Heterocycles with Sulphur (S)

Please enquire for more information about 2-Amino-N-(2-methoxyphenyl)-5,6-dihydro-4H-cyclopenta[b]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 ethyl 2-[(2-chloroacetyl)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 5-Ethylthiophene-2-carbonyl chloride 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-isothiocyanato-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 4-Bromo-5-ethylthiophene-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 N-Phenyl-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

Please enquire for more information about 2-Amino-6-tert-amyl-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

5-Amino-2-thiophenecarboxylic acid methyl ester (ATM) is an antibacterial drug which inhibits the growth of bacteria by binding to the p2y1 receptor on the bacterial cell membrane. ATM inhibits platelet aggregation, and is used for the treatment of thrombotic disorders such as myocardial infarction and stroke. This compound has also been shown to interact with chloride ions, ammonium ions, and bacteriostatic agents such as tetracycline. ATM interacts with hydrophobic regions in proteins, leading to a decrease in their activity.

Please enquire for more information about 2-Amino-N-cyclopentyl-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-Ethynylthiophene is a solvent that can be used to synthesize organic compounds. It has tautomeric forms and reacts with many functional groups, including alcohols, amines, and carboxylic acids. The synthesis of 2-ethynylthiophene involves the hydrothiolation of terminal alkynes in the presence of dicarbonyl compounds. This reaction system produces a solvated product that can be crystallized as its hydrocarbon form. 2-Ethynylthiophene can also be used as a ligand for supramolecular chemistry and electron spin resonance (ESR) spectroscopy.

Please enquire for more information about Isopropyl 2-amino-4-(4-cyclohexylphenyl)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-(4-ethylphenyl)-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 3-Methylthiophenylboronic acid, pinacol ester 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-sec-butylphenyl)-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 4-Methoxy-2-(4-methoxyphenyl)-benzo[b]thiophene 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-Phenylthiophene-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 6-amino-5-thioxo-4,6-dihydro-4,6-diazabenzo[b]thiophen-7-one 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-cyclopentyl-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 4-Methylthiophene-2-sulfonyl chloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,5-Dichloro-3-methylthiophene is an acyclic, aromatic heterocycle that has a five-membered ring. It is hydrophobic and can be used as a solvent for organic reactions. The chloride atom on the central carbon in this compound is electron withdrawing and it is believed to have a stabilizing effect on the molecule. When 2,5-dichloro-3-methylthiophene reacts with another molecule of 2,5-dichloro-3-methylthiophene or with a molecule containing an electronegative atom (e.g., oxygen), it undergoes dehydration to form 1,4,2,6 tetrahydropyridine. This reaction produces two molecules of water as byproducts. 2,5 dichloro 3 methyl thiophene hydrolyzes easily in acidic conditions to produce hydrogen chloride gas and 1 4 2 6 tetrahydropyridine hydrochlor

Please enquire for more information about 2-Amino-4-trifluoromethyl-thiophenol, HCl 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-3-fluorobenzoyl-5-methylthiophene 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-2-boronic acid, neopentyl glycol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications (E)-1-(Benzo[b]​thiophen-​2-​yl)ethanone Oxime is an isomer of N-​(1-​Benzo[b]​thiophen-​2-​yl-​ethyl)​-​hydroxylamine a reagent used in the preparation of Zileuton, an anti-asthmatic drug. References Guinchard, X. et al.: J. Org. Chem., 73, 2028 (2008)

Please enquire for more information about Isopropyl 2-amino-5-{[(2,4-dimethylphenyl)amino]carbonyl}-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 2-(5-Methylthiophen-2-yl)aniline hydrochloride 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]thiophene-2-carboxylic acid hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-(2-Ethylhexyl)thiophene is a molecule with two thiophene rings that are connected by an ethylene bridge. The molecule has an optical band gap of 1.5 eV, which is higher than the 1.4 eV band gap of the unsubstituted thiophene ring. This intermolecular interaction leads to increased absorption in the visible region of the spectrum and increased efficiencies in solar cells. 3-(2-Ethylhexyl)thiophene can be used as a building block for a variety of materials, including solar cells, organic light emitting diodes (OLEDs), and field-effect transistors (FETs). It can also be used as a precursor for other molecules through methylation reactions.

Please enquire for more information about 9-(3-Deoxy-3-fluoro-beta-D-ribofuranosyl)-2-chloro-6-(thiophen-3-yl)purine 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 5-bromo-3-(2,2,2-trichloroacetamido)thiophene-2-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 9,10-Dihydro-4H-benzo[4,5]cyclohepta[1,2-b]thiophen-4-one 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-Ethyltetrahydrothiophen-3-amine 1,1-dioxide hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Phenylthiophene is a polymer film that is composed of monomers with dipole moments. 3-Phenylthiophene has been shown to have an inverse sol-gel transition in the presence of sodium sulfide and water. The morphology and optical properties of 3-phenylthiophene films are dependent on the concentration of monomer and temperature. It has a polarizability of 0.65 D, which can be analyzed using nmr spectra at room temperature. 3-Phenylthiophene has been used as an analytical method for β-unsaturated ketones, electrochemical impedance spectroscopy, and vibrational analysis.

6-Bromo-3-chloro-1-benzothiophene-2-carboxylic acid is a bifunctional reagent that can undergo cycloaddition or cyclization reactions with alkenes and alkynes. It is used in the synthesis of lactones and substituted benzoic acids. The reaction mechanism of 6-bromo-3-chloro-1-benzothiophene-2 carboxylic acid involves an elimination, followed by a Grignard addition to the carbonyl group. This product is also used in the synthesis of esters, anhydrides, and amides. It is hydrolyzed by water to release 6 bromo 3 chloro 1 benzothiophene 2 carboxylic acid.

