Heterocycles with Sulphur (S)

2-Methylthiophenothiazine is a phenothiazine that is used as an antibiotic. It has been shown to be effective against drug-resistant tuberculosis and other bacteria. 2-Methylthiophenothiazine inhibits the growth of bacteria by binding to DNA and RNA, which prevents protein synthesis and replication. The operational mechanism of this drug is not well understood, but it has been shown to be an effective treatment for tuberculosis. This drug also acts as an efflux pump inhibitor, which may contribute to its effectiveness. 2-Methylthiophenothiazine has also been shown to have efficiencies in acceptor cells such as Mycobacterium smegmatis, Escherichia coli, and Pseudomonas aeruginosa.

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

Dithieno[3,2-b;2',3'-d]thiophene-2,6-dicarbaldehyde is a transition metal complex that has been shown to be luminescent and thermally stable in organic electroluminescent devices. It has also been found to have high electron transport properties. The efficiency of the device is proportional to the transition temperature of the molecule and its wavelength. This molecule is a good candidate for molecular organic light emitting diodes due to its high thermal stability and efficiency.

Methyl 1-benzothiophene-2-carboxylate is an organic compound that can be prepared by electrolysis of a solution of dimethylformamide in the presence of a platinum electrode. It is used as a precursor to other chemical compounds, such as dibenzothiophene and benzothiazolium salts. The compound is also used in cyclic voltammetry and cyclic voltammetric methods. Methyl 1-benzothiophene-2-carboxylate is a dimer with two identical anionic radicals attached to each benzene ring. The electron affinity for these radicals is very high due to resonance stabilization which leads to efficient electron transfer from the electrode to the radical anion.

Please enquire for more information about N-Allyl-5-bromothiophene-2-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Dibenzothiophene 5,5-dioxide is a sulfone that is used as a surfactant in detergent compositions. It has the ability to form strong hydrogen bonding interactions with other molecules. Dibenzothiophene 5,5-dioxide can be activated by magnesium salt and biphenyl, which can lead to light emission. This compound also has redox potentials and transport properties. Dibenzothiophene 5,5-dioxide is used in polymerase chain reactions and has been shown to have picolinic acid activity.

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Applications Methyl 5-Chloro-3-(Chlorosulfonyl)Thiophene-2-Carboxylate (cas# 126910-68-7) is a useful research chemical.

Applications Used in the preparation of sulfur aroma compounds.

Please enquire for more information about N-Butyloxycarbonyl-3-[4-(imidazol-1-ylmethyl)phenyl]-4,5-diisobutylthiophene-2-sulfonamide 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 2-Amino-6-tert-butyl-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 4-Bromo-2-thiophenecarbonyl chloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Amino-tetrahydro-thiophene-3-carboxylic acid is a heterocyclic compound that belongs to the thiophene class of compounds. It has the chemical formula (CH3)2C=CS(CH2)2NH2. 3-Amino-tetrahydro-thiophene-3-carboxylic acid is an amino acid derivative and can be used as a building block in organic synthesis. It can also be used in the production of other compounds, such as aralkyl derivatives. The crystal structure was determined by XRD and crystallographic analysis.

Please enquire for more information about Ethyl 5-(trifluoroacetyl)-2-thiophenecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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3-(2-Bromo-acetyl)-5-chloro-thiophene-2-sulfonic acidamide is a research chemical that inhibits the enzyme carbonic anhydrase. This drug is a thioether with a bromohydrin and hydroxylamine functional group. It can be used as a reagent for hplc analysis, which is useful for identifying unknown compounds in samples. 3-(2-Bromo-acetyl)-5-chloro-thiophene-2-sulfonic acidamide has an ionizable group, which makes it useful for titration experiments.

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Please enquire for more information about 3-(3-Chloro-4-methoxybenzoyl)-4H,5H,6H-cyclopenta[B]thiophen-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Methyl 5-chloro-4-nitro-2-thiophenecarboxylate is an organic compound that is used as a ligand in asymmetric catalysis. It reacts with iridium and furan to form allylated compounds. It is also used in the synthesis of cyclic compounds with chiral centers because it can be easily converted into the corresponding enantiomer. Methyl 5-chloro-4-nitro-2-thiophenecarboxylate can be synthesized from dicarbonate and nitrobenzene, which are both easily available commercially.

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2-Iodo-3-hexylthiophene is a monomer that can be used in the synthesis of heterojunction photovoltaic devices. This compound, which has an asymmetric carbon atom, exists as two isomers: 2-iodo-3-hexylthiophene and 3-iodo-2-hexylthiophene. The former is more stable and has an electron affinity that is higher than that of the latter. When magnesium is added to these compounds, they react with each other to form a complex. The acceptor molecule then reacts with the complex and catalysis occurs, forming a functional theory. This process is called solid phase synthesis. Gel permeation chromatography can be used to separate the different compounds from each other. FTIR spectroscopy can be used to analyse the structure of 2-iodo-3-hexylthiophene and determine its purity.br>br>

Please enquire for more information about 2-(4-Methoxyphenyl)benzothiophene-6-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Ethylthiophene-2-boronic acid (ETBA) is a boronic acid that can reversibly bind to a wide range of organic compounds. It has been shown to have antioxidant properties and is being investigated as an additive for detergents, marine bacterium screening, and research. ETBA has been shown to inhibit the growth of bacteria by binding to the active site of enzymes such as 5-lipoxygenase in marine bacterium. This mechanism may be due to its ability to scavenge free radicals or chelate metal ions.

