Ciano-, Nitrilo-

<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-(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>2-Amino-5-chlorobenzonitrile is a potent inhibitor of butyrylcholinesterase (BChE) and has been shown to inhibit the activity of this enzyme in cell lung cancer and muscle. 2-Amino-5-chlorobenzonitrile also inhibits the activity of other enzymes, such as acetylcholinesterase (AChE) and phosphatidylcholine esterase (PCE), that are found in the membranes of cells. This inhibition leads to increased levels of acetylcholine in the synaptic cleft, which may lead to an increase in muscular contractions. 2-Amino-5-chlorobenzonitrile is also a product yield enhancer for chromene synthesis.</p>

<p>4-Amino-2-cyanotoluene is a quinazoline compound that inhibits the synthesis of thymine, which is necessary for DNA replication. This compound binds to the enzyme thymidylate synthetase, thereby inhibiting the synthesis of thymine. The inhibitory effect has been shown in a study using calf thymus DNA. 4-Amino-2-cyanotoluene also inhibits the synthesis of other nucleic acids such as adenine and guanine.</p>

<p>4-Amino-3,5-dichlorobenzylamine dihydrochloride is a chemical intermediate that can be used as a reagent for the synthesis of other compounds. 4-Amino-3,5-dichlorobenzylamine dihydrochloride is considered to be a high quality chemical with versatile uses. It is listed in the Chemical Abstracts Service (CAS) registry under 164648-75-3, and can be obtained from various suppliers.</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>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>4-Cyano-2-fluorobenzyl alcohol is a reagent that is used to produce chlorine and hydrochloric acid. It is also used industrially in the production of potassium chloride, a compound that is used in fertilizers, animal feed supplements, and water treatment. 4-Cyano-2-fluorobenzyl alcohol reacts with chloride ions to form hypochlorous acid (HOCl), which then reacts with water to form hydrogen chloride gas. The reaction with fluoride ions leads to the formation of hydrofluoric acid (HF).</p>

<p>2-Benzyloxyphenylacetonitrile is a compound that is used in the manufacture of polyester, fibre and crystallized products. It is also used as a solvent for dyes and oils, as well as an industrial chemical intermediate. 2-Benzyloxyphenylacetonitrile can be thermolysed to produce benzoic acid, which can then be oxidized to produce phenol. The residue obtained from this process has been found to have a calorific value of around 2500kcal/kg. This substance has been found to react with oxygen at high temperatures and form an oxygenated product.<br>2-Benzyloxyphenylacetonitrile can be synthesised by reacting benzene with styrene in the presence of water and a catalyst such as sodium hydroxide or calcium oxide. The reaction produces hydrogen gas, benzoic acid and 2-benzyloxyphenylacetonitrile.</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-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>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>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>4-Cyclohexyphenol is a natural compound that belongs to the class of compounds known as phenols. It has a hydroxyl group and an intramolecular hydrogen bond. The thermal expansion of 4-cyanophenol is approximately 6.6 × 10−6/°C, which is greater than the thermal expansion of p-hydroxybenzoic acid (approximately 1.8 × 10−6/°C). The reaction mechanism for 4-cyanophenol involves intramolecular hydrogen bonding, which leads to its rapid degradation. 4-Cyanophenol reacts with trifluoroacetic acid in the presence of sodium carbonate to form p-hydroxybenzoic acid, which can be determined by measuring its absorbance at 290 nm. Hydrogen bonding interactions with the surface are responsible for the high sensitivity and selectivity of this analytical method.<br>4-Cyanophenol may also be detected using plasma mass spect</p>

<p>4-Chloro-3-nitrobenzonitrile is a molecule with potent antibacterial activity. It is synthesized by the reaction of sodium carbonate, hydrogen chloride, and 4-chlorobenzonitrile. 4-Chloro-3-nitrobenzonitrile has shown antimicrobial properties against a wide range of bacteria, including methicillin resistant Staphylococcus aureus (MRSA) and Enterococcus faecium. This compound has been used in the treatment of infections caused by these bacteria. 4-Chloro-3-nitrobenzonitrile also has the ability to inhibit the synthesis of fatty acids and lipids in bacterial cells, which may be responsible for its antimicrobial effects.</p>

<p>3-Cyanobenzamide is an organic compound with the formula CHC(N)NH. It is a white crystalline solid that can be obtained by reacting benzamide with cyanoacetylene. There are three possible isomers of 3-cyanobenzamide: 3-cyano-1-(substituted phenyl)benzamide, 3-cyano-2-(substituted phenyl)benzamide, and 3-cyano-3-(substituted phenyl)benzamide. The optimal reaction conditions for the synthesis of 3-cyanobenzamide are in the presence of hydrogen bonding, such as n-hexane, amide, and phase equilibrium. Studies have determined that 3-cyanobenzamide has the potential to cause cancer or liver toxicity in humans. In addition, this chemical has been shown to be an effective inhibitor of alpha glucosidase enzymes in vitro and in vivo.</p>

<p>3,4-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>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>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-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>