Cyano-, Nitrile-

<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-Methoxyphenylacetonitrile (3MPAN) is a small molecule that has been shown to inhibit the activity of kinases, which are enzymes that transfer phosphate groups from ATP onto other substrates. 3MPAN has been found to be selective for the estrogen receptor alpha (ERα), with little or no effect on ERβ, and shows promise as a potential drug for hormone-dependent breast cancer. It also inhibits fatty acid synthesis and is active against some viruses. 3MPAN binds to the enzyme's ATP binding site and blocks phosphorylation by preventing access of ATP. This prevents DNA synthesis and protein synthesis, leading to cell death.</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>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>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>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>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>5,6-Diamino-2,3-dicyanopyrazine (5,6-DDA) is a synthetic compound that has been shown to emit in the visible region. The emission spectrum of 5,6-DDA shows three peaks at 599 nm, 614 nm, and 637 nm. The molecular orbitals of 5,6-DDA are calculated to be sp2 hybridized with a singlet ground state. This molecule has been shown to form imines with aniline and pyrrole in the presence of chloride ions. It also forms a zn complex with zinc chloride and nitrate ions. The thermolysis of furyl derivatives produces the corresponding anions. 5,6-DDA can also undergo a photochemical reaction with chlorine gas to form its molecular ion at 637 nm.</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>Please enquire for more information about 1-(4-Cyanophenyl)-2-nitropropene including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>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-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>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>3-Cyanopropionaldehydedimethylacetal (3CPDMA) is a reactive compound that inhibits the proliferation of muscle cells. It has been shown to inhibit the synthesis of 3-hydroxy-3-methylglutaryl coenzyme A, which is required for the production of cholesterol and fatty acids. This inhibition leads to a decrease in the growth of cells and their ability to divide. 3CPDMA has also been shown to have an inhibitory effect on picolinic acid, which is involved in the activation of receptors that induce cellular proliferation. The inhibition of this receptor may be due to its ability to compete with other ligands for binding sites on the receptor.<br>It has been shown that 3CPDMA acts as an antagonist against acarids, which are mites that feed on skin cells. This property may be due to its antagonistic effects on amino acid composition, which may affect calcium uptake by cells or cell membrane permeability.</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>4,5-Bis(2-cyanoethylthio)-1,3-dithiole-2-thione is a fluorescent compound that exists in two orientations, cis and trans. It has been used as a linker for the construction of new compounds with interesting properties. 4,5-Bis(2-cyanoethylthio)-1,3-dithiole-2-thione has been shown to be an effective ligand for palladium cross coupling reactions. This compound can also be used in supramolecular chemistry due to its ability to fluoresce brightly.</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-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>Tak-659 is an amide compound that inhibits the serine protease activity of a number of enzymes, including cathepsin B and L. Tak-659 has been shown to have inhibitory effects on inflammation in animal models by inhibiting the production of inflammatory cytokines. Tak-659 has also been shown to impair protein synthesis in gram-negative bacteria, such as Escherichia coli and Pseudomonas aeruginosa. The mechanism for this inhibition is not entirely clear but may be due to tak-659 binding to the ribosomal RNA near the peptidyl transferase center, blocking the entry of amino acids into the ribosome. Tak-659 binds with high affinity to adenosine receptors and has been shown to reduce levels of inflammatory cytokines in mouse tumor cells.</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>4-Cyano-4'-aminobiphenyl is a fluorescent dye that exhibits a strong fluorescence under UV irradiation. The dye has an absorption maximum at about 335 nm and a fluorescence emission maximum at about 455 nm, with excitation maxima of 333 nm and 478 nm. It has been used in the development of photocurrent devices, which are used for photochemical reactions and electrochemistry studies. This compound can also be used for the determination of amino groups in organic molecules such as carbostyril. The compound can be synthesized by reacting an amine with an aldehyde in the presence of acid.</p>

