Cyano-, Nitrile-

<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>

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<p>4-Cyano-2-fluorobenzoic acid methyl ester is a versatile building block for complex compounds. It can be used as a reagent to synthesize other compounds and as a speciality chemical with high quality. This chemical is also an intermediate in the synthesis of other compounds, such as 4-cyano-2-fluorobenzoic acid ethyl ester, which has been shown to be useful in the synthesis of β-lactam antibiotics.</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>

<p>3-Cyano-5-bromopyridine is an enantiopure organic compound that belongs to the group of halides. It is a functional group that is a reagent in organic synthesis, and it can be used as a precursor to dyestuffs. 3-Cyano-5-bromopyridine has been shown to have antimicrobial activity against bacteria and fungi. It also has a metabotropic glutamate receptor subtype selective affinity, which may be due to its ability to bind with glutamate in complex molecules.</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>Azobis(4-cyanovaleric acid) is a chemical compound that has reactive functional groups. It is a particle that is soluble in acetate extract and hydrochloric acid. The synthesis of Azobis(4-cyanovaleric acid) involves the reaction of 4-cyanoacrylic acid with 2,2'-azobis(2-methylpropionitrile). It is used as an intermediate in the preparation of polymers. Azobis(4-cyanovaleric acid) is used for the treatment of infectious diseases such as tuberculosis and malaria. The production of chain reactions with other molecules makes this chemical reactive and unstable. Azobis(4-cyanovaleric acid) also reacts with nucleophilic groups, such as hydroxyl groups, to form a covalent bond. This process can be reversed by adding a strong base or oxidant.</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>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>3,5-Dibromo-4-methoxybenzonitrile (DBMB) is a pentane that can be synthesized in the laboratory. DBMB is used as a weed control agent to kill weeds and grasses in neoprene rubber products and other materials. The chemical reacts with nitro groups on the surface of the material, producing an unstable intermediate that decomposes into pentane and nitric acid. 3,5-Dibromo-4-methoxybenzonitrile has been shown to have low toxicity to mammals at high doses.<br>The compound may also be used as a chemical intermediate for the synthesis of other compounds or drugs. Nitro groups may be reduced by reductants such as sodium borohydride or lithium aluminium hydride to produce analdehyde derivatives.</p>

<p>3-Cyanobenzylamine HCl is a high quality chemical that is used as a reagent, intermediate, or building block in the synthesis of complex compounds. It is a fine chemical and speciality chemical that may be used as a research chemical and versatile building block for the synthesis of organic compounds. 3-Cyanobenzylamine HCl has been shown to react with other chemicals to form useful scaffolds and building blocks, such as amides, amino acid esters, and ureas.</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>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>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>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>Substrate of benzylamine oxidase and monoamine oxidase B</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-Acetylbenzonitrile is an isomeric, asymmetric synthesis that has been synthesised in the presence of copper complex and salicylic acid. The reaction was carried out with a gaseous phase, where the chalcone was formed. The experimental techniques used were cross-coupling reactions and molecular modeling techniques. 3-Acetylbenzonitrile has been synthesised by a rationalized enthalpic approach that includes alcohol dehydrogenases and molecular modeling techniques.</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>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>Ethyl 3-cyanopropanoate is an organic compound with the formula CH3C(O)CH2CN. It is a colorless liquid that boils at 100 °C. It is used in the synthesis of other organic compounds, such as oxazolidinones, cyclopropenes, and quinolizines. The yield can be increased to 98% by using a catalyst such as potassium tert-butoxide or zinc chloride in the reaction. The reaction proceeds through an elimination followed by an acid-catalyzed alkylation to afford the desired product. This process also results in a high yield of ethyl bromoacetate as a side product.</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>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>

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<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>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-Chloro-5-cyanopyrazine is a synthetic compound that has been shown to have anti-cancer properties. It is an acceptor molecule that has a nucleophilic character and can react with electrophiles to form covalent bonds. This compound has been shown to selectively inhibit the growth of cancer cells in vitro. The mechanism of action is not yet clear, but it may be due to its ability to induce apoptosis and arrest cell cycle progression at the G1 phase. 2-Chloro-5-cyanopyrazine also has the potential for use as an analytical reagent because of its high solubility in organic solvents. In addition, this compound can be used as a copper donor in reactions involving carboxylic acids or other nucleophiles. <br>2-Chloro-5-cyanopyrazine can be synthesized from benzene and chloropicrin in the presence of copper(II)</p>

