Cyano-, Nitrile-

<p>2-Bromophenylacetonitrile is a synthetic compound that is used in wastewater treatment. It is effective at removing cyanides, phenylpropionic acid, and aldehydes from wastewater. 2-Bromophenylacetonitrile has been shown to be an efficient method for the removal of liriodenine from sewage water and for the removal of 2-bromostyrene from industrial waste water. This process can be used as an analytical method to measure the concentration of these substances in samples of wastewater. The reaction mechanism involves the formation of a nitrilium ion intermediate and subsequent reactions with alcohols to form esters or ethers.</p>

<p>2-(2,3-Dichlorophenyl)-2-guanidinyliminoacetonitrile (2,3-DCPP) is a high quality reagent that is used in the preparation of complex compounds. It is also an intermediate in the synthesis of fine chemicals and useful scaffold and building block for research chemical. 2,3-DCPP has been shown to react with a variety of functional groups including amines, alcohols, thiols, carboxylic acids, organometallic reagents and many others. It is also a versatile building block for the synthesis of chemical substances such as pharmaceuticals, agrochemicals or dyes.</p>

<p>Ethyl cyanoglyxylate-2-oxyme potassium salt is a high quality reagent for the production of complex compounds that can be used in fine chemicals, pharmaceuticals, and other speciality chemicals. It has been shown to be an intermediate for the synthesis of useful scaffolds and building blocks. The CAS number is 158014-03-0. This compound is a versatile building block that can be used in research chemicals, as well as reaction components for more complex syntheses.</p>

<p>Cyanodibenzylamine is a synthetic, pharmaceutical preparation. It is an amine that undergoes nucleophilic attack by an amide to form a cyanoguanidine. Cyanodibenzylamine can be used as a stabilizer and additive in pharmaceutical preparations. It also has the ability to bind metal hydroxides, which may be due to the presence of basic fibroblast growth factor and isoquinoline compound. Cyanodibenzylamine is also used as a polymerization initiator in organic chemistry, with hydrocarbon solvents such as benzene or toluene as its solvent.</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>1,4-Diamino-2,3-dicyanoanthraquinone is a chemical compound that belongs to the amines group. It has transcription-polymerase chain activity and inhibits the growth of cancer cells by regulating blood pressure and stimulating the production of growth factors. The effect on cancer cells is due to its ability to inhibit kinases. 1,4-Diamino-2,3-dicyanoanthraquinone has shown an inhibitory effect on glutamate decarboxylase and fatty acid synthase, which are enzymes that regulate cell metabolism. This chemical compound also exhibits quinoline derivatives with a redox potential that can be used as hydrogen chloride in organic synthesis reactions.</p>

<p>2,5-Diaminobenzonitrile is a chemical compound with the molecular formula C6H5N3. It is a white crystalline solid that is insoluble in water and soluble in organic solvents such as acetone, chloroform, and ether. 2,5-Diaminobenzonitrile has been shown to be an effective monomer for polymer synthesis due to its stability and high densities. This chemical also has the ability to undergo hydrogen bonding and form hydrogen peroxide when heated to a temperature of 100 °C. The thermal isomerization of 2,5-diaminobenzonitrile can be slowed by adding other amines or nitrites.</p>

<p>4-Cyanophenylacetic acid is a thiolated organic compound that can act as a framework for the attachment of other functional groups. The synthesis of this compound has been developed in various ways, such as through the use of photoluminescence or coordination chemistry.</p>

<p>4-Amino-3-nitrobenzonitrile is an organic compound that is used as a precursor in the synthesis of drugs to treat infectious diseases. 4-Amino-3-nitrobenzonitrile has been shown to have potent activity against Leishmania species, including L. major and L. braziliensis. It binds to sulfoxides by a nitro group and forms a covalent bond with the sulfoxide. This results in the formation of an intramolecular hydrogen bond between the nitro group and the sulfoxide, which prevents it from forming hydrogen bonds with other molecules. Gel permeation chromatography can be used for analytical determination of this drug. 4-Amino-3-nitrobenzonitrile has also been studied using chemosensors and in vivo studies, showing that it can be used to inhibit protozoa such as Giardia lamblia, Entamoeba histolyt</p>

<p>3,4-Dimethoxybenzylamine is an amine that is used in the synthesis of pharmaceuticals. It can be polymerized by heating with aqueous formaldehyde and hydrochloric acid to form a resin. 3,4-Dimethoxybenzylamine inhibits serotonin receptors, exhibiting inhibitory properties at concentrations of 10-5 M. 3,4-Dimethoxybenzylamine also has pharmacokinetic properties that are similar to vitamin B1. This compound has been shown to inhibit homogeneous catalysts and is used for coatings for ganglion cells.</p>