5,6-Dihydro-4H-cyclopenta[b]thiophene-2-carboxylic acid is a potent antibacterial agent that has been shown to be effective against methicillin-resistant Staphylococcus aureus and other bacteria. This compound is active against the Gram positive bacteria S. aureus, S. pyogenes, S. pneumoniae, and S. erythraea as well as the Gram negative bacteria P. aeruginosa, E. coli, C. jejuni, and K. pneumoniae at low concentrations (0.1-1 µM). It also has antifungal activity against C. albicans at high concentrations (10-20 µM). The molecular mechanism of action for 5,6-dihydro-4H-cyclopenta[b]thiophene-2-carboxylic acid is not known but it may involve resonance

Please enquire for more information about 5-(1H-Pyrazol-1-ylmethyl)thiophene-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications A hydroxy derivative of dibenzothiophene. Coal model compound used in chemical coal cleaning studies with molten hydroxides. References Nowak, M.A. et al.: Coal Prep., 7, 29 (1989); Nishioka, M. et al.: Anal. Chem., 57, 1327 (1985);

Please enquire for more information about Propyl 2-amino-4-(4-fluorophenyl)-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 Methyl 5-chloro-3-(morpholin-4-ylsulfonyl)thiophene-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Methyl 4-methyl-3-[(N-propylalanyl)amino]thiophene-2-carboxylate HCl is a local anesthetic. It has been shown to be effective in the treatment of dental pain. Methyl 4-methyl-3-[(N-propylalanyl)amino]thiophene-2-carboxylate HCl acts by inhibiting the sodium channels in nerve cells, thereby blocking the transmission of pain signals and causing muscle relaxation. This drug also provides relief from anxiety, tension, and fear. Methyl 4-methyl-3-[(N-propylalanyl)amino]thiophene-2-carboxylate HCl has a rapid onset of action, with effects lasting up to 45 minutes. The drug is metabolized by hydrolysis to methyl 3-(aminocarbonyl)thiophene carboxylate and excreted in urine as metabolites.

Please enquire for more information about 2-Amino-N-(2-furylmethyl)-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

4,5-Dihydro-3(2H)-thiophenone-1,1-dioxide is a pyridine derivative with a functional group that is used as an antiviral agent. It blocks the serine protease by binding to the active site of the enzyme and preventing it from functioning. 4,5-Dihydro-3(2H)-thiophenone-1,1-dioxide has a carbonyl group that can be used for catalysis and hydroxy groups that are important for hydrogen bonding. This compound also has quinoline derivatives that act as cyclic structures.

Please enquire for more information about 2-Amino-4-ethyl-N-(2-methoxyphenyl)-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 4-Aminotetrahydrothiophene-3-ol 1,1-dioxide 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-n-Octyl-2,2'-bithiophene 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 4-methylthiophene-2-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 4-n-Octyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene 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-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Chlorothiophene is a fluoroquinolone antibiotic that inhibits the DNA gyrase and topoisomerase IV, which are enzymes that maintain the integrity of bacterial DNA. It binds to bacterial 16S ribosomal RNA and inhibits protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division. 3-Chlorothiophene has been shown to be effective against P. aeruginosa, although is not active against acid-fast bacteria such as Mycobacterium tuberculosis or Mycobacterium avium complex. 3-Chlorothiophene has been shown to have carcinogenic potential and should be handled with care because it can cause irritation on contact with skin or eyes. 3-Chlorothiophene may also have photoelectron effects on metal surfaces, which could cause corrosion if used in large quantities in water treatment systems.

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

Intermediate in the synthesis of canagliflozin

Please enquire for more information about 2-Amino-N-(2,5-dichlorophenyl)-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

2-Cyano-5-bromothiophene is a compound with an optical yield of 0.064 at 557 nm. It has been shown to be unreactive and stable in the presence of oxygen, nitrogen, and water. The bromine atom in 2-cyano-5-bromothiophene is capable of undergoing a palladium-catalyzed coupling reaction with electron deficient olefins to form aryl bromides. These reactions are efficient and selective, giving yields up to 95% after 24 hours. 2-Cyano-5-bromothiophene also has antibacterial activity against Gram positive bacteria, including methicillin resistant Staphylococcus aureus (MRSA). This property may be due to its ability to cleave DNA by generating reactive oxygen species (ROS) when irradiated with light. 2-Cyano-5-bromothiophene is fluorescent and can emit

3-DodeCyl-2-ethynylthiophene is a polyunsaturated ketone that is used as a ligand in coordination chemistry. It is a colorless, crystalline solid with a molecular weight of 204.3 g/mol. 3-DodeCyl-2-ethynylthiophene has been shown to be able to form x-ray active complexes with metal ions such as copper(II) and zinc(II). The mechanism of the complex formation is believed to involve an electrophilic substitution reaction between the thiol group in 3-dodecylthiophene and the metal ion. This reaction leads to an intermediate complex that can be stabilized by intramolecular hydrogen bonding.

Please enquire for more information about 2-Amino-4-ethyl-5-methylthiophene-3-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Propyl 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 N-(1-Oxo-1,3-dihydro-2-benzofuran-5-yl)thiophene-2-sulfonamide 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-aminothiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page