Ciano-, Nitrile-

<p>3-Methoxy-4-methylbenzonitrile is a reagent that is used in the synthesis of complex compounds, such as pharmaceuticals and fine chemicals. It has been shown to be useful as an intermediate for the synthesis of various drugs, including antibiotics. 3-Methoxy-4-methylbenzonitrile has also been shown to be a useful scaffold for the synthesis of new drugs and other chemical compounds. This compound is listed on the Chemical Abstracts Service registry number 3556-60-3.</p>

<p>5-Cyano-2-fluorobenzoic acid is a macrocyclization agent that is used in the synthesis of 16-membered macrocycles. It is a nucleophilic reagent that reacts with an electrophile to form a 5,5'-bifluoro-2,2'-dioxodibenzofuranone. This reaction can be performed under mild conditions and proceeds via a 1,4-addition mechanism. The product has two stereogenic centers and four stereoisomers that are formed by the relative configuration of these centers. 5-Cyano-2-fluorobenzoic acid also has application in the clinic as an analogue for fluoroquinolones.</p>

<p>5-Methoxyindole-3-acetonitrile is a synthetic compound used as a reference for the synthesis of melatonin. It is produced by the addition of magnesium to 5-methoxyindole, followed by reaction with cyanide and nitrile. The synthesis of this compound was first published in 1938 and has since been used as a reference for many other studies. It has been shown that 5-methoxyindole-3-acetonitrile has high performance liquid chromatography properties, with a linear range from 0.5 to 50 mg/mL and an ultraviolet spectrum that falls within the region between 220 nm and 400 nm. A molecular modeling study was conducted on this compound, which showed that it conforms with 4-hydroxy indole ring systems found in natural products such as tryptophan and serotonin. This product also has fluorescent properties, which are caused by its electron withdrawing group (cyano).</p>

<p>Please enquire for more information about Barium tetracyanoplatinate(II) hydrate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Adamantyl acetonitrile is a trifluoroacetic acid derivative that is used in the synthesis of 4-aminoantipyrine, chlorides, acid chlorides, and acetonitrile. 1-Adamantyl acetonitrile can be used to produce a variety of pharmaceuticals, such as aliphatic carboxylic acids, aldehydes, and amide. It can also serve as a reactant for reactions with alcohols or amines.</p>

<p>Cypermethrin is an insecticide that belongs to the family of chemical pesticides. It is used in agriculture and in public health to control malaria-transmitting mosquitoes, head lice, and scabies mites. Cypermethrin disrupts the insect nervous system by inhibiting the function of synapses between nerves, resulting in paralysis and death. The compound also affects signal pathways that regulate locomotor activity and enzyme activities. Cypermethrin has been shown to have a high resistance to degradation by glycol ethers such as ethylene glycol monomethyl ether acetate (EGMEA). It has an optimum concentration of 0.01 ppm for mosquito control and 0.1 ppm for lice control. The analytical method involves liquid chromatography with sodium citrate as an ion-pairing agent and a linear calibration curve using a standard curve generated from known concentrations of cypermethrin.</p>

<p>2,5-Dimethoxybenzonitrile is a polymerized organic compound that belongs to the class of benzene compounds. It is a monomer with two methyl groups on either side of the benzene ring. 2,5-Dimethoxybenzonitrile has been studied in terms of its transition and optimization properties using techniques such as IR and NMR spectroscopy. The frequencies of the chemical bonds have been analyzed, and it has been found that the molecule is centrosymmetric. 2,5-Dimethoxybenzonitrile can also be used to form polymers with other molecules by linking them together through covalent bonds.</p>

<p>4-Cyanobenzylamine HCl is a degradable polymer that has been shown to inhibit colonic adenocarcinoma in mice. This compound was synthesized by the reaction of 4-cyanobenzylamine with 3-mercaptopropionic acid and was characterized using IR, 1H NMR, and 13C NMR spectroscopy. It also showed an inhibitory effect on the proliferation of human colon cancer cells. The polymer was found to gel when mixed with different concentrations of acrylamide and methylene bisacrylamide. Gelation occurred at a lower concentration of acrylamide than the amount used in previous studies. This may be due to its functional groups and morphology, which could have contributed to the inhibition of cell growth.</p>

<p>4-Cyano-L-phenylalanine is an unnatural aminoacid that has been shown to bind to amyloid protein, which is associated with Alzheimer's disease. The binding of 4-Cyano-L-phenylalanine inhibits the synthesis of amyloid protein and prevents the formation of amyloid fibrils. 4-Cyano-L-phenylalanine also irreversibly inhibits the enzyme responsible for the production of hydrochloric acid in bacteria. The x-ray crystal structures of 4-Cyano L-phenylalanine have been determined and show that this compound binds to the active site of the enzyme synthetase, preventing it from forming an amino acid bond. 4-Cyano L-phenylalanine is an analog of 4-L-phenylalanine and, thanks to its cyano (nitrile) group, is a good candidate for use as a fluorescence marker to study the peptide membrane interactions.</p>

