Hétérocycles soufrés (S)

Please enquire for more information about Ethyl 2-[(4-fluorophenyl)amino]-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

Please enquire for more information about 2-Amino-4-ethyl-5-methylthiophene-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-Ethylthiophene-3-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 tert-Butyl benzo[b]thiophen-2-ylcarbamate 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'-Bromo-2,2':5',2''-terthiophene 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-tert-butyl-N-(3-methylphenyl)-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 Isopropyl 2-amino-5-isopropylthiophene-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-6-ethyl-N-(4-methylphenyl)-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 5-Bromo-2,3-dichlorothiophene 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-Acetylphenyl)-4-ethyl-5-methylthiophene-3-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Bromothiophene-2-carbaldehyde is an organic compound that has been shown to have antibacterial activity. It can be synthesized by reacting triethyl orthoformate with methyl ketones in the presence of a photocatalyst such as titanium dioxide or zinc oxide. This reaction produces 3-bromothiophene-2-carboxylic acid which reacts with ammonia and hydrogen bromide to form 3-bromothiophene-2-carbaldehyde. 3-Bromothiophene-2-carbaldehyde has been shown to inhibit the growth of cancer cells and induce apoptosis, which may be due to its ability to inhibit angiogenesis. The anticancer properties are most likely due to its ability to bind DNA and inhibit protein synthesis, leading to cell death.

3-Aminoethylthiophene hydrochloride (3AET) is a small molecule that inhibits the PARP-1 enzyme, which is involved in DNA repair. 3AET is a potent inhibitor of the maleimide mutant, damaged endogenous and exogenous DNA. It has been shown to be orally active when polymerized into micelles for delivery to the nuclear compartment. The electrochemical properties of 3AET have been studied and found to be due to its ability to form carboxamides with amines from proteins such as histones and nucleic acids. 3AET also prevents the polymerization of dsDNA, which may be used for prevention of cancerous tumors.

Please enquire for more information about ethyl 2-amino-6-methyl-4,5,6,7-tetrahydro-1-benzothiophene-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 Isopropyl 2-amino-5-(aminocarbonyl)-4-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-[(chloroacetyl)amino]-5-phenylthiophene-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 5-Methyl-2-thiopheneboronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,5-Dibromo-3-hexylthiophene is an organosulfur compound that reacts with aryl halides in the presence of copper to form arylthioethers in high yields. The reaction mechanism involves oxidative addition of the thiophene ring to give the corresponding radical anion. This radical anion then undergoes reductive elimination to generate the desired product and copper(II) sulfide. 2,5-Dibromo-3-hexylthiophene has been shown to inhibit growth of human MCF7 breast cancer cells and induce apoptosis by inhibiting protein synthesis. The optimal reaction conditions are at room temperature with a reaction time of 10 minutes.

Stability Unstable in Solution, Air Sensitive Applications 2-HYDROXYTHIOPHENOL (cas# 1121-24-0) is a useful research chemical.

5,5''-Dibromo-2,2':5',2''-terthiophene is a planar molecule with a tetrathiafulvalene core. The structure of the molecule consists of two fused rings: one containing two bromine atoms and the other containing five carbon atoms. The molecule is symmetrical across the central C=C bond.

3,4-Diamino-thieno[2,3-b]thiophene-2,5-dicarboxylic aciddiethylester is a chemical compound with the molecular formula C6H7N3O8S. It is the anhydride of 3,4 diaminothieno[2,3-b]thiophene 2,5 dicarboxylic acid and diethyl ethyl acetoacetate. This compound has been used in the synthesis of a number of other compounds. The salt form of this compound has been shown to be active against Mycobacterium tuberculosis and Mycobacterium avium complex.

Please enquire for more information about Methyl 3-(((4,4-dimethyl-2,6-dioxo-3,5-dioxanylidene)methyl)amino)thiophene-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Nitrothiophene-2-carboxaldehyde (5NT) is a chemical compound that belongs to the class of dihedral molecules. It is commonly used as an antimicrobial agent and has been shown to have amoebicidal activity in tissue culture. 5NT also inhibits cell growth and proliferation in certain bacteria, such as Staphylococcus aureus strains, by interfering with DNA replication and protein synthesis. Although 5NT is not active against other types of bacteria, it has been shown to be effective against MRSA in laboratory studies. The biological properties of 5NT are still being studied.

Please enquire for more information about Methyl 2-amino-5-phenylthiophene-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-[(Chloroacetyl)amino]-5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Bromo-2-thiophenecarboxylic acid is a reactive and toxic compound that can inhibit methionine aminopeptidase and glutamate dehydrogenase. It has been shown to be a good substrate for Suzuki coupling reactions, which are commonly used to synthesize pharmaceuticals. 5-Bromo-2-thiophenecarboxylic acid is also photophysical, meaning it absorbs light at specific wavelengths. It has been studied in molecular modeling and toxicity studies to determine its effects on cells.

Please enquire for more information about Methyl 2-[(chloroacetyl)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

5-Bromothiophene-3-carbaldehyde is a cyclic compound with an optical shift that can be used in transistors and as a semiconducting material. It is soluble in organic solvents, such as THF and DMF, and has been shown to have photophysical properties. 5-Bromothiophene-3-carbaldehyde is also a 1,3-dipolar cycloadduct that can undergo crystal x-ray diffraction. The heterocycles of this compound are phenyl groups. Thin films of this compound have been used for the study of its morphology.