<p>2-Chloro-5-hydroxybenzonitrile is a versatile, building block chemical that can be used as a reactant or intermediate in the synthesis of other compounds. It is also an excellent research chemical with a high quality and purity. 2-Chloro-5-hydroxybenzonitrile has many uses, such as being a reagent for organic synthesis, a speciality chemical, and a useful intermediate. This compound is suitable for complex synthesis and has been shown to be useful as a building block or scaffold in the production of other chemicals.</p>

<p>3-Amino-4-methylbenzonitrile is an organic compound that is produced by the oxidative dehydrogenation of 3,4-dimethylaniline. It has been shown to undergo a number of reactions, including hydrochloric acid transfer hydrogenation and diazotization. This reaction yields 3-amino-4-methylbenzonitrile, dimethylamine and anilines. The transfer hydrogenation of nitroarenes with 3-amino-4-methylbenzonitrile gives 3-(3,4)-diaminobenzonitrile and 2,6-dinitrotoluene. The optimization of this reaction has led to the discovery of new nitrite derivatives as a result of the addition of nitrite in the presence of 3-amino-4-methylbenzonitrile.</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>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>2-Cyanoacetamide is an organic compound that is used in pharmaceutical preparations. It reacts with malonic acid to form a dioxime, which is a precursor of various drugs. The optimum concentration for the reaction to occur is at 10% (w/v). The reaction mechanism has not been fully elucidated and it involves the transfer of nitrogen from an amide group to a carbonyl group. 2-Cyanoacetamide has shown anti-angiogenic effects in mice by inhibiting the expression of Mcl-1 protein, which is involved in the regulation of apoptosis and inflammation. This drug also has biological functions as a precursor for dopamine, which helps regulate motor and cognitive functions.</p>

<p>5-Cyano-DL-tryptophan is an antimicrobial peptide that exhibits potent antimicrobial activity against Gram-positive and Gram-negative bacteria. It also has a high affinity for the bacterial ribosome, which leads to inhibition of protein synthesis. 5-Cyano-DL-tryptophan can be synthesized by dehydration of tryptophan in a model system. The molecule is an analog of the natural amino acid tryptophan and has fluorescence properties that are sensitive to hydration levels. 5-Cyano-DL-tryptophan binds to the peptide binding site on the ribosome and induces a frequency shift in its fluorescence emission spectrum when bound. This property makes it a useful tool for studying peptide binding sites on the ribosome.</p>

<p>2-Amino-4-cyano-phenol is a compound that has been shown to have antitubercular activity. It modulates the activity of cromakalim, which is a drug used for the treatment of tuberculosis. 2-Amino-4-cyano-phenol is also an antibacterial agent and has been shown to activate bacterial DNA replication and protein synthesis. The mechanism of action of this compound is thought to be due in part to its ability to bind with the ribosomes on the outside surface of cells and inhibit their function. 2-Amino-4-cyano-phenol has also been shown to have structural similarities with phenylephrine, which inhibits bacterial growth by binding to DNA gyrase, thereby preventing transcription and replication.</p>

<p>2,5-Dimethoxybenzonitrile is a polymerized organic compound that belongs to the class of benzene compounds. It is a monomer with two methyl groups on either side of the benzene ring. 2,5-Dimethoxybenzonitrile has been studied in terms of its transition and optimization properties using techniques such as IR and NMR spectroscopy. The frequencies of the chemical bonds have been analyzed, and it has been found that the molecule is centrosymmetric. 2,5-Dimethoxybenzonitrile can also be used to form polymers with other molecules by linking them together through covalent bonds.</p>

<p>4-Hydroxyphenylacetonitrile (HPA) is a chemical compound that belongs to the group of nitriles. It is a precursor to the pigment sinalbin, which is found in corynebacterium and related bacteria. HPA has been shown to have an apoptotic effect on human cells, which may be due to its ability to inhibit protein synthesis and induce DNA fragmentation. The synthetic pathway for HPA starts with the conversion of L-phenylalanine into 4-hydroxyphenylpyruvic acid by a wild-type strain or bacterial strain. The 4-hydroxyphenylpyruvic acid is then converted into 4-hydroxybenzaldehyde through polymerase chain reactions or expression plasmids in corynebacterium glutamicum. This molecule can then be transformed into HPA by hydrolysis with hydrochloric acid or enzymatic activity. HPA has also been shown to stimulate</p>

