Heterociclos con oxígeno (O)

2-Propylfuran is a derivative of furan. It has been observed using a spectrometer that the compound reacts with alginic acid and β-unsaturated aldehydes to form disaccharides. 2-Propylfuran undergoes thermolysis to produce furfural, which is used in the production of certain foods. Furfural also has various health effects, including acting as an antioxidant, mutagen, and carcinogen. 2-Propylfuran may react with water molecules to produce hydrogen peroxide and hydroxyl radicals. It also reacts with aliphatic hydrocarbons to produce β-unsaturated ketones. 2-Propylfuran can react with halogens or other compounds to form a variety of products including alkyl halides, alcohols, amines, haloalkenes, amides, esters, nitriles, nitrosamines, and carboxylic acids.

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3,4-Epoxytetrahydrofuran is an organic compound with the chemical formula C8H8O2. It is a cyclic ether that can be synthesized by the reaction of epichlorohydrin and propylene oxide. The compound has two stereoisomers (R and S) due to the chiral nature of the propylene oxide starting material. 3,4-Epoxytetrahydrofuran is used in the production of acrylonitrile, which is used in the production of plastics. 3,4-Epoxytetrahydrofuran has been shown to have strong inhibitory effects on fungus Penicillium rubrum. This compound also inhibits germination rates in some plants.

6-Hydroxybenzofuran is a prenylated aromatic compound that has been shown to inhibit the activity of dopamine-beta-hydroxylase, an enzyme involved in the synthesis of norepinephrine and epinephrine. The chemical structure of 6-hydroxybenzofuran includes an amino group, a benzene ring and a hydroxyl group. Binding studies have shown that 6-hydroxybenzofuran has an affinity for amino transferases. It also inhibits the enzyme PTP1B, which is involved in the regulation of insulin secretion. In addition, 6-hydroxydbenzofuran has been found to cause neuroprotection by inhibiting the uptake of dopamine into brain cells and reducing oxidative stress.

(2-Butyl-5-nitro-3-benzofuranyl)[4-[3-(dibutylamino)propoxy]phenyl]methanone is a versatile compound that has multiple applications in various fields. It can act as a fluorescent probe for dopamine and other neurotransmitters, making it useful for neurochemical research. Additionally, it has been shown to inhibit the production of tumor necrosis factor-alpha (TNF-α), which is involved in inflammatory processes. This compound is commonly used as a research chemical due to its unique properties. It exhibits esterase activity, making it valuable for studying enzyme kinetics and drug metabolism. Furthermore, it has been used in studies involving trastuzumab, a monoclonal antibody used in cancer treatment, to investigate its pharmacokinetics and plasma levels. The heterocyclic structure of this compound makes it suitable for applications involving electrode materials. It can be incorporated into silicon oxide films or ceramic compositions to enhance their electrical

6-Methoxybenzofuran is a scalable, environmentally friendly and optimized process for the production of 2-hydroxy-4-methoxybenzaldehyde anhydride. The reaction is carried out using chloroacetic acid and chloroacetic anhydride to produce 6-methoxybenzofuran. This compound can be demethylated with sodium methoxide to produce 2-methoxybenzaldehyde, which can be used in the synthesis of other compounds.

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7-Methoxybenzofuran is a benzofuran derivative that has been shown to inhibit phosphodiesterase type 4 (PDE4) and PDE5, which are enzymes involved in the breakdown of cyclic nucleotides. 7-Methoxybenzofuran has potent inhibitor effects on these enzymes, especially at high concentrations. It is possible that this compound may be used as a treatment for asthma since it inhibits the production of inflammatory agents from cells. 7-Methoxybenzofuran has also been shown to have anti-inflammatory properties in animal models. This may be due to its ability to inhibit prostaglandin synthesis by inhibiting phosphodiesterase activity.

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Methyl-5-chloromethyl-2-furancarboxylate is an organic compound that belongs to the class of benzyl ethers. It is a colorless liquid with a strong, unpleasant odor. Methyl-5-chloromethyl-2-furancarboxylate has been shown to be an antiplatelet agent and to inhibit calcium ion influx into platelets, which leads to inhibition of platelet aggregation. It also has sulfhydryl properties and can be used as an antidote for sulfide poisoning. Methyl 5 chloromethyl 2 furancarboxylate is also used in the synthesis of other compounds such as methyl 5 chloromethyl 3 phenoxymethyl 2 furancarboxylate, methyl 5 chloromethyl 4 phenoxymethyl 2 furancarboxylate, and methyl 5 chloromethyl 3 methanethiol 1 furancarboxylate.

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