Heterocycles with Sulphur (S)
Here you will find a class of organic compounds that contain a sulfur atom in the heterocyclic ring. Sulfur-containing heterocycles are crucial in the development of pharmaceuticals, agrochemicals, and materials due to their unique chemical properties and biological activities. These compounds are widely used in medicinal chemistry and materials science. At CymitQuimica, we provide a diverse selection of high-quality sulfur-containing heterocycles to support your research and industrial applications.
Subcategories of "Heterocycles with Sulphur (S) "
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Ethyl 2-Aminothiophene-3-carboxylate
CAS:Controlled ProductApplications Ethyl 2-Aminothiophene-3-carboxylate (cas# 31891-06-2) is a compound useful in organic synthesis.
Formula:C7H9NO2SColor and Shape:NeatMolecular weight:171.225-Bromo thiophene-2-aldehyde
CAS:5-Bromo thiophene-2-aldehyde is a trifluoroacetic acid derivative used as an activatable probe for the study of biomolecular interactions. This compound has been shown to be biocompatible and has a low cytotoxicity. 5-Bromo thiophene-2-aldehyde binds to malonic acid in the presence of x-ray radiation and forms a complex that can be detected by electrochemical impedance spectroscopy. The structure of this complex was determined by x-ray crystal structures. This probe is also able to bind to nitrogen atoms in proteins, which can be used to diagnose cancer resistance through protease activity. 5-Bromo thiophene-2-aldehyde is isolated as its hydrochloride salt, which can be purified with a suzuki coupling reaction.Formula:C5H3BrOSPurity:Min. 95%Color and Shape:Yellow PowderMolecular weight:191.05 g/mol2,6-Dimethylthiophenol
CAS:2,6-Dimethylthiophenol is a structural analog of the natural product sumatrana. It has been shown to be an effective catalyst for the cleavage of carbon-carbon bonds in organic molecules and fatty acids. 2,6-Dimethylthiophenol is unique because it contains two sulfur atoms that are part of a thiolate group, which can easily be oxidized to a sulfoxide or sulfone. This property makes 2,6-dimethylthiophenol an excellent reductant in reactions that require a metallacycle intermediate. The reactivity of this molecule is also influenced by its redox potential and the presence of nitrogen atoms. 2,6-Dimethylthiophenol was synthesized and studied using model compounds, yielding reaction yields as high as 98%.
Formula:C8H10SPurity:Min. 95 Area-%Color and Shape:Clear LiquidMolecular weight:138.23 g/mol2,5-Dibromothiophene
CAS:2,5-Dibromothiophene is a reactive intermediate that has been used in the synthesis of ondansetron hydrochloride. 2,5-Dibromothiophene can be prepared by the reaction of triethyl orthoformate and thiophene. The compound spontaneously undergoes bond cleavage to give the dibromo derivative followed by oxidation with aqueous hydrogen peroxide. 2,5-Dibromothiophene has been shown to have photocatalytic activity under visible light irradiation. This compound functions as a monomer in the polymerization of polythiophenes. 2,5-Dibromothiophene can also be used in palladium-catalyzed cross-coupling reactions with azasetron hydrochloride to form x-ray crystal structures and nmr spectra.Formula:C4H2Br2SPurity:Min. 95%Color and Shape:Colourless To Yellow LiquidMolecular weight:241.93 g/mol2-Bromothiophene
CAS:2-Bromothiophene is a brominated organic compound with six carbon atoms in a ring. It is synthesized by the Suzuki coupling reaction of 2-bromobenzene and aniline, which forms the pyrazole ring. The molecule can be used as a monomer for cationic polymerization to form polymers with high thermal stability. 2-Bromothiophene has been shown to be effective in treating chronic bronchitis, and can also be used as a photoelectron source.Formula:C4H3BrSPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:163.04 g/mol4,5-Dihydro-3(2H)-thiophenone-1,1-dioxide
CAS: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.Formula:C4H6O3SPurity:Min. 95%Color and Shape:Light (Or Pale) Yellow SolidMolecular weight:134.15 g/molMethyl 3-amino-5-methyl thiophene-2-carboxylate
CAS:Methyl 3-amino-5-methyl thiophene-2-carboxylate is a fine chemical that belongs to the group of useful scaffolds, versatile building blocks, useful intermediates for research chemicals and speciality chemicals. It can be used as reaction components in the synthesis of complex compounds. Methyl 3-amino-5-methyl thiophene-2-carboxylate is a high quality reagent with a wide range of applications in organic chemistry.Formula:C7H9NO2SPurity:Min. 95%Color and Shape:PowderMolecular weight:171.22 g/molThiophene-2-carboxamide
CAS:Thiophene-2-carboxamide is a synthetic chemical that is an inhibitor of the efflux pump, receptor activity, and recombinant cytochrome p450. It has been shown to be effective against colorectal carcinoma cells in vitro and in vivo. Thiophene-2-carboxamide also inhibits the mitochondrial membrane potential and hydrogen bond formation. This compound has potent inhibitory activity for the enzyme synthetase, which may be a potential drug target for cancer treatment. Nitrogen atoms are present in this molecule.
