Ciano-, Nitrile-

4-Chloro-3,5-dinitrobenzonitrile is a mesomeric compound that has four amines and one nitro group. It is a dipole with chloride as the negative end and amine as the positive end. The reaction mechanism of this chemical is nucleophilic substitution. 4-Chloro-3,5-dinitrobenzonitrile reacts with an organic solvent to form a buffer. A buffer is an ionized solution that resists changes in pH when acid or base are added to it. This chemical also reacts with thionyl chloride to form hydrochloric acid, which can be used to leishmania parasites. 4-Chloro-3,5-dinitrobenzonitrile also reacts with an anion such as ClO4− or NO2− to form a salt such as chlorate or nitrate respectively.

<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>4-Cyano-2-hydroxybenzaldehyde is a high quality chemical that can be used as a reagent and intermediate in the synthesis of complex compounds. It is also an important building block in the synthesis of fine chemicals. 4-Cyano-2-hydroxybenzaldehyde has been used as a versatile building block in the synthesis of organic compounds, useful scaffolds in medicinal chemistry, and reactive intermediates. It has also been shown to have anti-inflammatory properties and may be a potential treatment for inflammatory bowel disease.</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>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>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>

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

<p>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>4-(Benzyloxy)-3-methoxyphenylacetonitrile is an anti-cancer drug that belongs to the class of dihydroisoquinolines. It is used as a monomer in the synthesis of other drugs and it has been shown to be an effective inhibitor of cancer cells when used with carbamic acid. 4-(Benzyloxy)-3-methoxyphenylacetonitrile is synthesised through the reaction of 2,4-dichloroisonicotinic acid and 3-fluoroacetamide in the presence of a strong acid catalyst. This compound has been shown to have a high level of stereoselectivity, which makes it useful for synthesising other compounds.</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-Hydroxyphenylacetonitrile (HPA) is a chemical compound that belongs to the group of nitriles. It is a precursor to the pigment sinalbin, which is found in corynebacterium and related bacteria. HPA has been shown to have an apoptotic effect on human cells, which may be due to its ability to inhibit protein synthesis and induce DNA fragmentation. The synthetic pathway for HPA starts with the conversion of L-phenylalanine into 4-hydroxyphenylpyruvic acid by a wild-type strain or bacterial strain. The 4-hydroxyphenylpyruvic acid is then converted into 4-hydroxybenzaldehyde through polymerase chain reactions or expression plasmids in corynebacterium glutamicum. This molecule can then be transformed into HPA by hydrolysis with hydrochloric acid or enzymatic activity. HPA has also been shown to stimulate</p>

<p>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>

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>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>

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>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>

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>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>

Lobetyolin is a phenolic compound that has been found to be an inhibitor of monoamine oxidase. Lobetyolin is an acetylated derivative of 4-hydroxy-3-methoxyphenylacetonitrile. It has been shown to inhibit bacterial growth in vitro, with the exception of Mycobacterium tuberculosis and Mycobacterium avium complex. The optimal reaction time for lobetyolin is 3 hours at a pH between 7 and 8, with a yield of 66% at room temperature. Lobetyolin reacts rapidly with amines, alkylating them as it undergoes oxidation by hydrogen peroxide. Lobetyolin also reacts slowly with dopamine and aldehydes, but more readily with chlorides, yielding lobetyrine and chloroacetaldehyde respectively.

<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>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>

Phenoxyacetonitrile is an efficient method for the synthesis of ethylene diamine by the reaction of hydrochloric acid, chloride and a carbon source. The nitro group can be reduced to an amine or a hydroxyl group by hydrogen chloride in acetonitrile. This method has been used in the synthesis of drugs such as acyclovir and penciclovir. Phenoxyacetonitrile also inhibits growth factor production, which may be due to its inhibitory properties on the enzyme houben-hoesch reaction.

<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>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>

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>Please enquire for more information about Ethyl (2Z)-2-cyano-3-(2-furyl)acrylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</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. 2-Amino-4-fluorobenzylamine dihydrochloride has CAS number 606139-20-2.

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>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>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-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>

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>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>

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>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>(2,3-Dichlorophenyl)acetonitrile is a fine chemical that is useful as a building block in the synthesis of more complex compounds. It has been used in research as a reagent and as a speciality chemical. (2,3-Dichlorophenyl)acetonitrile reacts with many different types of compounds to form new molecules. This intermediate can be used in the synthesis of many different types of compounds and also serves as an important scaffold for larger molecules.</p>

<p>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>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>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>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>

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. 2-Chloro-5-cyanopyrazine can be synthesized from benzene and chloropicrin in the presence of copper(II)

<p>Methyl-4-cyanobenzoate is a nucleophilic compound that reacts with electrophilic functional groups. It is used in organic chemistry as an immobilized reagent for the conversion of alcohols, amines, and thiols to their corresponding halides. Methyl-4-cyanobenzoate has been shown to have anti-inflammatory properties by inhibiting neutrophil migration into cutaneous tissue and reducing the production of proinflammatory compounds such as isobutene and naphthalene. It also inhibits the release of histamine from mast cells.</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-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>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>

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

<p>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>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>

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>

<p>4-Amino-2-chlorobenzonitrile (4ACB) is a copper salt that can be used in antimalarial therapy. It has been shown to have strong antiplasmodial activity against the parasite Plasmodium falciparum and other species of the genus Plasmodium. 4ACB is synthesized by nitro group reduction and ammonolysis, followed by an addition reaction with chloroformate. 4ACB binds to the enzyme ferredoxin reductase and inhibits electron transfer, which leads to inhibition of ATP production and cell death. The molecular modelling study showed that 4ACB is a reactive molecule with high affinity constants for copper ion.</p>