<p>Please enquire for more information about 2-(3-Cyano-1H-1,2,4-triazol-1-yl)acetic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2-(2-formyl-6-methoxyphenoxy)acetonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>7-Cyano-7-deazaguanosine is a nucleoside that belongs to the category of 7-deazapurines. It is an optimized nucleic acid analogue that has been shown to act as a translational inhibitor in vitro and in vivo. This compound has been shown to have high yields in chemical synthesis, which makes it an attractive candidate for optimization and future research. 7-Cyano-7-deazaguanosine is a synthetic nucleotide with anticodon properties, which may be useful for the development of new drugs against bacterial infections.</p>

<p>3,4-Difluoro-5-nitrobenzonitrile is a hepatotoxic compound that is found in the environment. It has been shown to cause cirrhosis and overgrowth of the liver. 3,4-Difluoro-5-nitrobenzonitrile also inhibits hepatic encephalopathy and may be used to treat liver disease. This toxicant has been detected in the bowel and duodenum of humans with nonalcoholic steatohepatitis, as well as in the jejunum and duodenum of mice with spontaneous steatohepatitis. It also causes nonalcoholic steatohepatitis when given orally to rats.</p>

<p>5-Methyl-1,3-thiazol-2-yl)acetonitrile is a chemical that is used as a building block in organic synthesis. It has been shown to be an intermediate in the preparation of other compounds and has been used as a research chemical. This chemical has also been shown to have useful properties, such as high quality and versatility. 5-Methyl-1,3-thiazol-2-yl)acetonitrile can be used as a reaction component or a reagent for synthesizing other chemicals.</p>

<p>3-Ethoxy-4-hydroxyphenylacetonitrile is a versatile building block and reagent that is used in the manufacturing of pharmaceuticals, agricultural chemicals, and other chemical products. It has been shown to be an excellent starting material for the synthesis of complex compounds. 3-Ethoxy-4-hydroxyphenylacetonitrile can be used as a high quality research chemical or useful scaffold for organic synthesis. CAS No. 205748-01-2</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>4-Aminophenylacetonitrile is a molecule that is structurally similar to nitrobenzene. 4-Aminophenylacetonitrile has been shown to be an efficient method for inhibiting faecalis growth and secretory phospholipase A2 (sPLA2) activity in vitro. It also inhibits the population growth of E. coli in vivo, which can be attributed to its ability to inhibit the enzyme catalysed by hydrogen bond formation.</p>

<p>2-(4-tert-Butyl-phenoxy)acetonitrile is a high quality, reagent, complex compound that is useful as a building block in the synthesis of fine chemicals and speciality chemicals. 2-(4-tert-Butyl-phenoxy)acetonitrile can be used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It has a CAS number of 50635-24-0. This chemical is also useful for research purposes.</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>

<p>5-Cyanoindole is a hydrophobic molecule that has been shown to have an inhibitory effect on the trifluoroacetic acid-induced fluorescence in the presence of chloride ions. It is also able to bind peptides and has been used as an antimicrobial peptide. 5-Cyanoindole can be synthesized electrochemically or by electrochemical impedance spectroscopy. The synthesis of 5-cyanoindole can be achieved through a Friedel-Crafts reaction, followed by a hydrolysis with hydrogen peroxide and then a reduction with sodium borohydride.<br>!-- END OF PRODUCT DESCRIPTION --&gt;</p>

