Cyano-, Nitrile-

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2-Cyano-2-(hydroxyimino)acetamide is a reactive oxime that can be used as a reagent to synthesize peptides. It is used in the synthesis of peptides with high efficiency and has been shown to be an effective reagent for the synthesis of peptides containing an N-terminal cysteine. 2-Cyano-2-(hydroxyimino)acetamide is used in the preparation of 1-hydroxy-7-azabenzotriazole, a carbodiimide. The product is also used as an additive in pharmaceutical preparations to increase their stability by preventing hydrolysis and oxidation.

Applications Methyl 4-Cyanobenzoate (cas# 1129-35-7) is a compound useful in organic synthesis.

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. 2-Acetoxybenzonitrile binds metal cations such as Cu(II), Fe(

Ethyl 3,3-Bis(methylthio)-2-cyanoacrylate is a reactive compound that can be used to form esters and amides. The synthesis of this compound is achieved by reacting sodium sulfide with anhydrous potassium carbonate in the presence of ethyl 2-cyanoacrylate. This reaction forms a thermally stable ester of ethyl 3,3-bis(methylthio)-2-cyanoacrylate. Ethyl 3,3-Bis(methylthio)-2-cyanoacrylate is a nucleophilic reagent that reacts with pyrazole derivatives to form amides. The diffraction data for this compound was obtained using single crystal x-ray diffraction techniques.

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

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. !-- END OF PRODUCT DESCRIPTION -->

Cyanomethylenetributylphosphorane (CMTP) is an agent used for the diagnosis of body formation. It is a chemical compound that can be used to produce images of tissue and organs by detecting apoptosis, or programmed cell death. CMTP binds to the glucose-dependent insulinotropic polypeptide receptor (GIPR), stimulating the release of insulin in the pancreas. CMTP also has therapeutic potential for metabolic disorders, as it has been shown to reduce triglycerides and increase HDL cholesterol levels in human serum. CMTP is synthesized from trifluoroacetic acid, which is then reacted with a cyclic peptide containing an amino acid derivative and 1-methyl-2-pyrrolidinone. This reaction produces a molecule with one free amino group at one end and two free carboxylic acid groups at the other end. The molecule can be reacted with epidermal growth factor (EGF) or insulin to

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1,6-Bis(cyano-guanidino)hexane is a bactericidal agent that can be used to remove bacteria from water. The compound has been shown to have a bactericidal activity against Gram-positive and Gram-negative bacteria in concentrations of 100 mg/L and 200 mg/L, respectively. 1,6-Bis(cyano-guanidino)hexane has also been shown to be effective against industrial strains of Bacillus subtilis and Pseudomonas aeruginosa in concentrations of 200 mg/L. This compound is soluble in organic solvents but insoluble in deionized water. It has a viscosity of 30000 cP at 20°C and an anion charge of -1.

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2-[2-Fluoro-4-(trifluoromethyl)phenyl]acetonitrile is a trimeric impurity found in the synthesis of cefepime. It is a reactive compound that can form adducts with trimethylamine, thiols, and amines.

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Potassium cyanoacetate is an organic compound that is used in the synthesis of pharmaceuticals. It is a potential precursor for the preparation of many drugs, including anti-inflammatory agents, anti-epileptics, and anti-cancer drugs. Potassium cyanoacetate is a good reagent for cross-coupling reactions because it reacts efficiently with methyl alcohol, cycloaliphatic compounds, and aromatic chlorides to produce functionalized products. The potassium salt can be obtained from the reaction of cyanamide with potassium hydroxide in an organic solvent at room temperature. Potassium cyanoacetate has been used as a linker in the synthesis of various drugs.

2-Methylbenzoylacetonitrile is a reactive compound that can undergo cyclization and oxidation reactions. It can be used in the synthesis of other compounds, such as acetophenone. The postulated mechanism of this reaction is shown below: 2-methylbenzoylacetonitrile + tert-butyl hydroperoxide → 2-methylbenzoic acid + tert-butyl alcohol + hydrogen peroxide 2-methylbenzoic acid + thiourea → 2-methylbenzoyl amide 2-methylbenzoyl amide + methylene → 2-(2-methylphenyl)acetamide Hydroperoxide (HOOH) + methylene → acetic acid This reaction forms an acetic acid molecule and a methylene molecule.

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2-Amino-3-cyano-4-hydroxythiophene is a pyridine that has been found to react with malononitrile and hydrosulfide in the presence of a catalytic amount of thiophene. The reaction system can be used for the synthesis of various isomers, such as 2-thioglycolic acid, which is an intermediate in the production of thioglycolic acid. The substance also reacts with ethanol to form methylate. 2-Amino-3-cyano-4-hydroxythiophene can be used as a building block for synthesizing thioglycolic acid, which is then converted into thioglycolates. This process may be useful for the synthesis of substances that are difficult to produce synthetically.

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2-Cyanobenzyl alcohol is a flavin-dependent oxidant that catalyzes the oxidation of carotenoids and oxygenated compounds. 2-Cyanobenzyl alcohol can be used to produce large quantities of paramylon, which can be converted into fuels or chemicals. 2-Cyanobenzyl alcohol is an isomer of benzyl alcohol, but it has a different function because it cannot be converted into a primary alcohol. 2-Cyanobenzyl alcohol is used as a ligand in biological research and it has functional groups that are important for physiological processes. 2-Cyanobenzyl Alcohol is also known as 4-(4'-hydroxyphenyl)butanal or 4-(4'-hydroxyphenyl)butyraldehyde.