Heterociclos con azufre (S)

Please enquire for more information about 2-Amino-4-(4-butylphenyl)thiophene-3-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 5-Fluoro-1-[(2R,5S)-2-(Hydroxymethyl)-1,3-Oxathiolan-5-Yl]Pyrimidine-2,4-Dione including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 3-Amino-N-methylthiophene-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 Ethyl 2-amino-4-(1,1'-biphenyl-4-yl)thiophene-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 2-Amino-N-(2-methoxyphenyl)-6-methyl-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

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

Ethyl 5-amino-4-cyano-3-(2-ethoxy-2-oxoethyl)thiophene-2-carboxylate is a white crystalline powder. It is soluble in organic solvents, alkali metals and sulfates, and has high solubility in citric acid at room temperature. It is also soluble in magnesium sulfate and acetonitrile, but insoluble in water. The solubilities of ethyl 5-amino-4-cyano-3-(2-ethoxy -2 -oxoethyl)thiophene -2 -carboxylate are dependent on the pH of the solution. The melting point of this compound is 207° C, with a boiling point of 242° C. This compound can be thermodynamically modelled using HSCIAMMO software and correlated to experimental data for solubility. Ethyl 5 amino 4 cyano 3 (2 eth

Please enquire for more information about 4,5-Dihydrothieno[2,3-e][1]benzothiophene-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-Ethyl 4-isopropyl 5-amino-3-methylthiophene-2,4-dicarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Bromothiophene-2-sulfonamide is a cationic surfactant that is used in detergents, shampoos, and bath oils. It is also an antibacterial agent that kills bacteria by disrupting the lipid bilayer membrane of the cell wall. 5-Bromothiophene-2-sulfonamide has been shown to have potent inhibitory effects on the growth of Gram-positive and Gram-negative bacteria such as Staphylococcus aureus, Escherichia coli, Salmonella typhi, Pseudomonas aeruginosa, Klebsiella pneumoniae, and Acinetobacter baumannii. This compound has also been shown to have constant inhibitory properties against all bacterial strains tested.

Please enquire for more information about 2-Amino-5-methyl-4-phenyl-N-(pyridin-3-ylmethyl)thiophene-3-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-tert-Butylthiophenol is a colorless liquid that binds to hydroxyl groups and can be used as an inhibitor of metabolic reactions. It is a nonpolar solvent with a boiling point of 101°C. 4-tert-Butylthiophenol has been shown to inhibit the growth of bacteria in primary culture. The functional theory for 4-tert-butylthiophenol's binding to bacterial DNA is that it forms hydrogen bonds with the phosphate backbone and may also react with the hydroxyl group on the sugar molecules. The functional groups present in this compound are an alkynyl group and a hydroxyl group, both of which are nonpolar and therefore soluble in nonpolar solvents such as chloroform and benzene. 4-tert-Butylthiophenol also reacts with nucleic acids through transfer reactions, which are chemical reactions where one or more electrons are transferred from one atom

2-Bromo-4-hexylthiophene is a monomer that is used in the production of polymers, plastics, and solar cells. It has been synthesized experimentally as well as theoretically. The yield of this chemical reaction can be improved by using the cross-coupling technique or isomerization. 2-Bromo-4-hexylthiophene does not have an optical activity and it can be used for the synthesis of low molecular weight heterocycles. This chemical has been shown to terminate polymers with an amine group on one end and a phenothiazine group on the other end, which are then used for solar cell devices.

Please enquire for more information about 3-Chloro-6-nitro-1-benzothiophene-2-carbohydrazide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Thiophene-3-carbaldehyde oxime including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 4,5,6,7-Tetrahydro-1-benzothiophene-2-carbonyl chloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Iodo-2-thiophenecarbonitrile, also known as 5-iodo-2-benzothiophene, is a benzothiophene that has been dehydrated to form a five-membered singlet. This compound is used as a transient and has yielded high yields of furan in a photocleavage reaction. 5-Iodo-2-thiophenecarbonitrile can be synthesized from methylcyclohexane with the use of Wittig reactions. It is also a good sensitizer for photochemical reactions due to its nucleophilic nature.

Please enquire for more information about 5-Methyl-4-phenylthiophene-3-carbohydrazide including the price, delivery time and more detailed product information at the technical inquiry form on this page