Heterociclos con azufre (S)

Please enquire for more information about 5-(Trifluoromethyl)thiophene-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2-Amino-6-(1,1-dimethylpropyl)-N-(2-furylmethyl)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Phenylthiophenol is a phenolic compound that has the chemical formula C6H5C6H4OH. It reacts with borohydride to form phenylboronic acid, which can be used as a reagent in organic synthesis. 2-Phenylthiophenol is an electron-rich molecule and it can be used to study surface properties and reaction mechanisms. 2-Phenylthiophenol reacts with biphenyl to form monolayers on silicon dioxide surfaces. Some of its properties are affected by environmental factors, such as its reactivity towards methyl ethyl ketone and its ability to bind to carbonyl groups.

Please enquire for more information about 3-Amino-5-(2-methyl-2-propanyl)-2-thiophenecarbonitrile 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-Bromobenzo[b]thiophene-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Bromomethylthiophene is an organosulfur compound that is used in the cross-coupling reaction with phenylsulfonyl halides to produce terminal alkynes. It can also be used as a ligand for metal complexes, where it acts as a dipole and binds to the metal center by means of electron donation from its methylene group. 2-Bromomethylthiophene can be found in polyester resins, which are used in the production of film and paper. The bromine atom has been shown to bind to dopamine receptors, which may account for some of its biological activity. The optical properties of this molecule have been studied extensively and have shown that it displays strong absorption bands at wavelengths between 350 nm and 450 nm.

Applications Intermediate in the preparation of Rotigotine References Janssens, F., et al.: J. Med. Chem., 29, 2290 (1986),

Please enquire for more information about 5-(Methylthio)-4-phenyl-3-(1H-pyrrol-1-yl)-2-thiophenecarboxylicacid methylester including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Ethyl 2-amino-4-(4-isobutylphenyl)-5-methylthiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Ethyl 2-anilino-4-oxo-4,5-dihydrothiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications Dibenzothiophene-2-boronic acid is a useful reagent for organic synthesis and other chemical processes. References Duncton, M. A. J., et al.: Org. Lett., 10, 3259 (2008)

Benzo[b]thiophen-2-amine is a chromophore that has been synthesized to be used as a dyebath intermediate. It is an amine with two electron withdrawing groups at the 2 and 6 positions, which can interact with copper salts to produce a triflic acid. The dyebath intermediate can then be used in the synthesis of ruthenium complexes. In addition, benzo[b]thiophen-2-amine has been shown to have cytotoxic effects against tumor cells and is currently being investigated for its potential use as an anticancer drug.

Please enquire for more information about Ethyl 2-amino-5-propylthiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

7-Bromobenzothiophene is a chemical compound that can be used as a coupling reagent in organic chemistry. It has been shown to be effective in the synthesis of biologically active compounds, such as anilines and organolithium compounds. 7-Bromobenzothiophene is also able to react with acetonitrile to produce reactive intermediates which are able to form covalent bonds with nucleophiles. This is important for the synthesis of diverse molecules, such as pharmaceuticals, polymers, and fluorescent dyes. The mechanism of this reaction has been investigated using photophysical methods and found to involve ns5b polymerase. The polymerase molecule catalyzes the formation of RNA by using DNA as a template. 7-Bromobenzothiophene has also been shown to inhibit hepatitis C virus (HCV) replication, although it does not inhibit the virus itself.

Please enquire for more information about N-(4-Methylphenyl)-2,3-dihydrothiophen-3-amine 1,1-dioxide including the price, delivery time and more detailed product information at the technical inquiry form on this page