Ciano-, nitrilo-

<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>Dodeca 2E,4E,8Z,10E,Z-tetraenoic acid isobutylamide (DETBA) is a versatile building block that is used in the synthesis of natural products and pharmaceuticals. DETBA can be used as a reaction component in organic synthesis to form complex compounds such as polyesters, polyamides, polyurethanes, and polyimides. It also has high quality and can be used in research or speciality chemical applications.</p>

<p>Lasalocid A sodium salt is a sodium salt of lasalocid, which is a macrolide antibiotic that inhibits bacterial growth by binding to the 50S ribosomal subunit. Lasalocid A sodium salt has intramolecular hydrogen bonds and exhibits high solubility in acetonitrile. The experimental solubility data was obtained using an analytical method with quillaja saponaria as a model system. Lasalocid A sodium salt has been used as an experimental model for congestive heart failure and is also used in biological samples such as blood, urine, or tissue. This drug is highly resistant to degradation by bacteria.</p>

<p>Ethyl 4-cyano-3-nitrobenzoate is a chemical compound with the structural formula of CHNO. It is a building block for organic synthesis and can be used in the production of high quality research chemicals and speciality chemicals. Ethyl 4-cyano-3-nitrobenzoate has been shown to react with a variety of amines to form urea derivatives that are useful as versatile building blocks or complex compounds. This reagent is also useful as an intermediate in the synthesis of various pharmaceuticals. CAS No. 321162-58-7</p>

<p>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>

<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>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>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-(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>

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<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>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>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>2'-Cyano-4-(dibromomethyl)biphenyl is a reactive component that belongs to the group of speciality chemicals. It can be used as a building block in organic synthesis and as an intermediate in the production of fine chemicals. 2'-Cyano-4-(dibromomethyl)biphenyl has been used for the synthesis of various complex compounds, such as an anti-inflammatory drug, an anti-diabetic drug, and a chemotherapeutic agent.</p>

<p>7-Cyano-7-deaza-2’-deoxyguanosine is a pyrrole nucleoside analog that has been shown to inhibit the replication of herpes simplex virus type 1 and 2 in human cell lines. 7-Cyano-7-deaza-2’-deoxyguanosine is a synthetic nucleoside analog that is structurally similar to deoxyadenosine, but with a cyanide group instead of an oxygen atom. This compound has been shown to have the same biochemical properties as deoxyadenosine, including inhibiting the incorporation of uridine into RNA and DNA. In addition, 7-Cyano-7-deaza-2’-deoxyguanosine inhibits the synthesis of proteins from amino acids by competitive inhibition of ribonucleotide reductase, which catalyzes the conversion of ribonucleotides to deoxyribonucleotides. The enzyme's function</p>

<p>1,4-Diamino-2,3-dicyanoanthraquinone is a chemical compound that belongs to the amines group. It has transcription-polymerase chain activity and inhibits the growth of cancer cells by regulating blood pressure and stimulating the production of growth factors. The effect on cancer cells is due to its ability to inhibit kinases. 1,4-Diamino-2,3-dicyanoanthraquinone has shown an inhibitory effect on glutamate decarboxylase and fatty acid synthase, which are enzymes that regulate cell metabolism. This chemical compound also exhibits quinoline derivatives with a redox potential that can be used as hydrogen chloride in organic synthesis reactions.</p>

<p>The 4-cyanoindole is a fluorescent molecule that binds to proteins and affects protein homeostasis. It has been shown to bind to the sodium salt form of proteins, which are typically found in human liver cells. The binding of 4-cyanoindole to these proteins leads to its reduction by borohydride and fluorescence resonance energy transfer (FRET) between the molecule and the protein. This binding can be detected using a fluorescence lifetime spectroscopy technique, which detects changes in the fluorescence's lifetime as well as intensity. The binding of 4-cyanoindole to proteins has been shown to have anti-cancer properties. It has also been used for detection of monoclonal antibodies against cancer cells or for fluorescent labeling of cancer cells for immunofluorescent microscopy.</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>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>2-Methoxyphenylacetonitrile is a chemical that is used in the manufacture of pharmaceuticals. It has antibacterial activity and can be used to treat typhoid fever, staphylococcal infections, and mental disorders such as schizophrenia. 2-Methoxyphenylacetonitrile is an alkylating agent that reacts with nucleophiles in proteins, DNA, and RNA. These reactions lead to the destruction of the bacterial cell wall and inhibition of protein synthesis. The mechanism by which 2-methoxyphenylacetonitrile exerts its antibacterial effect may involve formation of a reactive intermediate that inhibits bacterial ribonucleotide reductase. The addition of an electron to this intermediate leads to the formation of a covalent bond with one or more amino acids in the protein acceptor, thereby preventing further growth and division of bacteria.</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>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>4-Bromobenzylamine is a chemical compound that has been used to study the process optimization of sephadex g-100. It is also used as a chemotherapeutic treatment for cancer. 4-Bromobenzylamine binds to intracellular targets, such as nitrogen atoms and cell lysis, with physiological levels found in fetal bovine serum. The nitrogen atom is an essential structural component of 4-bromobenzylamine that is necessary for its biological activity and may be involved in binding to DNA polymerase. This drug has been shown to inhibit the growth of metastatic colorectal cancer cells by inhibiting cellular proliferation. Structural analysis has revealed that 4-bromobenzylamine interacts with the polymerase chain reaction (PCR) enzyme and inhibits the ability of DNA polymerases to add nucleotides to the growing strand of DNA.</p>