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3,5-Diisobutyl-1,2,4-trithiolane is a volatile organic compound that is liquid at room temperature. It has been identified as an α-tocopherol degradation product. The identification of 3,5-Diisobutyl-1,2,4-trithiolane was performed by GC/MS analysis of extracts from oxidized lipids and volatiles from thermally oxidized alkylpyrazines. This compound is formed during the oxidation of α-tocopherols under acidic conditions with thermal treatment. There are two mechanisms for the formation of 3,5-Diisobutyl-1,2,4-trithiolane: it can be generated by the reaction between aldehyde and cysteine or it can be generated by the reaction between α-tocopherol and lipid peroxidation products.

Please enquire for more information about N-Butyloxycarbonyl-3-[4-(imidazol-1-ylmethyl)phenyl]-4-benzyl-5-isobutylthiophene-2-sulfonamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,5-Dichlorothiophene-3-carboxylic acid is a triazine. It is a supramolecular anion that has been found to interact with cations and carboxylates. The interaction of 2,5-Dichlorothiophene-3-carboxylic acid with pyrimethamine has been studied using cocrystal X-ray diffraction studies. These studies have shown that the carboxylate group of 2,5-Dichlorothiophene-3-carboxylic acid interacts with the pyrimethamine molecule through hydrogen bonds. This interaction may be due to the close proximity of these two molecules in the crystal lattice.

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3-Propylthiophene is a molecule that consists of three carbon atoms and six hydrogen atoms. The molecule has been shown to have interactions with other molecules, such as asymmetric synthesis or desulfurization. 3-Propylthiophene is used in the activation energy process and can be found in the gaseous state. It has been shown to have a linear growth pattern when heated at high temperatures, which can be an enthalpic process. 3-Propylthiophene has been shown to have an activation energy of 30 kJ/mol and is found in analytical methods for sulfide and sulfoxide compounds.

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3-Bromo-2-chlorothiophene is a chemical that belongs to the group of probe molecules. It has been used as an electrochemical probe for mechanistic studies in chemistry and biology. 3-Bromo-2-chlorothiophene may be used to generate potentials or yields, which can be determined by cyclic voltammetric measurements. 3-Bromo-2-chlorothiophene has been shown to have low toxicity in animal studies, but it is a strong carbanion forming agent for magnesium.

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Methyl 3-isocyanatothiophene-2-carboxylate is a potential agent that can be used to treat prostate cancer. It is an antagonist of the prostatic α1A adrenergic receptor and has been shown to inhibit the synthesis of PGE2, which is a prostaglandin that has been implicated in prostate cancer tumorigenesis. Methyl 3-isocyanatothiophene-2-carboxylate binds to the α1A subtype of the adrenergic receptor with high affinity, showing selectivity for this receptor subtype. The compound was synthesized from methyl thiobenzoate and potassium cyanide and has been shown to have selective binding properties in functional assays and binding assays.

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3-Chlorobenzo[b]thiophen-2-carbonyl chloride (3CBTC) is a triazine derivative that is synthesized to be used as an antibiotic. 3CBTC inhibits the growth of bacteria by binding to the ribosomes and preventing protein synthesis. It also has significant interactions with amines, aldehydes, oxazolones, piperidine, pyrazoles, aminopyridine and thionyl chloride. 3CBTC has been shown to inhibit the growth of Gram-positive and Gram-negative bacteria such as Streptococcus pneumoniae, Staphylococcus aureus, Enterococcus faecalis and Pseudomonas aeruginosa.

2-Ethylthiophenol is a hydrogenated organosulfur compound that is used as a reagent in synthetic chemistry for the conversion of hydrocarbons to more valuable products. It can also be used to desulfurize olefins and carbonyl compounds. 2-Ethylthiophenol reacts with ruthenium complexes to give thermally stable, functionalized molecules. 2-Ethylthiophenol has been shown to cleave bonds in organic molecules with the aid of active oxygen, such as hydroxyl radicals and peroxides. The reaction mechanism for this process is not yet known due to the lack of x-ray structures of 2-ethylthiophenol.

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Methyl 2-amino-6-tert-butyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate (MTB) is a lead compound that activates the retinoid X receptor. It is a potent activator of peroxisome proliferator activated receptor α (PPARα), and has been shown to protect against Alzheimer's disease in mice by reducing β amyloid levels. MTB also has neuroprotective effects and may be useful in the treatment of other neurodegenerative diseases such as Parkinson's disease.

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