Heterocycles with Sulphur (S)

Please enquire for more information about Ethyl 2-amino-4-(4-ethoxyphenyl)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 3-Nonyl-5-thiopheneboronic 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 2-Amino-6-methyl-N-(2-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 2-Amino-6-tert-amyl-N-(2-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-Methylbenzo[b]thiophene is an inorganic chemical that has been found to be toxic to cells. The cytotoxicity of 5-methylbenzo[b]thiophene is strain-dependent and was observed in wild-type cells, but not in a strain with a mutation in the sulfite reductase gene. This chemical also affects the concentration of Ca2+ ions and carbon sources, which are important for cellular metabolism. The linear regression analysis suggests that ionizable groups may be responsible for this toxicity. Acute toxicities were seen at high concentrations and include oxidative stress, cell death, and DNA damage.

5-(2-Chlorophenyl)thiophene-2-carboxylic acid is a reagent, complex compound, and useful intermediate that belongs to the class of fine chemicals. CAS No. 500604-91-1 is a speciality chemical that is used as a versatile building block in research chemicals and as a reaction component for the synthesis of new drugs. It is also an excellent building block for synthesizing 1,4-benzothiazepines and other heterocyclic compounds.

Please enquire for more information about 4-Fluoro-2-methylthiophenol 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-5-methyl-4-phenyl-3-thiophenecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-(Trimethylsilylethynyl)thiophene is a reactive chemical that is used in the synthesis of other chemicals. It has a carbonyl group and three functional groups, which are the alcohol, ketone, and chloride. This compound can be synthesized by reacting aldehydes with trifluoromethyl chloroformate and then adding trimethylsilylacetylene. 3-(Trimethylsilylethynyl)thiophene reacts with alcohols to form ketones and with chloroformates to form chlorothiophenes. It also reacts with fluoride ions to produce fluoro compounds.

Please enquire for more information about Methyl 2-amino-4-cyclopropylthiophene-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 Tetrahydrothiophene-3,4-diamine 1,1-dioxide dihydrochloride 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-(Pyrrolidin-1-ylsulfonyl)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 1-Chloronaphtho[2,1-b]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 4-Ethyl 2-methyl 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

Please enquire for more information about 2-Amino-N-(2-chloro-5-nitrophenyl)-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-Chlorotetrahydrothiophene-3-ol 1,1-dioxide is a nucleophilic reagent that is used in organic synthesis. It reacts with electron-deficient alkylating agents to form mixed alkyl chlorides. 4-Chlorotetrahydrothiophene-3-ol 1,1-dioxide has an optimum reaction temperature of -78 degrees Celsius and can react with a wide range of electron rich and electron deficient groups. This compound is a white solid at room temperature.

Please enquire for more information about 2-Amino-6-methyl-N-(4-methylbenzyl)-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 2-Bromo-3-butylthiophene 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-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 4-Methylthiophene-2-boronic 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 2-Amino-N-(4-methylbenzyl)-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

Ethyl 2-methylthiophene-3-carboxylate is an intermediate in the synthesis of a variety of organic compounds, including fluoroalcohols and pharmaceuticals. The synthesis is based on the Wittig reaction, which involves the formation of a wittig reagent from a magnesium halide and a carboxylic acid chloride. This reagent reacts with an aromatic compound such as thiophene to form an alkyl group at the α position. The alkylation proceeds intramolecularly to form ethyl 2-methylthiophene-3-carboxylate without any need for an external base. Ethyl 2-methylthiophene-3-carboxylate can be obtained through a scalable, efficient method that uses Grignard reagents as starting materials.