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

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

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

<p>N-Allyl-N-(4-cyano-2-chlorophenyl)acetamide is a high quality reagent that has been used as an intermediate in the synthesis of fine chemicals, useful scaffolds and building blocks. It is also a versatile building block that can be used to synthesize high quality compounds with a wide range of functionalities. N-Allyl-N-(4-cyano-2-chlorophenyl)acetamide is a speciality chemical that can be used for research purposes. This compound has been shown to produce reactions with other compounds, such as nitrobenzene, to generate useful products.</p>

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

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

<p>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-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>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>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>m-Hydroxybenzonitrile is a cationic surfactant that has the ability to form hydrogen bonds with an intramolecular hydrogen. It is used in the production of detergents, textile processing aids, and inks. m-Hydroxybenzonitrile inhibits fatty acids by forming an inhibitory complex at the surface of the cell membrane. This complex disrupts lipid bilayers and inhibits protein synthesis. m-Hydroxybenzonitrile also has been shown to have vibrational properties that can be seen when it absorbs ultraviolet light.</p>

<p>2-Amino-4-fluorobenzylamine dihydrochloride is a research chemical that is used as a reactant in organic synthesis. 2-Amino-4-fluorobenzylamine dihydrochloride is an intermediate for the preparation of other chemicals and can also be used as a building block for more complex compounds. This chemical has been shown to have good quality and can be used in many different types of research.<br>2-Amino-4-fluorobenzylamine dihydrochloride has CAS number 606139-20-2.</p>

<p>2,4,6-Trichlorobenzonitrile is a chlorine-containing chemical that has been used as a pesticide. It is a highly toxic substance and can be fatal if ingested. 2,4,6-Trichlorobenzonitrile is converted to chloride in soil and water by microbial action. This chemical can be activated by light or temperature changes and is used in the production of pesticides that are phytotoxic. It also has been shown to have thermodynamic properties that allow it to act as an environmental pollutant. 2,4,6-Trichlorobenzonitrile can react with sulfoxides to form chloromethylation products such as 2,3,5-trichloroethanol. These reactions are catalyzed by metal ions such as Fe(II) and Mn(II).</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-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>

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<p>2-Bromophenylacetonitrile is a synthetic compound that is used in wastewater treatment. It is effective at removing cyanides, phenylpropionic acid, and aldehydes from wastewater. 2-Bromophenylacetonitrile has been shown to be an efficient method for the removal of liriodenine from sewage water and for the removal of 2-bromostyrene from industrial waste water. This process can be used as an analytical method to measure the concentration of these substances in samples of wastewater. The reaction mechanism involves the formation of a nitrilium ion intermediate and subsequent reactions with alcohols to form esters or ethers.</p>

<p>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>

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<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>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 [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>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'-octylbiphenyl is a molecule that consists of an aromatic ring with two alkyl chains. This compound has been shown to be a model system for studying solute transport in liquids and gases. 4-Cyano-4'-octylbiphenyl also has the ability to form intramolecular hydrogen bonds, which are important for the fluidity of the substance. At high temperatures, this compound undergoes a phase transition from liquid to solid due to dipole interactions between molecules.</p>

<p>tert-Butyl 4-cyanobenzylcarbamate (tB4Cbz) is a high quality chemical that can be used as a reagent, complex compound, or useful intermediate in the production of fine chemicals. Tert-Butyl 4-cyanobenzylcarbamate is also a useful scaffold for the synthesis of speciality chemicals and research chemicals. It can be used as a versatile building block for reactions involving amides, nitriles, esters, and amines.</p>

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<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>