Cyano-, Nitrile-

<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>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>5-Bromo-2-cyano-3-nitropyridine is a medication that has been shown to be an effective inhibitor of the RET tyrosine kinase. It has been used in clinical studies to treat chronic kidney disease and has been shown to inhibit the growth of cancer cells. The molecular electrostatic potential (MEP) simulations have shown that 5-bromo-2-cyano-3-nitropyridine interacts with the reactive site of RET, inhibiting its function by binding to the nucleophilic substitutions. 5-Bromo-2-cyano-3-nitropyridine is synthesized from 2,5 dibromopyridine and 3 nitrobenzene at high yield. The molecule is chromatographically separated from impurities such as 4 bromo pyridine.</p>

<p>3-Cyanophenylacetic acid is a versatile building block and useful intermediate that can be used in the synthesis of a wide range of organic compounds. 3-Cyanophenylacetic acid is a fine chemical with CAS No. 1878-71-3 that can be used as a research chemical, reaction component, or speciality chemical. It is an important reagent for making complex organic compounds. 3-Cyanophenylacetic acid is a high quality product with the following characteristics: <br>1) Colorless crystals; <br>2) Soluble in water; <br>3) Soluble in acetone; <br>4) Slightly soluble in ether; <br>5) Reactivity: stable to heat, light, and air; <br>6) pH (1% solution): 2.0 - 4.0; <br>7) Melting point: 129 °C; <br>8) Boiling point: 188 °C at 760 mmH</p>

<p>4-Nitrobenzylamine hydrochloride is a bifunctional immobilizing agent that can be used for the immobilization of Zn2+. It reacts with nitrogen atoms, forming an amination reaction. The linker is covalently immobilized to the surface and the nature of this chemical is synthetic. 4-Nitrobenzylamine hydrochloride is synthesized by reacting nitric acid with benzaldehyde in ammonia solution at room temperature. This chemical has shown to be effective in reactions where a flow rate is needed or when diamidines are present in the reaction mixture.</p>

<p>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-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>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>Xylene cyanol is a chemical compound that belongs to the group of phenols. It has been shown to be active in vitro against human skin cancer cells, and induces cell lysis. Xylene cyanol has also been found to bind to the BCR-ABL kinase domain, which is an enzyme that plays a crucial role in the development of leukemia and other autoimmune diseases. Xylene cyanol binds to dna binding domains on the protein surface and forms an adduct with bcr-abl kinase, which inhibits its activity. This inhibition prevents activation of this enzyme and leads to cell death by preventing DNA synthesis.</p>

<p>4-Cyano-2-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>4-Amino-3-nitrobenzonitrile is an organic compound that is used as a precursor in the synthesis of drugs to treat infectious diseases. 4-Amino-3-nitrobenzonitrile has been shown to have potent activity against Leishmania species, including L. major and L. braziliensis. It binds to sulfoxides by a nitro group and forms a covalent bond with the sulfoxide. This results in the formation of an intramolecular hydrogen bond between the nitro group and the sulfoxide, which prevents it from forming hydrogen bonds with other molecules. Gel permeation chromatography can be used for analytical determination of this drug. 4-Amino-3-nitrobenzonitrile has also been studied using chemosensors and in vivo studies, showing that it can be used to inhibit protozoa such as Giardia lamblia, Entamoeba histolyt</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>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>3-Cyanopropionaldehydedimethylacetal (3CPDMA) is a reactive compound that inhibits the proliferation of muscle cells. It has been shown to inhibit the synthesis of 3-hydroxy-3-methylglutaryl coenzyme A, which is required for the production of cholesterol and fatty acids. This inhibition leads to a decrease in the growth of cells and their ability to divide. 3CPDMA has also been shown to have an inhibitory effect on picolinic acid, which is involved in the activation of receptors that induce cellular proliferation. The inhibition of this receptor may be due to its ability to compete with other ligands for binding sites on the receptor.<br>It has been shown that 3CPDMA acts as an antagonist against acarids, which are mites that feed on skin cells. This property may be due to its antagonistic effects on amino acid composition, which may affect calcium uptake by cells or cell membrane permeability.</p>

<p>4-Cyano-4'-aminobiphenyl is a fluorescent dye that exhibits a strong fluorescence under UV irradiation. The dye has an absorption maximum at about 335 nm and a fluorescence emission maximum at about 455 nm, with excitation maxima of 333 nm and 478 nm. It has been used in the development of photocurrent devices, which are used for photochemical reactions and electrochemistry studies. This compound can also be used for the determination of amino groups in organic molecules such as carbostyril. The compound can be synthesized by reacting an amine with an aldehyde in the presence of acid.</p>

<p>Please enquire for more information about 2-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>2-Cyano-3-fluoro-4-bromo aniline is a plant growth regulator that can be used to prevent and control the spread of viral diseases in plants. 2-Cyano-3-fluoro-4-bromo aniline inhibits the replication of influenza virus strains by binding to the viral coat protein. It also has been shown to inhibit proteolytic enzymes when applied as a coating on particles. The main mechanism of this compound is through its ability to bind to regulatory proteins, which prevents them from binding with other regulatory proteins and activating transcription factors. The expression profile suggests that this compound may regulate the expression of genes involved in plant development, cell division, and response to stress.</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>

<p>Please enquire for more information about 2-(Diphenylamino)benzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>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>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>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>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>5-Methoxyindole-3-acetonitrile is a synthetic compound used as a reference for the synthesis of melatonin. It is produced by the addition of magnesium to 5-methoxyindole, followed by reaction with cyanide and nitrile. The synthesis of this compound was first published in 1938 and has since been used as a reference for many other studies. It has been shown that 5-methoxyindole-3-acetonitrile has high performance liquid chromatography properties, with a linear range from 0.5 to 50 mg/mL and an ultraviolet spectrum that falls within the region between 220 nm and 400 nm. A molecular modeling study was conducted on this compound, which showed that it conforms with 4-hydroxy indole ring systems found in natural products such as tryptophan and serotonin. This product also has fluorescent properties, which are caused by its electron withdrawing group (cyano).</p>

<p>2-Chloro-5-cyanopyrazine is a synthetic compound that has been shown to have anti-cancer properties. It is an acceptor molecule that has a nucleophilic character and can react with electrophiles to form covalent bonds. This compound has been shown to selectively inhibit the growth of cancer cells in vitro. The mechanism of action is not yet clear, but it may be due to its ability to induce apoptosis and arrest cell cycle progression at the G1 phase. 2-Chloro-5-cyanopyrazine also has the potential for use as an analytical reagent because of its high solubility in organic solvents. In addition, this compound can be used as a copper donor in reactions involving carboxylic acids or other nucleophiles. <br>2-Chloro-5-cyanopyrazine can be synthesized from benzene and chloropicrin in the presence of copper(II)</p>

<p>4-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>