Please enquire for more information about methyl 3-(((4,4-dimethyl-2,6-dioxocyclohexylidene)methyl)amino)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 Methyl 2-amino-4-(4-isobutylphenyl)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-tert-Butyl 4-ethyl 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

Please enquire for more information about 2-Amino-4-(4-methylphenyl)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]-4,5-dimethyl-3-thiophenecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,5-Dithiophen-2-yl-thieno[3,2-b]thiophene (DTTS) is an organic semiconductor that has potential applications in polymer solar cells. The polymerization of DTTS can be achieved through a number of methods including thermal evaporation or solution-based processing. This polymerization produces a low molecular weight material with an interchain distance of approximately 2.5 Å and a redox potential approximately 0.5 V more positive than that of the parent compound. The photovoltaic properties of DTTS have been studied by systematically varying the methyl ester substituent at the para position and determining the effect on the carrier transport, kinetic stability, and optical absorption spectra. These studies show that when this substituent is methylated, DTTS has increased photovoltaic efficiency due to a reduced electron transport rate between chains and improved charge transfer kinetics.

2-Methoxythiophene is a molecule that belongs to the class of aromatic heterocycles. It is an intermediate in the synthesis of other molecules, such as carbonyl compounds, which are important for cancer diagnosis. 2-Methoxythiophene has been used to produce acetylated derivatives and then analyzed by solid phase microextraction followed by gas chromatography and mass spectrometry. The chloride ion can be detected by gas chromatography with flame ionization detection. 2-Methoxythiophene can also be used to detect cancer cells in urine samples because it reacts with nucleophilic groups on the cancer cells and cleaves bonds between chloride ions and nucleophilic groups on the cell surface. This reaction produces hydrogen chloride, which is detectable by gas chromatography.

Please enquire for more information about 5-Bromo-1-benzothiophene-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

4,4,4-Trifluoro-1-(Benzo-[b]-thiophen-3-yl)butane-1,3-dione is a compound that is extracted from copper. The complex has been shown to be reproducible in chloroform and perchloric acid. It has also been shown to be sensitive to hafnium and zirconium. The solvents used in the extraction process are ethanol and perchloric acid.

3-Formyl-4-thiopheneboronic acid is an organic compound that is used in the functional theory of polycyclic compounds. It has intramolecular, intermolecular and spectroscopic properties. The functional theory of 3-Formyl-4-thiopheneboronic acid is based on the wavelength shift of a chromophore (e.g., fluorescence). This compound can be used in biomolecules as a fluorescent molecule and yields an acceptor energy transfer from the donor to the acceptor. 3-Formyl-4-thiopheneboronic acid has been shown to have a solid state structure with fluorescence properties.

Please enquire for more information about (4S)-4-Methyl-2-oxo-[1,3,2]dioxathiolane-4-carboxylic acid methyl 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 [2-(DiMethyl-thiophen-2-yl-silanyl)-phenyl]-Methanol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Thiophene-2-sulfonamide is a fungal biomass inhibitor that binds to specific receptors in the human liver, which decreases the production of hemolytic substances. Thiophene-2-sulfonamide has been shown to have a reversible effect on the metabolism of peptide hormones and metabolic disorders in vivo. The drug also has diagnostic properties and can be used to measure receptor binding activity. Thiophene-2-sulfonamide is an intermediate in the synthesis of diagnostic agents such as 3-(4'-aminophenyl)thiophene-2,5-diol (APTD).

Please enquire for more information about Methyl 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 Methyl 3-[(3-chloropropanoyl)amino]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 6-Methyl-1-benzothiophene-3-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 2-Chloro-3-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 Isopropyl 2-[(chloroacetyl)amino]-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

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Please enquire for more information about Ethyl 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

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

3-Nonylthiophene is a colorless liquid that is used as a solvent for printed circuit boards and has been shown to be useful in the manufacture of optical devices. 3-Nonylthiophene can be extracted from the surface of an object using solid phase microextraction, which involves the use of a porous material (e.g., cellulose) that contains a sorbent material (e.g., silica) at one end and an extraction solution (e.g., methanol) at the other end. The sorbent material absorbs 3-nonylthiophene from the object surface, which is then eluted with a solvent, such as methanol or water, to produce an extract containing 3-nonylthiophene. This extract can then be analyzed by various techniques, including diode array detection and liquid chromatography. 3-Nonylthiophene can also be analyzed using photooxidation with di

