Cyano-, Nitrile-

<p>2-Cyanobenzamide is a corrosion inhibitor that is used in the electrochemical industry to protect metals from corrosion. It has been shown to be suitable for use as a corrosion inhibitor in salt water and other corrosive environments. 2-Cyanobenzamide has been shown to have light sensitive properties, which is why it should not be exposed to direct light or stored in dark containers. It also inhibits enzymes that are involved in the production of reactive oxygen species (ROS) such as superoxide anion and hydrogen peroxide. The reaction of 2-cyanobenzamide with aluminium, sodium sulfide, and polymeric matrices has also been studied extensively.<br>2-Cyanobenzamide can be synthesized by reacting benzoyl chloride with ammonia and cyanogen bromide. This reaction produces a mixture of mono-, di-, tri-, and tetramers of 2-cyanobenzamide. These products can then be separated using analytical methods such as</p>

<p>4-Bromo-2-cyanoanisole is a synthetic compound that can be used as a ligand in the transition metal catalyzed cross-coupling reaction. This chemical has been shown to form complexes with nickel, palladium, and platinum. 4-Bromo-2-cyanoanisole is also a biomolecule that interacts with other molecules and can be used in the study of natural products.</p>

<p>4-Cyanobenzyl bromide is a chemical compound that is stable in the presence of hydrogen bonds and with a palladium-catalyzed coupling reaction. It has been shown to react with amines to form an azobenzene, which is a fluorescent compound. 4-Cyanobenzyl bromide reacts with x-ray diffraction data and molecular modeling to form halides and hydroxy groups. The mechanism of this reaction is not yet known, but it appears that the initial step involves the formation of a hydrogen bond between the 4-cyanobenzyl group and the amine. Magnetic resonance spectroscopy has confirmed that hippuric acid can be formed from this reaction as well.</p>

<p>2-Phenoxyphenylacetonitrile is a pyrethroid n-oxide that is chemically related to other insecticides that are used in agriculture and against insects such as mosquitoes. 2-Phenoxyphenylacetonitrile is a synthetic compound that has been shown to have an optimum pH of 5.5, which makes it difficult to dissolve in water. The compound's high stability at low pH levels means that it can be used in acidic environments. It also has been shown to have strong activity against human serum and food composition, with no detectable activity against bacteria or fungi.</p>

<p>2-Bromo-4-nitrobenzonitrile is a chemical compound that can be used to study the relationship between genetic polymorphism and chromosome structure. This compound has been found to induce polyploidy in Brassica plants, which may have implications for the evolution of these species. 2-Bromo-4-nitrobenzonitrile also has been shown to be a useful marker for phylogenetic and ecological studies of Lepidium species. The compound is diploid in nature, but can be used as a matrix in tetraploid plants.</p>

<p>3-Cyanocinnamic acid is a reactive, unreactive, and stepwise cycloaddition compound. It can participate in photochemical reactions with other compounds to form photodimers. 3-Cyanocinnamic acid has an optimal reaction temperature of 100°C and a reaction time of 5 minutes. The diradical nature of 3-cyanocinnamic acid makes it sensitive to UV light, and the photochemical reactions are simulated by quantum mechanics calculations. Photodimerisation simulations show that 3-cyanocinnamic acid is capable of forming photodimers with 2-cyanocinnamic acid or 4-cyanocinnamic acid at room temperature.</p>

<p>3-Cyanophenylboronic acid is an organic compound that has been shown to have antimicrobial activity against Pseudomonas aeruginosa. The synthetic pathway of this compound begins with the benzamidine, which reacts with dibutyltin oxide to form 3-cyanophenylboronic acid. This molecule can then be reacted with a cationic polymerization agent such as polyethyleneimine or polyallylamine, producing a polymerized product. When tested in humans, 3-cyanophenylboronic acid showed a high oral bioavailability and low plasma protein binding. It also has a short serum half-life and is metabolized by serine proteases in the liver.</p>

<p>N-(5-Cyano-2-chlorophenyl)acetamide is a high quality, reagent, and versatile building block. It is a fine chemical that can be used as a building block for the synthesis of other compounds. N-(5-Cyano-2-chlorophenyl)acetamide is also a speciality chemical that can be used in research or as a reaction component. It has been found to be useful as an intermediate in the synthesis of complex compounds.<br>END&gt;</p>

