Cyano-, Nitrile-

<p>4-Fluorobenzylamine is a chemical compound with the molecular formula CHF. It has been shown to radiosensitize tumor cells by inhibiting the synthesis of cyclin D2, which is required for cell proliferation. 4-Fluorobenzylamine can also be used in asymmetric synthesis reactions such as nitration and trifluoroacetic acid hydrolysis. 4-Fluorobenzylamine has been shown to have synergistic effects on cells when paired with flupirtine or maleate. This synergistic effect is primarily due to its ability to inhibit DNA repair, which leads to cell death through apoptosis or necrosis.</p>

<p>Xylene cyanol is a chemical compound that belongs to the group of phenols. It has been shown to be active in vitro against human skin cancer cells, and induces cell lysis. Xylene cyanol has also been found to bind to the BCR-ABL kinase domain, which is an enzyme that plays a crucial role in the development of leukemia and other autoimmune diseases. Xylene cyanol binds to dna binding domains on the protein surface and forms an adduct with bcr-abl kinase, which inhibits its activity. This inhibition prevents activation of this enzyme and leads to cell death by preventing DNA synthesis.</p>

<p>1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 3-(2-cyanoethyl) 5-methyl ester is a chemical compound that has the CAS number 75130-24-4. It is a white powder with a melting point of 144°C. This chemical is soluble in acetone, ether and chloroform. It can be used as a building block for organic synthesis due to its versatility and useful scaffold.</p>

<p>3-Cyanobenzamide is an organic compound with the formula CHC(N)NH. It is a white crystalline solid that can be obtained by reacting benzamide with cyanoacetylene. There are three possible isomers of 3-cyanobenzamide: 3-cyano-1-(substituted phenyl)benzamide, 3-cyano-2-(substituted phenyl)benzamide, and 3-cyano-3-(substituted phenyl)benzamide. The optimal reaction conditions for the synthesis of 3-cyanobenzamide are in the presence of hydrogen bonding, such as n-hexane, amide, and phase equilibrium. Studies have determined that 3-cyanobenzamide has the potential to cause cancer or liver toxicity in humans. In addition, this chemical has been shown to be an effective inhibitor of alpha glucosidase enzymes in vitro and in vivo.</p>

<p>tert-Butyl 4-cyanobenzylcarbamate (tB4Cbz) is a high quality chemical that can be used as a reagent, complex compound, or useful intermediate in the production of fine chemicals. Tert-Butyl 4-cyanobenzylcarbamate is also a useful scaffold for the synthesis of speciality chemicals and research chemicals. It can be used as a versatile building block for reactions involving amides, nitriles, esters, and amines.</p>

<p>4-Cyanoheptane is a liquid that has been decarboxylated, which means it contains no CO2 molecules. It is an organic solvent with a boiling point of -2°C and a density of 0.7 g/mL. This product is used in the hydrolysis of carboxylic acids to form carboxylates. 4-Cyanoheptane has been shown to be able to hydrolyze amides, carbones, phenoxy groups, and functional groups as well as produce alkylation reactions with high concentrations.</p>

<p>Please enquire for more information about Ethyl (2Z)-2-cyano-3-(2-furyl)acrylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromo-5-chlorophenylacetonitrile is an organic compound that is used as a reagent and building block in the synthesis of other chemicals. It is a colourless liquid that can be used to synthesize complex compounds. 2-Bromo-5-chlorophenylacetonitrile has been shown to be useful in the synthesis of pharmaceuticals, pesticides, and herbicides. This chemical can be used as a versatile intermediate or building block for the production of high quality research chemicals and specialty chemicals. 2-Bromo-5-chlorophenylacetonitrile is not on the list of chemical substances classified as hazardous according to EU regulation (EINECS) No. 231-1003.</p>

<p>1,2-Diphenyl-1-cyanoethylene is a molecule that is involved in the cancer process. It has been shown to inhibit the growth of skin cancer cells and other types of cancer cells by binding to mitochondria and inhibiting the formation of proton gradients across mitochondrial membranes. This inhibition leads to a decrease in cellular ATP production and an increase in reactive oxygen species (ROS), resulting in cell death. 1,2-Diphenyl-1-cyanoethylene also has anticancer activity due to its ability to induce light emission from the skin and interfere with the optical properties of holothuria, which are sea cucumbers.</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>2-Hydroxy-3-methylbenzonitrile is a high quality chemical that is used as an intermediate in the synthesis of complex compounds. It can be used as a reagent in organic chemistry, and has been shown to be useful for the production of fine chemicals, such as antibiotics. 2-Hydroxy-3-methylbenzonitrile is also a versatile building block for the production of pharmaceuticals and research chemicals. It can be used as a reaction component for the synthesis of speciality chemicals and various building blocks.</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>2,5-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-Octylbenzylamine is a hydrophobic molecule that is soluble in organic solvents. In simulations, it was shown to have affinity for anions and aromatic hydrocarbons, as well as the ability to be immobilized on surfaces. 4-Octylbenzylamine is also a chromatographic stationary phase that can be used to separate solutes with similar properties. This molecule has been oriented so that it binds to the hydrated surface of the column, which improves its affinity for anions and aromatic hydrocarbons. The high-performance liquid chromatography (HPLC) technique utilizes this property to separate molecules of different affinities from one another in a systematic manner.</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>5-Acetyl-2-aminobenzonitrile is a versatile building block that can be used as an intermediate in the synthesis of a wide range of chemicals. It has been used to produce pharmaceuticals and other useful compounds, including research chemicals and speciality chemicals. 5-Acetyl-2-aminobenzonitrile is also a useful reagent for the production of organic products. The compound is available at high purity levels.</p>

<p>4-Cyanocinnamic acid is a fatty acid that has been shown to be a substrate for the bacterial enzyme cinnamate 4-hydroxylase. The molecular weight of this compound is 136.16 g/mol, and it has a constant boiling point of 206°C. It can be synthesized from phenylacetic acid and p-coumaric acid using a transesterification reaction. This compound is reactive with carbonyl groups, which makes it useful in the detection of gram-positive bacteria by fluorescent probes or fluorescent dyes. 4-Cyanocinnamic acid is unreactive with esters of carboxylic acids, such as methyl esters, making it useful for the determination of fatty acids in isolates.</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>Mesitylacetonitrile is a mesityl-substituted acetonitrile. It is used in organic synthesis as a Grignard reagent, which is an organometallic compound containing an alkyl or other carbon group bound to magnesium. Mesitylacetonitrile has been shown to react with chlorides to produce furyl chlorides and chloride. Mesitylacetonitrile can be synthesized by reacting phenylacetonitrile (a byproduct of the synthesis of acetone) with chlorine gas and hydrogen in the presence of a catalyst such as copper(II) chloride. This reaction produces mesitylacetonitrile and hydrogen chloride gas as byproducts. The compound has been used to synthesize corticotropin-releasing factor receptor antagonists that have potential therapeutic applications for the treatment of stress-related disorders.</p>