<p>Please enquire for more information about [3-(2-Methylphenyl)-1,2,4-oxadiazol-5-yl]acetonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Benzenesulphonylacetonitrile is an alkanoic acid nucleophile with a benzimidazole derivative. It has shown potential for use as a cancer drug by inhibiting tumor-associated enzymes and inducing apoptosis in cancer cells. Benzenesulphonylacetonitrile is also active against inflammatory diseases such as rheumatoid arthritis, psoriatic arthritis, and Crohn's disease. This drug can be synthesized by the reaction of sodium salts with benzenesulphonylacetone followed by a nucleophilic substitution reaction with methylene chloride. The synthesis of benzenesulphonylacetonitrile requires anhydrous acetonitrile and palladium-catalyzed coupling reactions in the presence of sodium carbonate. Benzenesulphonylacetonitrile has chemical stability in the presence of acids, bases, and heat.br&gt;</p>

<p>2,6-Dichlorophenylacetonitrile (2,6-DCPA) is a cyanide herbicide that controls weed growth. 2,6-DCPA is used as a preemergent herbicide and is applied to the soil before planting. It can be mixed with calcium oxide or other materials to form a dust, which is then applied to the soil surface. 2,6-DCPA inhibits plant growth by interfering with the photosynthesis process, which may be due to its high cytotoxicity. The exact mechanism of action has not been determined but it may be due to interference with chloride transport or ethyl esters production in plants. This chemical has also been shown to inhibit amine metabolism in plants and animals.<br>2,6-DCPA has two isomers: cis and trans. They differ only in the position of the chlorine atom on the benzene ring: cis (left) and trans (right).</p>

<p>3-Methyl-4-nitrobenzonitrile is a fluorescing aromatic amine that is synthesized by aliphatic amines. It has been shown to inhibit the growth of cells in culture, which may be due to its ability to bind with and inhibit the insulin-like growth factor receptor-1 (IGF-1R). 3-Methyl-4-nitrobenzonitrile has also been shown to bind with cytochrome P450 enzymes, where it can be oxidized or reduced. The conformation of 3-methyl-4 nitrobenzonitrile is dependent on the solvent molecules present.</p>

<p>Dodeca 2E,4E,8Z,10E,Z-tetraenoic acid isobutylamide (DETBA) is a versatile building block that is used in the synthesis of natural products and pharmaceuticals. DETBA can be used as a reaction component in organic synthesis to form complex compounds such as polyesters, polyamides, polyurethanes, and polyimides. It also has high quality and can be used in research or speciality chemical applications.</p>

<p>3-Amino-4-methylbenzonitrile is an organic compound that is produced by the oxidative dehydrogenation of 3,4-dimethylaniline. It has been shown to undergo a number of reactions, including hydrochloric acid transfer hydrogenation and diazotization. This reaction yields 3-amino-4-methylbenzonitrile, dimethylamine and anilines. The transfer hydrogenation of nitroarenes with 3-amino-4-methylbenzonitrile gives 3-(3,4)-diaminobenzonitrile and 2,6-dinitrotoluene. The optimization of this reaction has led to the discovery of new nitrite derivatives as a result of the addition of nitrite in the presence of 3-amino-4-methylbenzonitrile.</p>

<p>4-Chloro-3-nitrobenzonitrile is a molecule with potent antibacterial activity. It is synthesized by the reaction of sodium carbonate, hydrogen chloride, and 4-chlorobenzonitrile. 4-Chloro-3-nitrobenzonitrile has shown antimicrobial properties against a wide range of bacteria, including methicillin resistant Staphylococcus aureus (MRSA) and Enterococcus faecium. This compound has been used in the treatment of infections caused by these bacteria. 4-Chloro-3-nitrobenzonitrile also has the ability to inhibit the synthesis of fatty acids and lipids in bacterial cells, which may be responsible for its antimicrobial effects.</p>

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<p>2-Chloro-3-methylbenzylamine HCl is a fine chemical that is a versatile building block for synthesis of pharmaceuticals and research chemicals. It is also a useful intermediate in the production of other compounds, such as speciality chemicals, complex compounds, and reaction components. 2-Chloro-3-methylbenzylamine HCl has many potential applications in both academia and industry because it is a high quality reagent with many uses.</p>

<p>Substrate of benzylamine oxidase and monoamine oxidase B</p>

<p>4-Amino-2-cyanotoluene is a quinazoline compound that inhibits the synthesis of thymine, which is necessary for DNA replication. This compound binds to the enzyme thymidylate synthetase, thereby inhibiting the synthesis of thymine. The inhibitory effect has been shown in a study using calf thymus DNA. 4-Amino-2-cyanotoluene also inhibits the synthesis of other nucleic acids such as adenine and guanine.</p>