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Furan-2-yl-triMethyl-silane is a synthetic compound that contains a carbonyl group and three methyl substituents. It reacts with dichlorocarbene to form a furyl compound in the presence of a phosphonium salt or silicon. Furan-2-yl-triMethyl-silane can also react with lithium species to form an alkyl compound, which can be irradiated to produce an alkylation product. The regiospecificity of this reaction depends on the type of alkyl group used. Furan-2-yl-triMethyl-silane has been used in the production of photosensitized polymerization reactions and photoelectron spectroscopy.

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Applications Methyl 5-bromofuran-2-carboxylate

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(S)-4,4,7a-Trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one is a natural product that has been studied as a model system for the biosynthesis of dihydroactinidiolide. It is also a substrate for carotenoid biosynthesis and has been shown to inhibit the activities of various enzymes involved in neuronal death. It is also genotoxic and has been shown to induce apoptosis in various cell lines such as neuro2a cells and carcinoma cell lines.

2-Methylbenzofuran is a benzofuran derivative that inhibits the reaction mechanism of carbofuran, which is an insecticide. 2-Methylbenzofuran reacts with the hydroxyl group of carbofuran to form a reactive intermediate. The aromatic hydrocarbon is then converted to the corresponding benzene derivative by chromatographic science and 13C NMR spectroscopy. Phase equilibrium and chemical analyses are used to determine the purity of the product, while recycled 2-methylbenzofuran can be synthesized from fatty acids. The analytical method for this compound is a Friedel-Crafts reaction, which entails reacting 2-methylbenzofuran with phenylhydrazine in refluxing ethanol.

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Applications cis-2,5-Dimethyltetrahydrofuran is a byproduct of the catalytic conversion of sugars and polyols to biomass-derived carbohydrates. Dihydrofuranyl derivative. References West, R. et al.: Catalysis Today., 147, 115 (2009);

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(1-Benzofuran-2-ylmethyl)amine hydrochloride is an aliphatic hydrocarbon that is used as a pharmaceutical preparation. It has been shown to be active against autoimmune diseases such as rheumatoid arthritis and multiple sclerosis, and it also has activity against neurological disorders. (1-Benzofuran-2-ylmethyl)amine hydrochloride is synthesized by reacting phenylsulfonyl chloride with the amine. The asymmetric synthesis of this compound results in two different enantiomers that are mirror images of each other. One of these enantiomers, called (+)-(1-benzofuran-2-ylmethyl)amine, has been shown to be active against depression and psychosis. The other enantiomer is inactive.

2-Bromo-1-furan-2-yl-ethanone is a colorless liquid that is soluble in organic solvents. It has been shown to possess the ability to form a variety of chemical bonds with molybdenum, copper, and other elements. The compound is used as a starting material for synthesis of natural products and pharmaceuticals. 2-Bromo-1-furan-2-yl-ethanone was first synthesized by the reaction between an aldehyde and methyl bromide in methanol solvent. This same reaction can be catalyzed by copper(I) iodide or iron(III) chloride. Cytometry has revealed that this compound's basic structure adopts two conformations: one with the furan ring flipped over, and one with the furan ring lying flat on the plane of the molecule. This molecule also possesses enantioselective properties, which are due to its chiral center

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2-(Benzofuran-3-yl)ethanamine (ZBFEA) is a novel synthetic derivative of the natural product 2-(benzofuran-2-yl)ethanamine. It has been shown to be effective against multiresistant bacteria such as Staphylococcus aureus, including methicillin resistant strains. ZBFEA inhibits bacterial growth by binding to the ribosomal protein S12 and preventing protein synthesis. This compound has also been shown to have fluorescent properties, which may be useful for its use as a diagnostic agent in live bacterial cultures.

Applications 2-(5-formylfuran-2-yl)benzoic Acid (cas# 88460-72-4) is a useful research chemical.

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Nilotinib is a small molecule that inhibits the tyrosine kinase activity of TK1, TK2, and TK3. It binds to the ATP-binding site of these kinases and prevents the phosphorylation of the cellular substrate. Nilotinib has been shown to inhibit the proliferation of leukemia cells in vitro, as well as to have antiproliferative effects in vivo. Nilotinib can be used for the treatment of chronic myelogenous leukemia (CML) and Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL). In addition, it has been shown to have synergistic effects with other drugs such as α1-acid glycoprotein inhibitors or methyltransferase inhibitors. Nilotinib can also be used for cases of hepatic steatosis.

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3-Bromobenzofuran is an organic compound with a chemical formula of C8H6BrO. It has been used in the synthesis of several pharmaceuticals, including clopidogrel and ticagrelor. The elimination reactions of 3-bromobenzofuran have been extensively studied, which involve protonation, boronic acid addition, and nucleophilic substitution. Kinetic studies have shown that the reaction rate is dependent on the functional group present on 3-bromobenzofuran. The skeleton of 3-bromobenzofuran can be modified to produce aryl boronic acids or carbinols through a palladium-catalyzed coupling reaction with an aryl halide or chloride. This process can also be reversed to synthesize benzofurans from the corresponding aryl boronic acids or carbinols.

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3,6-Dimethyl-4,5,6,7-tetrahydro-1-benzofuran is a monoterpene that has been shown to have antimicrobial activity against a wide range of microorganisms. It is a reactive compound and reacts with the thiol groups of proteins and other thiols in the cell. This reaction inhibits transcriptional regulation and protein synthesis by binding to the target enzymes. 3,6-Dimethyl-4,5,6,7-tetrahydro-1-benzofuran has been shown to inhibit photosynthetic activity in plants as well as the growth of fungi in vitro.