Heterociclos con oxígeno (O)

Please enquire for more information about N-(4-Aminophenyl)-1-benzofuran-2-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Iododibenzofuran is a class of activated aromatic molecules that react with triisobutyrate to form a fluorescent acceptor. 4-Iododibenzofuran has been used in devices that emit light at room temperature and can be modified by various substituents. These modifications allow for emission at different wavelengths, which makes it useful as an emitter. Thallium is often used as an activator to increase the efficiency of the molecule.

5-Bromofuran-2-yl)methanol is a triazole derivative that is synthesized via multicomponent reactions. It has been shown to be a high yield, functionalized, and sequence selective synthesis of triazoles. The synthesis of 5-bromofuran-2-yl)methanol can be achieved by the reaction of azide with (5-bromo-2-methylphenyl)methanol in dichloromethane solution. This process yields a high yield of the desired product with little side products.

Please enquire for more information about 6-Amino-4-methoxy-1-(2-deoxy-beta-D-ribofuranosyl)-1H-pyrazolo[3,4-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 Furan-2-carboximidamide hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

2'-Trifluoromethane sulfonate-2,3'-anhydro-1-(beta-D-xylofuranosyl)uracil is a nucleophile that hydrolyzes to form uracil. It can also be used as a linker in the formation of hexamethylphosphoric chloride and triamide derivatives.

Applications 5-HYDROXY-4-PROPYL-5H-FURAN-2-ONE (cas# 78920-10-2) is a useful research chemical.

Please enquire for more information about 5-Sulfo-2-furancarboxylicacid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Dibenzo[b,d]furan-2-carboxylic acid is a photophysical acid that has acidic properties. It is soluble in water and can be used as a cavity acid. Dibenzo[b,d]furan-2-carboxylic acid has been shown to have a strong enhancement effect on the fluorescence of aromatic carboxylate compounds by intermolecular hydrogen bonding. This compound also inhibits the growth of bacterial cultures by binding to their active site, which is a hydroxyl group. The nmr spectra of dibenzo[b,d]furan-2-carboxylic acid show that it has a naphthalene structure with two hydrogen atoms. Binding constants have been determined for this molecule with different compounds in order to study its binding affinity.

Please enquire for more information about 1-Tetrahydrofuran-2-ylethanamine 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-[(Methylamino)methyl]-2-furanmethanol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about N-(4-Amino-2-methoxyphenyl)-1-benzofuran-2-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about N-[(Z)-Amino(2,4-dioxodihydrofuran-3(2H)-ylidene)methyl]benzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about (E)-1-Benzofuran-2-yl(phenyl)methanone oxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

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);