Formula:C5H5NOSPurity:Min. 95%Color and Shape:White PowderMolecular weight:127.17 g/molMethyl 4-methyl-3-[(N-propylalanyl)amino]thiophene-2-carboxylate HCl
CAS: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.Formula:C13H20N2O3S·HClPurity:Min. 95%Color and Shape:PowderMolecular weight:320.84 g/mol3-Bromothiophene-2-carbaldehyde
CAS: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.
Formula:C5H3BrOSPurity:Min. 95%Color and Shape:White To Yellow To Light Brown SolidMolecular weight:191.05 g/mol2-Acetylthiophene
CAS:2-Acetylthiophene is a chemical compound that contains thiophene and acetyl groups. It is a tetrazolium dye which can be used to study the Langmuir adsorption isotherm. 2-Acetylthiophene has been shown to have biological properties in vitro, including apoptotic effects in mammalian cells. 2-Acetylthiophene is an aryl halide with methyl ketones as its conjugate base. It can be synthesized by reacting 2-chlorothiophene with acetyl chloride in the presence of hydrochloric acid. The reaction can also be performed using phosphotungstic acid or hydrochloric acid as catalysts. 2-Acetylthiophene has been shown to have antifungal activity against Candida albicans and Saccharomyces cerevisiae, although it has no effect on Aspergillus niger.Formula:C6H6OSPurity:90%Color and Shape:Colorless Clear LiquidMolecular weight:126.18 g/mol3,3'-Dimethyl-2,2'-bithiophenyl
CAS:3,3'-Dimethyl-2,2'-bithiophenyl is a thermochromic polymeric compound that has been used as a colorant in polymers. The compound has a linear structure consisting of two thiophene rings with methyl groups at the 3 and 2 positions. The 3,3'-dimethyl group is attached to the second carbon atom of the thiophene ring and the 2,2'-bithiophenyl group is attached to the first carbon atom of the thiophene ring. The color changes from yellow to orange when heated to above 200 °C. This color change is due to conformational changes in the molecule that occur with thermal energy input.Formula:C10H10S2Purity:Min. 95%Color and Shape:Yellow PowderMolecular weight:194.32 g/molThiophene-3-carboxaldehyde
CAS:Thiophene-3-carboxaldehyde is an electron-rich, reactive chemical substance that can be used as a polymer film. It is a heterocyclic compound with a thiophene ring and a carbonyl group in the 3-position. Thiophene-3-carboxaldehyde is synthesized by reacting methyl ketones with glycol ethers. This reaction produces redox potential, malonic acid, and nmr spectra.Formula:C5H4OSPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:112.15 g/molMethyl 3-chlorosulfonylthiophene-2-carboxylate
CAS:Methyl 3-chlorosulfonylthiophene-2-carboxylate is a chemical compound that belongs to the family of thiophene carboxylic acid esters. It has been used for the synthesis of bioactive molecules, such as tenoxicam, and heteroarylations. Methyl 3-chlorosulfonylthiophene-2-carboxylate can be used in cross-coupling reactions with chloride as a reagent and is regiospecific. This chemical has also been shown to be reactive towards proteins, nucleic acids, and other biomolecules.
Formula:C6H5ClO4S2Purity:Min. 95%Color and Shape:PowderMolecular weight:240.69 g/mol3-Tetradecylthiophene
CAS:3-Tetradecylthiophene is a colorless liquid with a refractive index of 1.547, which has an onset of 10-20°C and a dilution of 0.01%. The compound has an absorption spectrum in the region of 230-390 nm, with a maximum at 340 nm and a quantum efficiency of 0.2%. 3-Tetradecylthiophene is used as a monomer for the preparation of polymer films and coatings. It can be copolymerized with other materials to produce polymers that are optically active due to their shift in position on the visible light spectrum.Formula:C18H32SPurity:Min. 95%Color and Shape:Clear Colourless Solid Or Liquid (May Vary)Molecular weight:280.51 g/molThiophene-2-sulfonamide
CAS: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).Formula:C4H5NO2S2Purity:Min. 95%Color and Shape:PowderMolecular weight:163.22 g/molMethyl thiophene-2-acetate
CAS:Methyl thiophene-2-acetate is a reaction product of methyl thiophene-2-carboxylate and nitric acid. It is a synthetic compound that has been used in the synthesis of primary alcohols, alkene and carboxylic acids. Methyl thiophene-2-acetate has been shown to be an effective reactant for the synthesis of hydrogenated polymers and solar cells. The resonance structures of this compound have been identified by nmr spectra. This compound can also form reaction products with nitrate, which can be used as a research tool for organic chemists.Purity:Min. 95%Methyl 3-amino-5-nitro-1-benzothiophene-2-carboxylate
CAS:Please enquire for more information about Methyl 3-amino-5-nitro-1-benzothiophene-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C10H8N2O4SPurity:Min. 95%Color and Shape:PowderMolecular weight:252.25 g/mol2-Chloro-N-[4-[(trifluoromethyl)thio]phenyl]propanamide
CAS:Please enquire for more information about 2-Chloro-N-[4-[(trifluoromethyl)thio]phenyl]propanamide including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C10H9ClF3NOSPurity:Min. 95%Color and Shape:PowderMolecular weight:283.7 g/molmethyl 3-(2-indol-3-yl-2-oxoacetylamino)thiophene-2-carboxylate
CAS:Please enquire for more information about methyl 3-(2-indol-3-yl-2-oxoacetylamino)thiophene-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this pagePurity:Min. 95%
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