitrobenzoate<br></p>

<p>Applications N-​(3-​Dibenzofuranyl)-​5-​nitro-2-​furancarboxamide is synthesized from Dibenzo[b,d]furan-3-amine (D418205), which is a building block used as a reactant in the preparation of dibenzofuryl(phosphonomethyl)alanines as endothelin converting enzyme inhibitors.<br>References De Lombaert, S., et al.: J. Med. Chem., 43, 488 (2000);<br></p>

<p>Applications 4-Dimethylamino-4'-nitrostilbene (cas# 4584-57-0) is a useful research chemical.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>

<p>6-Amino-5-nitroso-2-thiouracil is a water molecule that has been synthesized and characterized by the kinetic method. It has an intense absorption line at 514 nm and can be used as a marker for technetium. 6-Amino-5-nitroso-2-thiouracil is also a ligand, which is a chemical that binds to metal ions in order to form coordination complexes. 6-Amino-5-nitroso-2-thiouracil is formed by the reaction of chloramine with ammonia, as well as other reactions involving chlorine atoms. 6Amino - 5 nitroso - 2 thiouracil can be used as a chelate ring, which is a type of ligand that contains both nitrogen and sulfur atoms. Bleomycin, a five membered ring molecule, reacts with 6 amino - 5 nitroso - 2 thiouracil to</p>

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<p>3-Chloro-4-nitropyridine 1-oxide is the condensation product of 2-chloro-3-nitropyridine and nitric acid. 3-Chloro-4-nitropyridine 1-oxide has an isomeric nature and can be purified by recrystallization from water. The compound has a molecular weight of 286.1 g/mol and a monoclinic crystal structure. It has two n-oxides, which are isomers of each other, with nmr spectra that differ by the shift in the chemical shifts of the protons on the aromatic ring. 3-Chloro-4-nitropyridine 1-oxide condenses with lanthanides to form lanthanide complexes, such as Eu(III)(3,5'-ClO 4 ) 2 . This compound is also used in the synthesis of phenoxathiine derivatives that have antihypertensive activity.</p>

<p>2,4-Difluoro-5-nitrobenzonitrile is a chemical that has been found to have affinity for the central nervous system. It inhibits the reuptake of monoamines such as dopamine and serotonin. This chemical has been shown to be endogenously produced in humans and animals. 2,4-Difluoro-5-nitrobenzonitrile also inhibits the uptake of amines by blocking the activity of their respective transporters. The compound is an isomeric mixture of two possible structures, which differ in their position on the benzene ring. The first form is characterized by a low affinity for neurotransmitter receptors and therefore has low inhibitory properties on monoamine uptake. The second form has greater affinity for neurotransmitter receptors and therefore has greater inhibitory properties on monoamine uptake, although at higher concentrations it may lead to adverse effects on muscle tissue.</p>

<p>4-Fluoro-3-nitrophenylacetonitrile is a monomer that can be synthesised from the reaction of carbamic acid and diphenyl ether. It is chiral, stereoselective and nucleophilic. 4-Fluoro-3-nitrophenylacetonitrile can also be synthesised by reacting fluoroacetamide with sodium cyanide in water, forming the corresponding amide, which reacts with acetonitrile to form the nitro compound. The anti-cancer properties of 4-fluoro-3 nitrophenylacetonitrile have been studied in vitro and in vivo. This substance has been shown to inhibit growth of cancer cells and induce apoptosis. In addition, this substance has been used as a synthetic strategy for dihydroisoquinolines, which are important for their anti-cancer properties.</p>

<p>N-Nitroso guvacoline is a nitrosated guvacoline analog that is used to induce cancer in animals and as an experimental tool for studying the role of acetylcholine in lung cancer. N-Nitroso guvacoline has been shown to inhibit the growth of bacteria such as typhimurium and nadph-cytochrome p450 in the presence of fatty acids, suggesting that it may be genotoxic. The carcinogenic effects of N-nitrosoguvacolin were studied using Sprague-Dawley rats exposed to this agent by inhalation. The rats were found to have increased levels of urinary nitrite and nitrate, which are products from the metabolism of N-nitrosoguvacolin.</p>

<p>N,N-Dimethyl-2-nitroaniline is a colorless liquid with a characteristic odor. It has a boiling point of 170 degrees Celsius and a melting point of -10 degrees Celsius. The molecule is composed of two nitro groups and one methyl group, which are in an ionic bond. N,N-Dimethyl-2-nitroaniline can be found in solvents such as hexane or benzene and has an intramolecular hydrogen bonding frequency of 3.4 GHz. This compound is soluble in water and ethanol, but insoluble in ether.</p>

<p>N-Nitrososarcosine is a nonsteroidal anti-inflammatory drug (NSAID) that belongs to the group of ester hydrochloride. It inhibits the synthesis of prostaglandins, which are chemical mediators of inflammation and pain. N-Nitrososarcosine has been shown to be effective for the treatment of arthritis in animal models. In vitro studies have shown that this drug inhibits polymerase chain reaction and can be used for genotyping bacterial DNA. N-Nitrososarcosine has been found in urine samples from patients with autoimmune diseases, as well as in pharmaceutical preparations. The use of this drug as a model system for studying enzyme hydrolysis has also been studied.</p>