Cyano-, Nitrile-

<p>7-(Cyanomethoxy)indole is a versatile building block that can be used as a scaffold for the synthesis of complex molecules. It has been used as an intermediate in organic synthesis and as a reaction component for the preparation of useful compounds. 7-(Cyanomethoxy)indole is also known to have high quality and is widely used in research laboratories.</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-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-3-methylbenzonitrile is a high quality chemical that is used as an intermediate in the synthesis of complex compounds. It can be used as a reagent in organic chemistry, and has been shown to be useful for the production of fine chemicals, such as antibiotics. 2-Hydroxy-3-methylbenzonitrile is also a versatile building block for the production of pharmaceuticals and research chemicals. It can be used as a reaction component for the synthesis of speciality chemicals and various building blocks.</p>

<p>3-Cyano-4-methoxybenzoic acid is a white crystalline solid that is soluble in water. This compound is a useful intermediate for the synthesis of other organic compounds, as well as a useful scaffold for the synthesis of complex compounds. 3-Cyano-4-methoxybenzoic acid also has potential use as a research chemical, and can be used as an effective building block for the preparation of fine chemicals.<br>3-Cyano-4-methoxybenzoic acid may be used to produce speciality chemicals such as pharmaceuticals, dyes, pesticides, and perfumes. It can also be used to synthesize compounds with diverse functionalities.</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>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>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>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>2,4,6-Trimethoxybenzonitrile is a ligand that forms coordination complexes with metal ions. It can be used to make N-oxide compounds and reaction products with aryl chlorides. The 2,4,6-trimethoxybenzonitrile ligand has been shown to form cross-coupling complexes with benzotriazolyl. This compound is soluble in organic solvents and has a vapor pressure of 0.0025 mm Hg at 25°C. The molecular weight of this compound is 196.2 g/mol and its melting point is 190°C. 2,4,6-Trimethoxybenzonitrile has a symmetric molecule in the gas phase and an asymmetric molecule in solution due to the interactions of hydrogen bonding and van der Waals forces.</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>[(4-Methylphenyl)sulfonyl]acetonitrile is a synthetic compound that has been shown to inhibit the enzyme SHP2. This inhibition leads to decreased proliferation of cells and may be useful in the treatment of degenerative diseases. [(4-Methylphenyl)sulfonyl]acetonitrile is an organic solvent and a nucleophilic reagent that reacts with metal carbonates, such as calcium carbonate, to form carbanions. The carbanion intermediate can react with nucleophiles, such as acetonitrile, to form a new compound that is structurally related to the original starting material.</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>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>N-Nitrosodibenzylamine is a chemical compound that has genotoxic effects. It is used as an analytical method to identify the presence of amines and to measure their concentration, as well as in the preparation of sodium salts. N-Nitrosodibenzylamine was found to cause damage to DNA in animals and cells in culture. The matrix effect, which is the difference in response between a sample contained in an organic solvent and one contained in water, was investigated using multi-walled carbon nanotubes (MWCNTs). The results showed that MWCNTs produce a significant matrix effect when compared with other solvents. This study also showed that MWNTs have a higher capacity for nitrosamine adsorption than do other solvents.</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>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-(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>Mesitylacetonitrile is a mesityl-substituted acetonitrile. It is used in organic synthesis as a Grignard reagent, which is an organometallic compound containing an alkyl or other carbon group bound to magnesium. Mesitylacetonitrile has been shown to react with chlorides to produce furyl chlorides and chloride. Mesitylacetonitrile can be synthesized by reacting phenylacetonitrile (a byproduct of the synthesis of acetone) with chlorine gas and hydrogen in the presence of a catalyst such as copper(II) chloride. This reaction produces mesitylacetonitrile and hydrogen chloride gas as byproducts. The compound has been used to synthesize corticotropin-releasing factor receptor antagonists that have potential therapeutic applications for the treatment of stress-related disorders.</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-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>

<p>Ethyl 2-cyano-3-(4-nitrophenyl)prop-2-enoate is a functionalized molecule that contains a dipole. It has high selectivity for 1,3-dipolar cycloadditions because the electron density of the methylene group is greater than that of the aldehyde group. The mechanistic theory for this reaction is that the electron density on the methylene group in ethyl 2-cyano-3-(4-nitrophenyl)prop-2-enoate will cause it to become more reactive than the aldehyde group. The dipoles in this molecule are oriented such that they can react with each other to form an intermediate and then an adduct. This isomerization occurs through either dipolarophilic or electrocyclic mechanisms.</p>

