Heterociclos con azufre (S)

2,4,6-Trimethylthiophenol (2,4,6-TMP) is an electron donor and a non-heme metal thiolate that is found in the active site of many enzymes. 2,4,6-TMP is a substrate for repair mechanisms that involve transfer reactions with other molecules. It can be used to create ternary complexes with nucleophilic attack or hydrocarbon solvents. X-ray crystal structures have been obtained showing that 2,4,6-TMP binds to amines and deuterium isotopes in the presence of light. 2,4,6-TMP has been shown to reduce azides to amines under conditions where hydrogen bonding does not occur.

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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.

Applications 4,5-dimethylthiophene-3-carboxylic acid (cas# 19156-52-6) is a useful research chemical.

2,3,5-Tribromothiophene is a solvent that is used in the synthesis of Pd catalysts. It can also be used as an additive for the growth of plants. 2,3,5-Tribromothiophene has been shown to be a good catalyst for cross coupling reactions and can be used for the synthesis of methyl ketones. This chemical has been shown to react with a Grignard reagent to produce bithienyl. 2,3,5-Tribromothiophene has many uses including being recycled and as a transition metal.

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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.

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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%.

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Please enquire for more information about 2-Amino-N-(3-methylphenyl)-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

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Tetrahydrothiophene-3-ol 1,1-dioxide is a metabolite of tetrahydrothiophene, which has been shown to have antiproliferative effects. Tetrahydrothiophene-3-ol 1,1-doxide inhibits the growth of human cervical cancer cells by inhibiting cell proliferation and inducing apoptosis in these cells. Tetrahydrothiophene-3-ol 1,1-dioxide binds to DNA and alters the expression of genes that are involved in the regulation of cell cycle progression and control. This compound also inhibits protein synthesis by binding to ribosomes and blocking protein synthesis. The compound can be detected in both plasma samples and plant tissue samples with chromatographic methods. Hydration or hydrogen chloride treatment can increase the solubility of this compound, making it easier to detect using analytical methods such as electrospray mass spectrometry.

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5-Formylthiophene-2-carbonitrile (5FT) is an agent that has been shown to be effective in treating altissima, hyalomma, and rusticana viruses. It has also been shown to have clinical efficacy against hepatitis B virus infections and acute phase sanguineus virus infections. 5FT inhibits the viral nucleotide polymerase and is able to kill viruses such as rhipicephalus sanguineus and listeria monocytogenes. 5FT has also been shown to inhibit the replication of human herpesviruses, including varicella zoster virus and cytomegalovirus. This compound may exert its antiviral effects by inhibiting the synthesis of viral proteins involved in transcription, replication, or assembly.

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Applications 4,5,6,7-Tetrahydro-7-oxo-benzo[b]thiophene-4-carbonitrile is a useful synthetic intermediate.

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