Heterocycles with Oxygen (O)

2-Ethylbenzofuran is a benzofuran derivative that has been shown to be a potent inhibitor of acid transport. It is effective in the treatment of gastric and duodenal ulcers, as well as hyperchloremic acidosis. 2-Ethylbenzofuran inhibits the action of calcium carbonate by binding to the active site on rat liver microsomes. This binding prevents the formation of an enzyme-inhibitor complex with polyvinyl chloride, which is required for dibutyl acylation reaction and acidolysis. The drug also blocks acid transporter activity, which may be due to its ability to induce demethylation and inhibit calcium carbonate from forming an enzyme-inhibitor complex with polyvinyl chloride.

Applications 2-(Furan-2-yl)-2-(methoxyimino)acetic Acid is an intermediate in the synthesis of Cephalosporin derivatives.
References Ger. Offen. (1978), DE 2731724 A1 19780119.

Applications Tetrahydro-2-furanmethanamine is used in the synthesis of novel topoisomerase I targeting anti-cancer agents with mild to potent cytotoxic activity. Also used in the discovery and synthesis of orally bioavailable stearoyl-CoA desaturase 1 inhibitors
References Lopez-Rodriguez, M. et al.: 44, 4504 (2001); Liu, G. et al.: J. Med. Chem., 50, 3086 (2007);

Applications 2,3,5-Trimethylfuran (cas# 10504-04-8) is a useful research chemical.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

Applications 6-Amino-5-(1,1-dimethylethyl)-3,3-dimethyl-2(3H)-benzofuranone is an intermediate in synthesizing Ivacaftor Carboxylic Acid (I940605). It is an impurity of Ivacaftor (I940600); a drug used in the treatment of cystic fibrosis.
References Clancy, J. et al.: Am. J. Resp. Crit. Care. Med., 186, 593 (2012)

Applications 2,5-DIMETHOXYTETRAHYDROFURAN (cas# 696-59-3) is a useful research chemical.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

Applications (R)-5-Oxotetrahydrofuran-2-carboxylic Acid is an intermediate used to synthesize 2',3'-dideoxy-4'-selenonucleosides as potential antiviral agents.
References Jeong, L., et al.: Bioorg. Med. Chem., 16, 9891 (2008)

Applications Used in the preparation of D-xylofuranose derivatives.

Applications (R)-2-(Benzyloxy)-5-((5-oxotetrahydrofuran-2-yl)methyl)phenyl Neopentyl Sulfate is an intermediate in the synthesis of metabolite of (-)-Epicatechin (E582260).

Applications 5-(1,1-Dimethylethyl)-3,3-dimethyl-6-nitro-2(3H)-benzofuranone is an intermediate in synthesizing Ivacaftor Carboxylic Acid (I940605). It is an impurity of Ivacaftor (I940600); a drug used in the treatment of cystic fibrosis.
References Clancy, J. et al.: Am. J. Resp. Crit. Care. Med., 186, 593 (2012)

Applications 2-Cyano-N-((furan-2-ylmethyl)carbamoyl)acetamide is an intermediate in the synthesis of novel 1- and 8-substituted-3-furfuryl xanthines as adenosine receptor antagonists.
References Balo, M. C., et al.: Bioorg. Med. Chem., 17, 6755 (2009);

Applications Methyl 4-Bromofuran-2-carboxylate is used to prepare pyrimidinamines and pyridinamines as adenosine receptor modulators for treatment of CNS disorders.
References Borroni, E., et al.; PCT Int. Appl., WO 2001062233 A2 20010830 (2001)

Applications Intermediate in the production of Bufuralol Hydrochloride

5-Formylfuran-2-boronic acid is a compound that has been shown to be used in the synthesis of Pd complexes. This compound was found to inhibit the soluble guanylate cyclase and sirtuin 2 enzyme. It also has been shown to have anti-cancer effects, as it may inhibit cancer cell proliferation. 5-Formylfuran-2-boronic acid has been shown to increase the transport properties of potassium dichromate, which may be due to its acidic nature. This red fluorescent compound is soluble in organic solvents and can be activated by light. The optimum concentration of 5-Formylfuran-2-boronic acid is 3 mM in an acidic solution at room temperature.

5-Ethoxy-2(5H)-furanone is an oxidation product of 5-ethoxy-2(5H)-furanone. It has an isomeric, stereospecific, regiospecifically, and a tautomeric relationship with furfural. 5-Ethoxy-2(5H)-furanone can be produced by the oxidation of furfural with boron trifluoride etherate in the presence of iodosobenzene. The reaction mechanism involves the addition of hydrogen peroxide to the boron trifluoride etherate to form hydroperoxydiborane. This compound then reacts with iodosobenzene to produce 5-ethoxy-2(5H)-furanone and 2,5-dihydroxybenzaldehyde. The reaction produces a mixture of diastereomers that contain different numbers of carbon atoms due to the regiospecific

M02322 - Parthenolide

M02705 - 5-Bromo-3-indolyl-b-D-galactopyranoside

Please enquire for more information about methyl 5-(((4-chlorophenyl)sulfonyl)methyl)furan-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Ethyl-4-hydroxy-2-methyl-3(2H)-furanone is a colorless liquid that has a fruity, sweet odor. It is used in the manufacture of flavors and fragrances. 5-Ethyl-4-hydroxy-2-methyl-3(2H)-furanone can be obtained by the reaction of butanedione with dilute sulfuric acid, followed by treatment with an absorber containing propylene glycol and 4-ethyl-2methoxyphenol. The product is then treated with radiation energy to produce furfural, which reacts with anthranilate to form methyl anthranilate. Methyl anthranilate can be converted into phenylmethyl by reacting it with glycosidase.

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

Applications 3-Furanmethanol (cas# 4412-91-3) is a useful research chemical.

Applications 5-Nitro-1-benzofuran is a chemical reagent used in the synthesis of internal alkynes. Also used in the preparation of anti-oxidants quinolines.
References Lu, L. et al.: Eur. J. Org. Chem., 2013, 1644 (2013); Kuzmin, V. et al.: Russ. Chem. Bull., 57, 2405 (2008);

Applications (2S,3S,4R,5R)-2-(6-Amino-9H-purin-9-yl)-5-(((3-aminophenyl)thio)methyl)tetrahydrofuran-3,4-diol is an enantiomer of (2R,3R,4S,5S)-2-(6-Amino-9H-purin-9-yl)-5-(((3-aminophenyl)thio)methyl)tetrahydrofuran-3,4-diol (A577286), which an intermediate used in the synthesis of S-adenosylhomocysteine analogs with biological activities.
References Lawrence, F., et al.: Biochem. S-Adenosylmethionine Relat. Compd., Proc. Conf., 637 (1982); Shire, D., et al.: Nucleosides & Nucleotides, 2, 21 (1983)

Applications Furan-2-boronic acid