Please enquire for more information about Methyl 3-(pyrrolidin-1-ylsulfonyl)thiophene-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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2,5-Dichlorothiophene is an efficient synthetic method for the preparation of sodium sulfide. It has been used as a building block for other syntheses, such as the synthesis of chalcones. The antimicrobial activity of 2,5-dichlorothiophene is due to its chlorine atom and alkoxy radical. The chlorine atom can react with thiols in bacterial cells and the alkoxy radical can react with proteins. This reaction leads to cell death or inhibition of protein synthesis, which prevents the bacteria from reproducing. 2,5-Dichlorothiophene has also been shown to have cancer resistance properties due to its ability to inhibit protease activity.

Please enquire for more information about 4-Formyl-2-methoxyphenyl 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 Methyl 2-isothiocyanato-4,5,6,7,8,9-hexahydrocycloocta[b]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 Methyl 5-benzyl-2-isothiocyanatothiophene-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 2-amino-4-(4-ethylphenyl)-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 p-Thiophenyl phenyl diphenyl sulfonium hexafluoroantimonate 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)-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 2-Amino-6-tert-amyl-N-(3-methoxyphenyl)-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

3-Iodothiophene is a functional group that contains an electron-withdrawing terminal alkyne. This compound reacts with copper to form the corresponding copper(I) 3-iodothiophene complex, which has been shown to react with malonic acid to form methyl ketones. The interaction constant between 3-iodothiophene and copper is 2.0 x 10^6 M^(-1). 3-Iodothiophene reacts with a variety of other compounds including magnesium, c1-4 alkyl, and Grignard reagents. Palladium-catalyzed coupling reactions have been performed using this compound as a starting material.

Please enquire for more information about (5-(HydroxyMethyl)thiophen-3-yl)boronic 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-4-(2-furyl)thiophene-3-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Bromobenzo[b]thiophene is an organic molecule that acts as a thrombin inhibitor. It binds to the active site of thrombin, which prevents the conversion of prothrombin to thrombin. 5-Bromobenzo[b]thiophene is also used in photochemistry and fluorescence spectroscopy. In addition, it has been shown to be able to cross-couple with various functional groups, such as chlorides, phosphines, and halides. The mechanistic properties of 5-Bromobenzo[b]thiophene have been studied extensively using a variety of techniques. Furthermore, this molecule can be synthesized in many different isomers, which can have different reactivity profiles and properties.

3-Aminothiophene-2-carboxamide is an antimicrobial agent that belongs to the class of quinazolinones. It is a phosphotungstic acid derivative with antibacterial activity. 3-Aminothiophene-2-carboxamide inhibits bacterial growth by binding to bacterial enzyme and inhibiting its function. 3-Aminothiophene-2-carboxamide has been shown to inhibit the growth of bacteria in vitro, including methicillin resistant Staphylococcus aureus and Enterobacter cloacae, but not Pseudomonas aeruginosa or Escherichia coli. 3-Aminothiophene-2-carboxamide has been shown to be effective against gram positive bacteria such as Staphylococcus aureus and Enterococcus faecalis, but not against gram negative bacteria such as Pseudomonas aeruginosa or Escherichia coli. The compound

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

3-Oxo-2,3-dihydrobenzo[b]thiophene1,1-dioxide is an antifungal drug that has been shown to have a broad spectrum of activity against both bacteria and fungi. It inhibits the synthesis of cell wall components by binding to the enzyme enoyl reductase in the cytoplasmic membrane of fungi. This binding prevents the reduction of 3-oxohexanoyl coenzyme A and blocks fatty acid synthesis. The methylene group on this molecule is able to act as an electron acceptor, which increases its polarizability and therefore its dipole moment. This increased dipole moment enhances the antibacterial activity of 3-Oxo-2,3-dihydrobenzo[b]thiophene1,1-dioxide.