<p>3-Hydroxyphenylacetonitrile is a molecule that is the precursor for a number of isothiocyanates, which are phytochemicals with antibacterial properties. It has been shown to have inhibitory effects on dopamine hydroxylase, an enzyme that catalyzes the conversion of dopamine to norepinephrine and epinephrine. 3-Hydroxyphenylacetonitrile also inhibits the activity of other active enzymes such as cytochrome P450. The inhibition of these enzymes by 3-hydroxyphenylacetonitrile may be responsible for its antibacterial properties. This molecule is inactivated by cyanides, which leads to its inability to produce any isothiocyanates. Kinetic studies show that 3-hydroxyphenylacetonitrile saturates at high concentrations, leading to decreased production of cyanide.</p>

<p>3-Hydroxybenzylamine hydrochloride (3HBH) is a chemical compound that has been used as a reagent and in the synthesis of other compounds. It is also known to be a useful scaffold for complex compounds, and can be used as a building block for the synthesis of fine chemicals. 3HBH has been found to have many applications in research, such as being an intermediate for pharmaceuticals, pesticides, dyes, and agrochemicals. 3HBH is also useful in organic syntheses where it has been found to react with nitriles and amides to form esters and amides respectively.</p>

<p>7-Cyano-7-deazaguanosine is a nucleoside that belongs to the category of 7-deazapurines. It is an optimized nucleic acid analogue that has been shown to act as a translational inhibitor in vitro and in vivo. This compound has been shown to have high yields in chemical synthesis, which makes it an attractive candidate for optimization and future research. 7-Cyano-7-deazaguanosine is a synthetic nucleotide with anticodon properties, which may be useful for the development of new drugs against bacterial infections.</p>

<p>[(4-Methylphenyl)sulfonyl]acetonitrile is a synthetic compound that has been shown to inhibit the enzyme SHP2. This inhibition leads to decreased proliferation of cells and may be useful in the treatment of degenerative diseases. [(4-Methylphenyl)sulfonyl]acetonitrile is an organic solvent and a nucleophilic reagent that reacts with metal carbonates, such as calcium carbonate, to form carbanions. The carbanion intermediate can react with nucleophiles, such as acetonitrile, to form a new compound that is structurally related to the original starting material.</p>

<p>4-Cyano-4'-aminobiphenyl is a fluorescent dye that exhibits a strong fluorescence under UV irradiation. The dye has an absorption maximum at about 335 nm and a fluorescence emission maximum at about 455 nm, with excitation maxima of 333 nm and 478 nm. It has been used in the development of photocurrent devices, which are used for photochemical reactions and electrochemistry studies. This compound can also be used for the determination of amino groups in organic molecules such as carbostyril. The compound can be synthesized by reacting an amine with an aldehyde in the presence of acid.</p>

<p>The 4-cyanoindole is a fluorescent molecule that binds to proteins and affects protein homeostasis. It has been shown to bind to the sodium salt form of proteins, which are typically found in human liver cells. The binding of 4-cyanoindole to these proteins leads to its reduction by borohydride and fluorescence resonance energy transfer (FRET) between the molecule and the protein. This binding can be detected using a fluorescence lifetime spectroscopy technique, which detects changes in the fluorescence's lifetime as well as intensity. The binding of 4-cyanoindole to proteins has been shown to have anti-cancer properties. It has also been used for detection of monoclonal antibodies against cancer cells or for fluorescent labeling of cancer cells for immunofluorescent microscopy.</p>

<p>7-(Cyanomethoxy)indole is a versatile building block that can be used as a scaffold for the synthesis of complex molecules. It has been used as an intermediate in organic synthesis and as a reaction component for the preparation of useful compounds. 7-(Cyanomethoxy)indole is also known to have high quality and is widely used in research laboratories.</p>

<p>Please enquire for more information about 2-(2-formyl-6-methoxyphenoxy)acetonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>m-Hydroxybenzonitrile is a cationic surfactant that has the ability to form hydrogen bonds with an intramolecular hydrogen. It is used in the production of detergents, textile processing aids, and inks. m-Hydroxybenzonitrile inhibits fatty acids by forming an inhibitory complex at the surface of the cell membrane. This complex disrupts lipid bilayers and inhibits protein synthesis. m-Hydroxybenzonitrile also has been shown to have vibrational properties that can be seen when it absorbs ultraviolet light.</p>

<p>2-Cyanoethyl phosphate barium salt hydrate is an alkaline compound that is soluble in water. It has been used to synthesize phosphodiesters, benzene, dioxan and alcohols. The chemical was originally developed as a reagent for the quantitative conversion of ethyl acetate esters to their corresponding acid chlorides. This reaction can be carried out quantitatively in tetrahydrofuran at room temperature with yields of about 95%. 2-Cyanoethyl phosphate barium salt hydrate also converts alcohols to their corresponding monophosphates quantitatively in alkaline conditions. Crystalline forms are obtained by reacting the compound with triethylamine and benzene.</p>