<p>3-Cyanophenylacetic acid is a versatile building block and useful intermediate that can be used in the synthesis of a wide range of organic compounds. 3-Cyanophenylacetic acid is a fine chemical with CAS No. 1878-71-3 that can be used as a research chemical, reaction component, or speciality chemical. It is an important reagent for making complex organic compounds. 3-Cyanophenylacetic acid is a high quality product with the following characteristics: <br>1) Colorless crystals; <br>2) Soluble in water; <br>3) Soluble in acetone; <br>4) Slightly soluble in ether; <br>5) Reactivity: stable to heat, light, and air; <br>6) pH (1% solution): 2.0 - 4.0; <br>7) Melting point: 129 °C; <br>8) Boiling point: 188 °C at 760 mmH</p>

<p>5-Cyano-2-fluorobenzoic acid is a macrocyclization agent that is used in the synthesis of 16-membered macrocycles. It is a nucleophilic reagent that reacts with an electrophile to form a 5,5'-bifluoro-2,2'-dioxodibenzofuranone. This reaction can be performed under mild conditions and proceeds via a 1,4-addition mechanism. The product has two stereogenic centers and four stereoisomers that are formed by the relative configuration of these centers. 5-Cyano-2-fluorobenzoic acid also has application in the clinic as an analogue for fluoroquinolones.</p>

<p>Pyridine-3-acetonitrile is a coordination complex that can be used for the treatment of diabetes. It has been shown to have a high affinity for plasma glucose and to be selective for biological samples containing amino acids, such as proteins. The molecule is able to bind with carbon disulphide in order to form the active methylene, which has been shown to be an effective bifunctional ligand. The compound has also been shown to have a ph optimum of 9.8 - 10.2 and exhibits an atomic orbital with a molecular electrostatic potential of 0.5 eV. Pyridine-3-acetonitrile binds strongly to nucleophilic groups, such as amines and hydroxyls, making it suitable for use as a ligand in metal complexes. This compound may also have some interesting properties related to its morphology, which can be further investigated using functional theory and molecular electrostatic potential.br&gt;br&gt; br&gt;br&gt;</p>

<p>2-Hydroxy-4-nitrobenzonitrile is a nitrile derivative that has an antibacterial activity. This compound interacts with the pyochelin, a siderophore in Pseudomonas aeruginosa. The antibiotic inhibits the uptake of pyochelin by the bacteria and causes cell death by inhibiting the synthesis of proteins necessary for bacterial growth. 2-Hydroxy-4-nitrobenzonitrile can be used as a potential stabilizer for materials such as polystyrene and polyurethane which are susceptible to degradation by hydrolysis or oxidation. In addition, this compound is also useful in gram-negative bacterium due to its ability to inhibit their growth by binding to their ribosomes. The conformational studies have been shown to be important for understanding the biological properties of this molecule.</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>

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<p>1-Cyano-4-(dimethylamino)pyridinium tetrafluoroborate (CDAP) is an organic cyanylating agent.  It is reactive under acidic conditions giving CDAP an advantage over other sulfhydryl labeling agents, as it can avoid potential thiol-disulfide exchange.</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>

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<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>2-Cyano-5-fluorobenzoic acid ethyl ester is a chemical compound with the formula C6H4(COOCH2)2FO. The compound is an intermediate in the synthesis of other chemicals, such as pharmaceuticals. It is also used as a building block in other syntheses. 2-Cyano-5-fluorobenzoic acid ethyl ester has been assigned CAS No. 1260751-65-2 and is useful in organic synthesis because it is a versatile building block, complex compound, and fine chemical.</p>

<p>4-Nitrobenzylamine hydrochloride is a bifunctional immobilizing agent that can be used for the immobilization of Zn2+. It reacts with nitrogen atoms, forming an amination reaction. The linker is covalently immobilized to the surface and the nature of this chemical is synthetic. 4-Nitrobenzylamine hydrochloride is synthesized by reacting nitric acid with benzaldehyde in ammonia solution at room temperature. This chemical has shown to be effective in reactions where a flow rate is needed or when diamidines are present in the reaction mixture.</p>

<p>4-Bromo-3-cyanopyridine is a reactive chemical that can be used as a building block in organic synthesis. It is often used as a starting material for the synthesis of heterocycles and other complex compounds. 4-Bromo-3-cyanopyridine is a versatile reagent with high quality and can be used in research, pharmaceuticals, agrochemicals, or industrial chemicals. CAS No. 154237-70-4.</p>

<p>Ethyl acetamidocyanoacetate is an amide which inhibits the enzyme thrombin. It inhibits the conversion of fibrinogen to fibrin, and thus prevents blood clot formation. Ethyl acetamidocyanoacetate has been shown to inhibit serine protease, one of the most abundant enzymes in the human body. This inhibition causes a decrease in inflammatory diseases caused by these enzymes. Ethyl acetamidocyanoacetate also has analog properties that can be used for solid-phase synthesis.</p>