<p>2-Acetoxybenzonitrile is an atypical, acidic organic compound with a molecular weight of 136.06 g/mol. It has a melting point of -5.5 °C and decomposes spontaneously at high temperatures to form benzonitrile, carbon dioxide, and water. 2-Acetoxybenzonitrile is able to act as a competitive inhibitor of acetylsalicylic acid (ASA) in the kinetic determination of ASA using acetylation as the rate-determining step. In this experiment, 2-acetoxybenzonitrile was found to be an effective inhibitor of acetylation with a KI value of 1.8 x 10 M. The spectrometer can be used to determine the molecular weight and purity of 2-acetoxybenzonitrile by measuring its absorbance in the ultraviolet region.<br>2-Acetoxybenzonitrile binds metal cations such as Cu(II), Fe(</p>

<p>2-Cyano-3-trifluoromethylpyridine is a fine chemical that is used as a versatile building block in the synthesis of complex compounds. It can be used as an intermediate in research chemicals, reaction components, and speciality chemicals. 2-Cyano-3-trifluoromethylpyridine is a high quality reagent that can be used for the synthesis of various derivatives. It is also a useful scaffold for the development of new drugs and other chemical compounds.</p>

<p>2-Hydroxy-2-(3-phenoxyphenyl)acetonitrile is an organic compound that is synthesized by the reaction of 3-phenoxybenzaldehyde with nitrous acid in aqueous solution. This compound can be racemized by the enzyme lipase and esterified to form an ester linkage. 2-Hydroxy-2-(3-phenoxyphenyl)acetonitrile has been shown to exhibit insecticidal activity against various strains of bacteria, including Bacillus subtilis, Staphylococcus aureus, and Escherichia coli. 2HPA is a pyrethroid insecticide that has been shown to inhibit lipid synthesis by binding to phospholipids in the bacterial cell membrane. This inhibits the production of fatty acids and glycerol phosphate, inhibiting the growth of the bacteria.</p>

<p>Ethyl S-(+)-4-cyano-3-hydroxybutyrate is a chiral molecule that can be used as a catalyst in the transesterification reaction. It acts by binding to the enzyme and immobilizing it on a solid support, which increases its catalytic activity. The hydroxybutanoate is converted into butyric acid, which is produced at high yield using this method. This process of immobilization increases the kinetic rate of the reaction, making it possible for the product to be obtained more quickly.</p>

<p>2-Cyanocinnamic acid is a fatty acid that has been shown to inhibit the synthesis of proteins. It binds to cytochrome c oxidase, inhibiting mitochondrial respiration and electron transport, leading to decreased ATP production. 2-Cyanocinnamic acid is not easily transported out of mitochondria, which leads to its accumulation in the mitochondrial matrix. This accumulation causes synergistic inhibition with glutamate, leading to a decrease in ATP production and an increase in intracellular levels of reactive oxygen species (ROS). The use of 2-cyanoacrylic acid as a mitochondrial transport inhibitor has been proposed for the treatment of obesity and diabetes.<br>2-Cyanocinnamic acid also inhibits fatty acid uptake by binding to the protein translocase at the outer membrane of cells. This binding prevents monomers from entering the cell, where they are broken down by beta oxidation and converted into acetyl-CoA, which can be used for energy production or stored as triglycer</p>

<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>

<p>4-Cyano-2-fluorobenzyl alcohol is a reagent that is used to produce chlorine and hydrochloric acid. It is also used industrially in the production of potassium chloride, a compound that is used in fertilizers, animal feed supplements, and water treatment. 4-Cyano-2-fluorobenzyl alcohol reacts with chloride ions to form hypochlorous acid (HOCl), which then reacts with water to form hydrogen chloride gas. The reaction with fluoride ions leads to the formation of hydrofluoric acid (HF).</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>4-mercaptobenzonitrile (4MBN) is a typical compound used in many spectroscopic experiments. The addition of 4-mercaptobenzonitrile to metal surfaces is used to create self-assembled monolayers with metals. For numerous reasons, it can difficult to immbolize certain chemical groups on surfaces. The addition of 4-mercaptobenzonitrile forms a modified metal surface that enhances technique sensitivity and serves as tool for a better understanding of the interfaces. In recent years, the use of 4-mercaptobenzonitrile together with other molecules on metal nanoparticles has been explored for biomedicinal purposes, serving as a tool for creating surface-enhanced Raman scattering tags (SER tags), useful as cancer biomarker imaging (Li, 2018).</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>32-Carboxycyanocobalamin is a fine chemical that is used in the synthesis of complex compounds. It is a versatile building block, which can be used in reactions to synthesize other compounds and as a scaffold for drug discovery. 32-Carboxycyanocobalamin is also a reagent that has been used in organic chemistry and analytical chemistry. CAS No. 121483-62-3</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>