<p>2-Amino-6-methoxybenzonitrile is an organic compound that belongs to a group of monosubstituted hydroxylamines. It has been used in the synthesis of various analogues, such as caprolactam and methoxyanthranilic acid. Hydrochloric acid reacts with 2-amino-6-methoxybenzonitrile to form 2-amino-6-hydroxybenzonitrile, which can be oxidized to 2-amino-6-(hydroxymethyl)benzonitrile. This reaction is catalyzed by copper or zinc metal.</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>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>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>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>2,6-Difluorobenzonitrile is a nucleophilic compound that reacts with inorganic acids to form new chemical structures. It has been shown to react with hydrochloric acid, sodium carbonate and phosphotungstic acid. The FT-IR spectroscopy of 2,6-difluorobenzonitrile shows a reaction product with a proton. This means that the molecule is able to transfer a hydrogen ion from one site to another. The reaction between 2,6-difluorobenzonitrile and sodium carbonate produces an insoluble precipitate of sodium phosphate and sodium chloride, which can be analyzed gravimetrically. 2,6-Difluorobenzonitrile has also been shown to have fluorescence properties that are activated by ultraviolet light and naphthalene.</p>

<p>Please enquire for more information about Barium tetracyanoplatinate(II) hydrate including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>Cypermethrin is an insecticide that belongs to the family of chemical pesticides. It is used in agriculture and in public health to control malaria-transmitting mosquitoes, head lice, and scabies mites. Cypermethrin disrupts the insect nervous system by inhibiting the function of synapses between nerves, resulting in paralysis and death. The compound also affects signal pathways that regulate locomotor activity and enzyme activities. Cypermethrin has been shown to have a high resistance to degradation by glycol ethers such as ethylene glycol monomethyl ether acetate (EGMEA). It has an optimum concentration of 0.01 ppm for mosquito control and 0.1 ppm for lice control. The analytical method involves liquid chromatography with sodium citrate as an ion-pairing agent and a linear calibration curve using a standard curve generated from known concentrations of cypermethrin.</p>

<p>4-Hydroxy-3-methoxybenzylamine hydrochloride is a reagent, complex compound and useful intermediate for the production of speciality chemicals. CAS No. 7149-10-2 is not a hazardous chemical and does not pose any significant risk to human health or the environment when used as intended. This chemical has many uses including being a useful scaffold in organic synthesis, a useful building block for the preparation of other compounds, and a versatile building block for the preparation of various compounds. It also has many applications in research such as being an intermediate for the synthesis of other compounds, or as a reactant in various reactions.</p>

<p>Benzenesulphonylacetonitrile is an alkanoic acid nucleophile with a benzimidazole derivative. It has shown potential for use as a cancer drug by inhibiting tumor-associated enzymes and inducing apoptosis in cancer cells. Benzenesulphonylacetonitrile is also active against inflammatory diseases such as rheumatoid arthritis, psoriatic arthritis, and Crohn's disease. This drug can be synthesized by the reaction of sodium salts with benzenesulphonylacetone followed by a nucleophilic substitution reaction with methylene chloride. The synthesis of benzenesulphonylacetonitrile requires anhydrous acetonitrile and palladium-catalyzed coupling reactions in the presence of sodium carbonate. Benzenesulphonylacetonitrile has chemical stability in the presence of acids, bases, and heat.br&gt;</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-(2,3-Dichlorophenyl)-2-guanidinyliminoacetonitrile (2,3-DCPP) is a high quality reagent that is used in the preparation of complex compounds. It is also an intermediate in the synthesis of fine chemicals and useful scaffold and building block for research chemical. 2,3-DCPP has been shown to react with a variety of functional groups including amines, alcohols, thiols, carboxylic acids, organometallic reagents and many others. It is also a versatile building block for the synthesis of chemical substances such as pharmaceuticals, agrochemicals or dyes.</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>2-Chloro-4-fluorobenzonitrile is a drug that has been shown to have antitumor effects by binding to the CB2 receptor. It inhibits hydrogenation reduction of the molecule, which may be due to its ability to react with both functional groups. 2-Chloro-4-fluorobenzonitrile has also been shown to inhibit progesterone receptor, which may lead to an increase in progesterone levels and a decrease in estrogen levels. The pharmacokinetic properties of this compound are not yet known.</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>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>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>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>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>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>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>N-(5-Cyano-2-chlorophenyl)acetamide is a high quality, reagent, and versatile building block. It is a fine chemical that can be used as a building block for the synthesis of other compounds. N-(5-Cyano-2-chlorophenyl)acetamide is also a speciality chemical that can be used in research or as a reaction component. It has been found to be useful as an intermediate in the synthesis of complex compounds.<br>END&gt;</p>

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

<p>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>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>