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5-Methyl-2-furancarbonylchloride (5MFCC) is a chlorinating agent that is used in organic synthesis. It is often used as a diluent for hydrogen chloride and density lipoprotein cholesterol. 5MFCC reacts with thionyl chloride to produce pentose phosphate, which is converted to aldehydes, such as acetaldehyde or benzaldehyde. These aldehydes are further reacted with lipoproteins to form activated lipid profiles. Activated lipid profiles are used in the detection of various diseases, such as atherosclerosis and diabetes mellitus.

Please enquire for more information about 1-(2,3,5-Tri-O-benzoyl-2-C-beta-methyl-beta-D-ribofuranosyl)-5-nitropyridine-2(1H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 6-Bromobenzofuran-2-carboxylicacid including the price, delivery time and more detailed product information at the technical inquiry form on this page

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

Please enquire for more information about Methylbenzofuran-2-acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,5-Dihydrofuran is a reactive organic molecule that contains two hydrogens and two carbon atoms. The optimal energy for the reaction of 2,5-dihydrofurans with hydrogen fluoride is low, which makes it a good reactant in acid conditions. 2,5-Dihydrofuran has been shown to be an intermediate in the formation of ethyne by transfer reactions. The histological analysis of cells treated with 1% 2,5-dihydrofuran showed a decrease in the number of cells with an intact nucleus. The isotopomer distribution data revealed that the concentration of 2,5-dihydrofurans increased after treatment with hydrogen fluoride. These results suggest that 2,5-dihydrofurans are formed by the reaction between hydrogen fluoride and ethyne.

Please enquire for more information about 4-Chloro-5-fluoro-7-(2-deoxy-beta-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 5-Nitro-2-[(tetrahydrofuran-2-ylmethyl)amino]benzonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

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3-Methyl-2-nitrofuran is a nitro compound that has been shown to undergo photoinduced electron transfer reactions. It is produced by the rearrangement of dihydropyridines and has been used as an intermediate for the synthesis of other nitro compounds. 3-Methyl-2-nitrofuran is an example of a nitro compound, which has been demonstrated to undergo photoreactions and acetonitrile chemistry. The mechanism for this reaction is not completely understood, but it may involve the formation of a nitrite ion by electron transfer from the methyl radical on one molecule to another molecule. This reaction produces a radical cation with two unpaired electrons, which then reacts with acetonitrile to form a nitroalkene.

Furan-2-carbothioamide is a chemical compound that has been analysed. It is a mesylate salt that can be found in nature. Furan-2-carbothioamide will react with chloride to yield an aqueous solution of hydrochloric acid and nitrite. Furan-2-carbothioamide has been used as a reagent for the formylation of dipole solutes and the hydrolysis of nitro compounds. Furan-2-carbothioamide is also very soluble in benzene and reacts with solvents such as hydrochloric acid, nitric acid, or sulfuric acid.

Please enquire for more information about 1-(Tetrahydro-2-furanylmethyl)-1H-pyrrole-2-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Tetrahydrofuran-2-ylpropanoic acid is a gas sensor that has been shown to be sensitive to the presence of chloride, water vapor, and hydrogen sulfide. It is used in particle detection and has a fluorescence probe for Cd(II). The quantum yield for 3-tetrahydrofuran-2-ylpropanoic acid was found to be 0.3%. 3-Tetrahydrofuran-2-ylpropanoic acid has an affinity for peroxidase activity and can be used as a low energy hydrogen bond donor. This compound also shows synergistic effects with microspheres.