Cyano-, Nitrile-

<p>4-Ethoxybenzonitrile is an organic compound that belongs to the group of nitroalkanes. It is a substrate for reductive amination, which is a reaction in which the nitro group on 4-ethoxybenzonitrile is reduced by an amine to form an amide. This reaction can be facilitated by metal catalysts, such as copper(II) acetate and zinc chloride. The reaction yields high selectivity (&gt;90%) with respect to the product formed and has been shown to be more efficient than other reductive amination reactions. 4-Ethoxybenzonitrile has been used as a building block for various compounds, including dyestuffs, pharmaceuticals, and pesticides. 4-Ethoxybenzonitrile is also resistant to tyrosinase due to its lack of electron donating groups on its aromatic ring.</p>

<p>4-(4-Fluorophenoxy)benzylamine hydrochloride is a metabolic agent that inhibits the metabolism of phenylpropionic acid and butanoic acid. It is used industrially as an oxime to protect other organic compounds from damage by peroxides, such as in polymerization reactions. 4-(4-Fluorophenoxy)benzylamine hydrochloride has been shown to be effective in treating metabolic diseases, such as phenylketonuria and urea cycle disorders.</p>

<p>3,4-Dihydroxybenzonitrile is a chemical compound that is found in soybean lipoxygenase. The molecule has been shown to be an excellent Michaelis-Menten substrate and hydrogen bonding partner. It also reacts with chlorine to form chlorinating agents such as 3,4-dichlorobenzonitrile and 3,4-dibromobenzonitrile. 3,4-Dihydroxybenzonitrile can act as a nucleophile and forms stable complexes when reacted with hydroxyl group compounds such as protocatechuic acid or reaction solution. This chemical is reactive and can be activated by redox cycling or light.<br>3,4-Dihydroxybenzonitrile has been used to treat protocatechuic acid levels in the blood of patients with chronic liver disease who are being treated for alcoholism.</p>

<p>2-Bromo-6-fluorobenzonitrile is an organic compound with a molecular formula of C6H3BrF. It is a colorless liquid that is used as a precursor in the synthesis of other compounds. 2-Bromo-6-fluorobenzonitrile has been shown to be an efficient fluorophore and can be activated by electron transfer, thermally, or chemically. 2-Bromo-6-fluorobenzonitrile also has a quantum efficiency of 0.5% and transport properties that make it ideal for fluorescence microscopy. The fluorescence intensity of 2-bromo-6-fluorobenzonitrile is proportional to the amount of energy absorbed, which makes it useful for quantifying the concentration of fluorescent molecules in solution. 2-Bromo-6-fluorobenzonitrile has also been shown to have high quantum yields and high efficiency levels when</p>

<p>4-Cyanobiphenyl is a contaminant of the environment. It is a reactive substance that can be found in the air, soil, and water. 4-Cyanobiphenyl is an active substance that can be used as an intermediate for the production of other chemicals. The chemical structure of 4-cyanobiphenyl has been elucidated by using a number of spectroscopic techniques including Raman spectroscopy. 4-Cyanobiphenyl is unstable in acidic conditions and reacts with chloride ions to form crotonic acid and benzoate. This reaction also occurs under basic conditions with biphenyl to form benzoate and low energy products such as benzene or phenol.</p>

<p>3-(Cyanomethyl)benzoic acid is a useful building block that is used as a reagent in the production of pharmaceuticals and research chemicals. It is also used as a speciality chemical and as a high-quality fine chemical. This compound has versatile uses, including reactions with other chemicals to form complex compounds, and can be used as a reaction component or an intermediate in the synthesis of other chemicals. 3-(Cyanomethyl)benzoic acid has no known toxicity and its CAS number is 5689-33-8.</p>

<p>4-Amino-3-nitrobenzylamine hydrochloride is a potential vanilloid receptor antagonist with potent antagonistic activities. It has been shown to inhibit the activation of neuronal TRPV1 receptors, as well as the uptake of 4-aminobenzoic acid (4-BA) in rat brain synaptosomes. In addition, this compound can be used to optimize drug structure, acting as an amide and alkyl groups. 4-Amino-3-nitrobenzylamine hydrochloride binds to the vanilloid receptor TRPV1 and blocks its activation. This prevents the release of proinflammatory substances that are responsible for pain, inflammation, and tissue injury.</p>

<p>Diphenylacetonitrile is an organic compound that has a low energy and is used as a nutritional supplement. It is a derivative of mandelonitrile, which can be synthesized by the Friedel-Crafts reaction between chloroform and diphenylacetic acid. Diphenylacetonitrile is an aromatic hydrocarbon with nitrogen atoms and hydroxyl groups, which can be found in the virus or p. aeruginosa. The molecule has been shown to have anti-inflammatory potency in animal models. The synthesis of this compound involves the use of halides, such as hydrogen sulfate or bromide, which are also present in high concentrations in this product. <br>Diphenylacetonitrile (DPCN) is a low-energy nitrile that undergoes Friedel-Crafts reactions with chloroform to produce the corresponding chloride (DPCCl). DPCN has been shown to inhibit inflammatory responses</p>