<p>Substrate of benzylamine oxidase and monoamine oxidase B</p>

<p>1-Adamantyl acetonitrile is a trifluoroacetic acid derivative that is used in the synthesis of 4-aminoantipyrine, chlorides, acid chlorides, and acetonitrile. 1-Adamantyl acetonitrile can be used to produce a variety of pharmaceuticals, such as aliphatic carboxylic acids, aldehydes, and amide. It can also serve as a reactant for reactions with alcohols or amines.</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>3,4-Diethoxyphenylacetonitrile is an intermediate that is used in the synthesis of drotaverine. It can also be used to synthesize catechol, which is a medicine used to treat depression and anxiety. 3,4-Diethoxyphenylacetonitrile can be chloromethylated with phosphorus pentachloride to produce 3,4-diethoxyphenylacetic acid. This product has been used in the synthesis of sodium cyanide and catechol hydrochloride.</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>

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>3,4-Dihydroxybenzylamine hydrobromide is a chemical that reacts with hydrogen peroxide to produce light. It is used as a nutrient for the chemiluminescent reaction in a nutrient solution to detect dopamine, chlorogenic acids, and trifluoroacetic acid. 3,4-Dihydroxybenzylamine hydrobromide can also be used as an analytical method for the measurement of cortisol concentration in plasma and saliva samples. This chemical analogically reacts with monoamine neurotransmitters such as dopamine and gamma-aminobutyric acid (GABA) to form fluorescent probes. 3,4-Dihydroxybenzylamine hydrobromide is not toxic or mutagenic and has been shown to be safe for use in humans.</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>3-Cyanobenzoic acid ethyl ester is a reaction component that is used in organic synthesis. It is a versatile building block, useful intermediate, and useful building block. 3-Cyanobenzoic acid ethyl ester is a fine chemical that can be used as a reagent for the preparation of other compounds. This compound has been assigned CAS No. 2463-16-3 and has the molecular formula C7H6O2.</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>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>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>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>

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.

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>Ethyl (3-amino-3-cyanopropyl)methylphosphinate is a versatile building block that can be used as a reagent, speciality chemical, or research chemical. It is useful as an intermediate for complex compounds and can be used as a reaction component in the synthesis of high quality compounds. Ethyl (3-amino-3-cyanopropyl)methylphosphinate is also a useful scaffold in organic synthesis.</p>

<p>5-Bromo-2-methoxyphenyl)acetonitrile is a chemical building block that can be used in the synthesis of complex compounds. It is a versatile intermediate that can be used as a reagent in organic reactions. This compound has been shown to be useful as a reaction component and is a high quality product. 5-Bromo-2-methoxyphenyl)acetonitrile has CAS number 7062-40-0 and is listed on the Chemical Abstracts Service (CAS).</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>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>3,5-Dimethoxyphenylacetonitrile is a synthetic compound that has been shown to be an inhibitor of the demethylation reaction. It is postulated to have anticancer activity and inhibits the biosynthesis of octaketides in vitro. This compound has also been shown to have antibacterial activity and is structurally related to cannabinoids. The mechanism by which 3,5-dimethoxyphenylacetonitrile inhibits cancer cells is not known. However, it may be due to its ability to bind cannabinoid receptors.</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>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>4-Cyanobenzamide is a naphthalene derivative that is both reactive and intramolecular. It has been shown to react with the amino group of peptides, forming a ruthenium complex. The functional groups are acceptors and donors that can be used in assays for the detection of anions or cations. 4-Cyanobenzamide reacts with water to release hydrogen gas, which can be used to measure its hydration ability. This compound has been synthesized using solid-phase synthesis and it has amide bonds that vibrate at a specific frequency.</p>

<p>Please enquire for more information about 2-Cyano-N-[2-(3,4-dimethoxyphenyl)ethyl]acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>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>

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 (>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>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>2-Cyanoacetamide is an organic compound that is used in pharmaceutical preparations. It reacts with malonic acid to form a dioxime, which is a precursor of various drugs. The optimum concentration for the reaction to occur is at 10% (w/v). The reaction mechanism has not been fully elucidated and it involves the transfer of nitrogen from an amide group to a carbonyl group. 2-Cyanoacetamide has shown anti-angiogenic effects in mice by inhibiting the expression of Mcl-1 protein, which is involved in the regulation of apoptosis and inflammation. This drug also has biological functions as a precursor for dopamine, which helps regulate motor and cognitive functions.</p>

<p>5-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>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>

3-Methoxy-4-methylbenzonitrile is a reagent that is used in the synthesis of complex compounds, such as pharmaceuticals and fine chemicals. It has been shown to be useful as an intermediate for the synthesis of various drugs, including antibiotics. 3-Methoxy-4-methylbenzonitrile has also been shown to be a useful scaffold for the synthesis of new drugs and other chemical compounds. This compound is listed on the Chemical Abstracts Service registry number 3556-60-3.

<p>3-Cyanobenzylamine HCl is a high quality chemical that is used as a reagent, intermediate, or building block in the synthesis of complex compounds. It is a fine chemical and speciality chemical that may be used as a research chemical and versatile building block for the synthesis of organic compounds. 3-Cyanobenzylamine HCl has been shown to react with other chemicals to form useful scaffolds and building blocks, such as amides, amino acid esters, and ureas.</p>