<p>4-tert-Butylcalix[4]arene is a polymorphic compound with transport properties. It has been shown to have an activation energy of ˜30 kcal/mol, and can be characterized by its nmr spectra. The molecule can be found in n-hexane and zirconium. 4-tert-Butylcalix[4]arene is a coordination complex with a transfer mechanism that contains chloride or metal ion. It forms an acid complex with thermally stable molecules.</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>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>3-Hydroxyphenylacetonitrile is a molecule that is the precursor for a number of isothiocyanates, which are phytochemicals with antibacterial properties. It has been shown to have inhibitory effects on dopamine hydroxylase, an enzyme that catalyzes the conversion of dopamine to norepinephrine and epinephrine. 3-Hydroxyphenylacetonitrile also inhibits the activity of other active enzymes such as cytochrome P450. The inhibition of these enzymes by 3-hydroxyphenylacetonitrile may be responsible for its antibacterial properties. This molecule is inactivated by cyanides, which leads to its inability to produce any isothiocyanates. Kinetic studies show that 3-hydroxyphenylacetonitrile saturates at high concentrations, leading to decreased production of cyanide.</p>

<p>(S,E)-3-(6-Bromopyridin-2-yl)-2-cyano-N-(1-phenylethyl)acrylamide (MBI-23) is a potential antineoplastic agent that has been shown to induce regression of bladder cancer in mice. MBI-23 induces apoptosis by inhibiting the proliferation of cancer cells and inducing differentiation of cancer stem cells. It is also shown to inhibit tumor growth and progression in glioma and prostate cancer models. MBI-23 binds to the KDR receptor subtype, which is activated by organic acids and inhibited by inorganic compounds. This binding leads to constitutive activation of the KDR receptor, thereby inducing apoptosis. The tautomers and stereoisomers of MBI-23 have not been fully elucidated yet.</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>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>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-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>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>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>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>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-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>5-Bromo-2-cyano-3-nitropyridine is a medication that has been shown to be an effective inhibitor of the RET tyrosine kinase. It has been used in clinical studies to treat chronic kidney disease and has been shown to inhibit the growth of cancer cells. The molecular electrostatic potential (MEP) simulations have shown that 5-bromo-2-cyano-3-nitropyridine interacts with the reactive site of RET, inhibiting its function by binding to the nucleophilic substitutions. 5-Bromo-2-cyano-3-nitropyridine is synthesized from 2,5 dibromopyridine and 3 nitrobenzene at high yield. The molecule is chromatographically separated from impurities such as 4 bromo pyridine.</p>

<p>N-Cyanomorpholine is a synthetic compound that is used as a reagent in organic synthesis. It has been shown to form stable complexes with amines, such as aniline and pyridine. In addition, it can be used in the intramolecular hydrogenation of alkenes, which is catalyzed by palladium on carbon. N-Cyanomorpholine was found to be effective against some viruses, such as herpes simplex virus type 1 and influenza virus type A. It also has been validated for use in the synthesis of dianthus caryophyllus and acrylonitrile.</p>

