Cyano-, Nitrile-

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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.

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.

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Pyridine-2-acetonitrile is an organic compound with the formula CH3CN. It has a fluorescence emission maximum at about 335 nm and a molar refractivity of 1.8. Pyridine-2-acetonitrile is an ester of pyridine and acetonitrile, which has a viscosity of 0.24 cP at 25 °C and a hydrochloric acid solubility of 3.1 g/100 mL (0.5 M). In addition, it reacts with chlorine to form chloroform, which is soluble in water and insoluble in ether or alcohols. Pyridine-2-acetonitrile is used as the starting material for the synthesis of coumarin derivatives and other compounds that contain nitrogen atoms, such as nucleophilic agents used in coordination chemistry. The quantum theory provides a more efficient method for predicting the properties of this compound than classical theories do.

Methyl isocyanoacetate (MIC) is a compound that has been shown to inhibit the production of inflammatory cytokines, such as interleukin-1β, tumor necrosis factor α, and IL-8. These compounds are important in the development of cancer and inflammatory diseases. MIC also inhibits serine protease activity and choroidal neovascularization in animal models. This drug also has anti-inflammatory effects on human tissue, which may be due to its ability to inhibit the production of prostaglandins by blocking the conversion of arachidonic acid into prostaglandin H2. The carbonyl group on MIC interacts with amines on proteins, preventing them from forming covalent bonds with other proteins.

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Applications A Wittig reagent. References Laine, D., et al.: J. Med. Chem., 52, 5241 (2009), Nakao, A., et al.: Bioorg. Med. Chem. Lett., 19, 4607 (2009), Arakawa, Y., et al.: Chem. Pharm. Bull., 57, 167 (2009),

Please enquire for more information about 6-Cyano-2-(4-cyanophenyl)indole including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Fluorouracil is a pyrimidine-based chemotherapy drug that inhibits DNA synthesis by inhibiting the activity of the enzyme thymidylate synthase, thereby preventing the production of thymine nucleotides. Fluorouracil is used to treat cancers such as colorectal cancer and breast cancer. It is also used as adjuvant therapy for head and neck cancer. Fluorouracil works by binding to the enzyme dihydrofolate reductase, which is required for the synthesis of DNA precursors. This binding prevents the formation of tetrahydrofolate, which is essential for cell division. The main side effects are myelosuppression and gastrointestinal toxicities, which can be reduced or prevented with appropriate doses (lowering dose) or discontinuation (in case of gastrointestinal toxicity).

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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.

3-Hydroxybenzylamine hydrochloride (3HBH) is a chemical compound that has been used as a reagent and in the synthesis of other compounds. It is also known to be a useful scaffold for complex compounds, and can be used as a building block for the synthesis of fine chemicals. 3HBH has been found to have many applications in research, such as being an intermediate for pharmaceuticals, pesticides, dyes, and agrochemicals. 3HBH is also useful in organic syntheses where it has been found to react with nitriles and amides to form esters and amides respectively.

Acetonitrile-D3 is a compound that contains a hydroxyl group and a nitrogen atom. It is used as a diagnostic agent in kinetic data, FT-IR spectroscopy, and chemical reactions. Acetonitrile-D3 has been shown to form stable complexes with acidic molecules such as phosphoric acid. The reaction mechanism for the formation of these complexes is not yet known. This compound can be used to measure the concentration of alcohols, amines, and nitro compounds in test samples. Acetonitrile-D3 also has a deuterium isotope effect on chemical reactions, which may be due to the strength of hydrogen bonds formed between the compound and other reactants.