Cyano-, Nitrile-

<p>3,4-Dinitrobenzonitrile is a fine chemical that is used as a versatile building block in the synthesis of complex organic compounds. It is also used as a research chemical and a reaction component in organic synthesis. 3,4-Dinitrobenzonitrile is stable against oxidation and hydrolysis, making it an ideal intermediate for other reactions. CAS No. 4248-33-3</p>

<p>(2-Methoxyphenoxy)acetonitrile is a versatile building block that has been used in the synthesis of fine chemicals, complex compounds, research chemicals, reagents and speciality chemicals. It is a useful building block for high quality pharmaceuticals. (2-Methoxyphenoxy)acetonitrile can be used as a reaction component or scaffold to synthesize organic molecules with interesting biological activities.</p>

<p>2-Cyano-3-fluoro-4-bromo aniline is a plant growth regulator that can be used to prevent and control the spread of viral diseases in plants. 2-Cyano-3-fluoro-4-bromo aniline inhibits the replication of influenza virus strains by binding to the viral coat protein. It also has been shown to inhibit proteolytic enzymes when applied as a coating on particles. The main mechanism of this compound is through its ability to bind to regulatory proteins, which prevents them from binding with other regulatory proteins and activating transcription factors. The expression profile suggests that this compound may regulate the expression of genes involved in plant development, cell division, and response to stress.</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>4-Cyanobenzoic acid ethyl ester is a hydrogen-bonding acceptor that is also able to form exciplexes with styrene. It has a conformation that is similar to that of aminobenzoate, which is a hydrogen-bonding donor. 4-Cyanobenzoic acid ethyl ester reacts with solvents such as benzene and chloroform, undergoing hydration reactions to form the corresponding 4-cyanophenol derivatives. It undergoes cyclization when heated in the presence of ruthenium(II) chloride to produce 1,4-dihydropyridine derivatives. The reaction mechanism for this reaction consists of two steps: an intramolecular nucleophilic attack followed by an intramolecular electrophilic substitution. The deionized water used in this synthetic process eliminates the need for drying agents and stabilizers, making it easier to carry out the synthesis.</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>

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

<p>2,4-Dimethoxybenzylamine hydrochloride is a substrate for glutathione reductase and a competitive inhibitor of dithioerythritol. The reaction mechanism is the same as that of triflic acid, which is generated by the reaction between triflic acid and glutathione. The inhibitory effect of 2,4-dimethoxybenzylamine hydrochloride on glutathione reductase has been studied computationally using molecular docking simulations. It was found that 2,4-dimethoxybenzylamine hydrochloride binds to the active site of glutathione reductase with an affinity comparable to that of triflic acid. This computational study also revealed that 2,4-dimethoxybenzylamine hydrochloride can be converted into triflic acid in vivo.</p>

<p>4-Amino-2-bromobenzonitrile is a crystallized ligand with a molecular formula of C6H7BrN. It belongs to the cationic class of ligands and has been shown to form intermolecular hydrogen bonds with aromatic rings. The crystal has a hexagonal unit cell and space group P-1. 4-Amino-2-bromobenzonitrile has been used as an elemental analysis reagent in the determination of copper, lead, zinc, and cadmium.</p>

<p>2-Bromo-4-cyanotoluene is a ligand that is used in cross-coupling reactions. It is used to form complexes with metals, such as palladium and nickel, for the preparation of organometallic reagents. 2-Bromo-4-cyanotoluene has been shown to inhibit secretory phospholipase A2 (sPLA2) and PLA2 activity in a fluorimetric assay. This compound also inhibits the catalytic activity of spla2, which is an enzyme involved in the biosynthesis of arachidonic acid. 2-Bromo-4-cyanotoluene also inhibits piperazine synthesis by reacting with the nitrogen atom on the piperazine ring.</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>

<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>Lobetyolin is a phenolic compound that has been found to be an inhibitor of monoamine oxidase. Lobetyolin is an acetylated derivative of 4-hydroxy-3-methoxyphenylacetonitrile. It has been shown to inhibit bacterial growth in vitro, with the exception of Mycobacterium tuberculosis and Mycobacterium avium complex. The optimal reaction time for lobetyolin is 3 hours at a pH between 7 and 8, with a yield of 66% at room temperature. Lobetyolin reacts rapidly with amines, alkylating them as it undergoes oxidation by hydrogen peroxide. Lobetyolin also reacts slowly with dopamine and aldehydes, but more readily with chlorides, yielding lobetyrine and chloroacetaldehyde respectively.</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>

4-Bromo-3-cyanotoluene is a quinazolinone that can be synthesized by reacting 2-bromotoluene with nitric acid. It is a substrate for the synthesis of other quinazolinones.

<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>

3-Cyano-4-methylnitrobenzene is a nitro compound that can be prepared by the reaction of nitric acid with aniline. It has been shown to have a strong affinity for oxygen, which may be due to its pyran ring. 3-Cyano-4-methylnitrobenzene has been found to react with acetonitrile in an electrochemical experiment, leading to the formation of nitronium ion and nitrate ion. The mechanism for this reaction is not well understood, but it offers a convenient way of preparing 3-cyano-4-methylnitrobenzene from nitric acid and aniline.

<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>

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.

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.