<p>4-(Bromomethyl)benzylamine HBr is a fine chemical that can be used as a building block for organic synthesis. This compound is also a useful research chemical, reagent, and specialty chemical. 4-(Bromomethyl)benzylamine HBr has been used as a reaction component in the synthesis of various pharmaceuticals, such as theophylline and ampicillin. It has also been used as an intermediate in the production of other compounds, such as 4-hydroxybutyric acid and 3-methylthiopropionic acid. This complex compound can be purchased at high quality and is versatile enough to act as a scaffold for many reactions.</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>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>2,6-Dichlorophenylacetonitrile (2,6-DCPA) is a cyanide herbicide that controls weed growth. 2,6-DCPA is used as a preemergent herbicide and is applied to the soil before planting. It can be mixed with calcium oxide or other materials to form a dust, which is then applied to the soil surface. 2,6-DCPA inhibits plant growth by interfering with the photosynthesis process, which may be due to its high cytotoxicity. The exact mechanism of action has not been determined but it may be due to interference with chloride transport or ethyl esters production in plants. This chemical has also been shown to inhibit amine metabolism in plants and animals.<br>2,6-DCPA has two isomers: cis and trans. They differ only in the position of the chlorine atom on the benzene ring: cis (left) and trans (right).</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>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-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>3-Cyano-4,6-dimethylcoumarin is a phenolic compound with potent inhibitory activity against bacteria. It has been shown to bind to the hydroxyl group of the coumarin ring and inhibit the growth of Gram-negative and Gram-positive bacteria. 3-Cyano-4,6-dimethylcoumarin also inhibits the growth of fungi by binding to the hydroxyl group on a phenolic hydroxyl substituent. 3-Cyano-4,6-dimethylcoumarin can be used as an antimicrobial agent for various types of infections.</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-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>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>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>2,5-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>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>(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-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>Butyl cyanoacrylate is a cyanoacrylate, a type of monomer that reacts with water to form a polymer. Cyanoacrylates are used in sealants and tissue adhesives because they form strong bonds with tissues and are biocompatible. Butyl cyanoacrylate has been shown to have an exothermic reaction when it is mixed with water, which can cause burns if the user is not careful. This product also has toxicological studies on fetal bovine and mammalian tissue. Butyl cyanoacrylate has been shown to inhibit vasoactive intestinal peptide release in the nervous system, which may be due to its ability to interfere with fatty acid metabolism.</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>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>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>Please enquire for more information about [3-(2-Methylphenyl)-1,2,4-oxadiazol-5-yl]acetonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>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-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-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>N,N-Diethylcyanoacetamide is an organic compound that is used in the industrial production of polyurethane. It reacts with a nucleophile to form a new carbon-nitrogen bond. The reaction can be monitored in real time, and it has high specificity for the desired product. N,N-Diethylcyanoacetamide reacts with piperidine to produce a mixture of isomers in which the methyl group is attached to either the nitrogen or the oxygen atom. This mixture can be separated by crystallization, and it generates a pure product that can be used as a monocarboxylic acid.</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>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>5-Cyanoindole-3-carboxaldehyde is an aldehyde that is used in synthesis of β-unsaturated aldehydes. It is prepared by the reaction of 3-cyanoindole with formaldehyde. 5-Cyanoindole-3-carboxaldehyde has antibacterial activity against gram positive and gram negative bacteria. It also has a high yield and can be purified by filtration or by condensation with chlorobenzene. 5-Cyanoindole-3-carboxaldehyde can be activated by irradiation, which makes it useful for the production of pharmaceuticals.</p>

<p>N'-(2-Cyano-4-fluorophenyl)-N,N-dimethylimidoformamide is a high quality, reagent that is useful for the synthesis of complex compounds. It can be used as a fine chemical and speciality chemical in research and development. The CAS number for this compound is 1017082-62-0. N'-(2-Cyano-4-fluorophenyl)-N,N-dimethylimidoformamide has shown to be a versatile building block for the synthesis of novel compounds that are not commercially available. This product is suitable for use in reaction components as well as being an intermediate for the synthesis of other compounds.</p>

<p>4-Aminobenzonitrile is a chemical compound that has been shown to be an antimicrobial agent. It has been found to be active against bacteria and fungi, such as Candida albicans and Aspergillus niger. 4-Aminobenzonitrile binds with epidermal growth factor (EGF) by intramolecular hydrogen bonding, which leads to the disruption of the protein's tertiary structure. The nitrogen atoms in this compound have been shown to react with water vapor at high temperatures, which results in the release of hydrogen gas. This reaction can be used for phase transition temperature studies. 4-Aminobenzonitrile also shows intermolecular hydrogen bonding with fatty acids, which causes the molecule to change its shape and protonation state. These changes affect its frequency shift and molecular modeling study results.</p>

<p>5-Cyano-1H-indole-2-carboxylic acid is a high quality reagent that is used as an intermediate in the synthesis of complex compounds. It can also be used as a building block for the synthesis of speciality chemicals and research chemicals. The versatile nature of this compound makes it useful as a reaction component in the synthesis of many different types of compounds, including fine chemicals and pharmaceuticals. 5-Cyano-1H-indole-2-carboxylic acid is available commercially with CAS No. 169463-44-9.</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>