<p>(2,3-Dichlorophenyl)acetonitrile is a fine chemical that is useful as a building block in the synthesis of more complex compounds. It has been used in research as a reagent and as a speciality chemical. (2,3-Dichlorophenyl)acetonitrile reacts with many different types of compounds to form new molecules. This intermediate can be used in the synthesis of many different types of compounds and also serves as an important scaffold for larger molecules.</p>

<p>2-Fluoro-4-methoxybenzylamine hydrochloride is a potent inhibitor of polymerase (DNA and RNA). It has been shown to inhibit the growth of human breast cancer cells and to induce apoptosis. 2-Fluoro-4-methoxybenzylamine hydrochloride binds to the polymerase, which blocks synthesis of DNA or RNA. The binding site is located near the active site of the enzyme. This drug also has an insulin-like effect by stimulating IGF-I production and increasing protein synthesis in somatotrophic cells.</p>

<p>3-Aminobenzonitrile is an amine that has been shown to inhibit the growth of bacteria. It was synthesized by the reaction of nitrobenzene with benzamide in the presence of acetic acid. The chemical structure of 3-aminobenzonitrile is similar to that of a group of natural amino acids, including cysteine and tryptophan, which are known inhibitors of bacterial growth. This compound is soluble in organic solvents and can be used as an injection solution. 3-Aminobenzonitrile has been evaluated by kinetic studies and found to have a high affinity for bacterial cells, with an inhibition constant (Ki) value of 0.37 mM. It is also active against other microorganisms such as yeast or mold fungi, but not against plant or animal cells. 3-Aminobenzonitrile inhibits the synthesis of proteins by binding to a number of different sites on the ribosomes where</p>

<p>Ethyl 4-cyano-3-nitrobenzoate is a chemical compound with the structural formula of CHNO. It is a building block for organic synthesis and can be used in the production of high quality research chemicals and speciality chemicals. Ethyl 4-cyano-3-nitrobenzoate has been shown to react with a variety of amines to form urea derivatives that are useful as versatile building blocks or complex compounds. This reagent is also useful as an intermediate in the synthesis of various pharmaceuticals. CAS No. 321162-58-7</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-Bromo-5-cyanonitrobenzene is a chemical compound that has been shown to have broad-spectrum activity against drug-resistant bacteria. It is able to kill gram-negative and gram-positive bacteria, including drug-resistant strains. The mechanism of action for 2-bromo-5-cyanonitrobenzene is not well understood but it has been observed that the molecule undergoes an oxidative cyclization reaction in the presence of chloride ions or hydroxides. This process leads to the formation of a nitrosobenzene metabolite which reacts with DNA to inhibit protein synthesis and cause cell death. 2-Bromo-5-cyanonitrobenzene has also been shown to be potent against a wide range of different types of bacteria, including those most commonly associated with skin infections, respiratory tract infections, and urinary tract infections.</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>Please enquire for more information about 2-(6-Benzyloxyindolyl)acetonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<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>3-Cyano-4-methoxybenzoic acid is a white crystalline solid that is soluble in water. This compound is a useful intermediate for the synthesis of other organic compounds, as well as a useful scaffold for the synthesis of complex compounds. 3-Cyano-4-methoxybenzoic acid also has potential use as a research chemical, and can be used as an effective building block for the preparation of fine chemicals.<br>3-Cyano-4-methoxybenzoic acid may be used to produce speciality chemicals such as pharmaceuticals, dyes, pesticides, and perfumes. It can also be used to synthesize compounds with diverse functionalities.</p>

<p>1-Isocyanoadamantane is a compound that exhibits anti-influenza drug activity. It has been shown to inhibit virus replication by interacting with the active site of the influenza virus ribonucleoprotein (RNP) and inhibiting the synthesis of viral proteins. 1-Isocyanoadamantane binds to the RNP through coordination chemistry, which is mediated by nitrogen atoms on the amides and amines in its structure. The reaction mechanism for 1-isocyanoadamantane consists of two steps: reductive elimination followed by functional group activation. In this process, an amide or an amine is eliminated as a hydrogen atom, while a functional group reacts with it to form a new bond.</p>

<p>Cyanomethyl)urea is a fine chemical that belongs to a class of compounds known as ureas. It is used as a versatile building block in the synthesis of more complex compounds, as a research chemical and as an intermediate. It can be used to synthesize pharmaceuticals, pesticides, and other chemicals. Cyanomethyl)urea is used in the production of polyurethane foams, which are commonly found in mattresses, furniture upholstery and insulation.</p>