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Please enquire for more information about (3aR,4R,5R,6aS)-4-[3-(Ethyleneketal)decanyl]hexahydro-5-hydroxy-2H-cyclopenta[b]furan-2-one 5-(4-phenylbenzoate) including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Aminotetrahydrofuran is an organic compound that has inhibitory activity against a wide range of microorganisms. 3-Aminotetrahydrofuran is synthesised by reacting ethyl ester with nitrochloride in the presence of magnesium and hydrochloric acid. The chloride ion is also added to this reaction, which allows for the synthesis of quaternary ammonium salts. 3-Aminotetrahydrofuran inhibits protein synthesis by inhibiting c1-4 alkyl transfer reactions, which are required for the synthesis of proteins. It also inhibits hydroxyl group transfer reactions, which are needed for the production of ribosomes and many other cellular components.

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Applications 2,5-Dihydrofuran is used in the synthesis of Sch 38516 aglycon (fluvirucin B1) an influenza A antibiotic. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Tomita, K. et al.: J. Antibiot., 44, 940 (1991); Houri, A. et al.: J. Am. Chem. Soc., 117, 2943 (1995);

Applications 7-Bromo-1-benzofuran Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

3,4-Dichlorophenylmagnesium bromide - 0.5M solution in tetrahydrofuran is a chemical reagent that is used to produce methyl compounds. It is often used in the production of chlorinated compounds by substitution of chlorine atoms for hydrogen atoms on the carbon chain. 3,4-Dichlorophenylmagnesium bromide - 0.5M solution in tetrahydrofuran has a molecular structure that includes an electronegative chloro group and a titanium ligand. Acid catalysts are often used with this chemical to promote the reaction between the magnesium and halide ions, which produces methylation products. This may be done through x-ray analysis to determine the progress of the reaction.

2-Butyl-5-nitrobenzofuran (2B5NBF) is a drug that belongs to the class of salicylaldehydes. It is an acylation product of 2-butanol and 5-nitrobenzofuran that has the potential for use as a pharmaceutical agent. The reaction yield for this compound is high and can be increased by using hydrochloric acid as the acid catalyst. When 2B5NBF is reacted with chloride, it produces an active substance with a structural formula of C14H11NO3Cl. This substance has been shown to have arrhythmic properties in atrial tissue in rats.

Benzofuran is a coumarin derivative that can be used as an antimicrobial agent. It has been shown to have reactive properties, which are due to the formation of a covalent bond between benzofuran and the target molecule. Benzofuran has been shown to inhibit the mitochondrial membrane potential and damage the papillary muscle in rats with congestive heart failure. This drug also binds to receptors in cells, affecting their activity and causing biological changes. The reaction solution is bound form, which is a form of benzofuran that does not react with other molecules and thus remains unchanged.

2,3-Dihydro-5-methyl-4-[(2-methyl-3-furanyl)dithio]furan (DMDF) is a novel drug that has been shown to inhibit the growth of human prostate cancer cells. DMDF also inhibits adipose cell growth and human osteoblast cell proliferation in vitro. It binds to sequences on the promoter region of genes that are responsible for the production of proteins involved in tumorigenesis, including growth factors and receptor tyrosine kinases. DMDF also binds to monoclonal antibodies against the alkylthio group of DNA, which may be an important factor in its antitumor activity.

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