Heterociclos con azufre (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

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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.

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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.

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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