Heterocycles with Sulphur (S)

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

Please enquire for more information about 2,6-Dibromo-4,4-dihexyl-4H-silolo[3,2-b:4,5-b']dithiophene including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Nitrothiophene-4-carboxylic acid is a nitro compound that is used as a chemotherapeutic agent. It has been shown to have affinity for DNA and inhibits the synthesis of nucleic acids, which leads to cell death. This drug is also mutagenic in kinetic assays. The acetylation of 2-nitrothiophene-4-carboxylic acid yields an N-acetyl derivative, which can be hydrolyzed by hydroxylamine to yield a methyl ester. Nitrothiophene-4-carboxylic acid has been shown to be mediated by nitro groups, with substituent effects on the enzyme activity and thermodynamic parameters.

2-Amino-5-methylthiophene-3-carboxylic acid is a medicinal compound that has been shown to have effects on the central nervous system, including the neurotransmission of serotonin. The receptors for 2-amino-5-methylthiophene-3-carboxylic acid are G protein coupled. Inhibition of this receptor leads to a reduction in neurotransmission and an improvement in mental disorders. This drug also has an acidic nature, which allows it to react with oxidizing agents and degradative enzymes. It has been shown that 2-amino-5-methylthiophene 3 carboxylic acid is stereospecific, meaning that it will only bind to one form of the receptor molecule. The onset of 2 amino 5 methylthiophene 3 carboxylic acid is rapid and its activity is constant over time. 2 aminothiazole 5 methyl carboxylate is a medicinal compound that has

Please enquire for more information about 5-(Aminocarbonyl)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 5-Amino-N-methyl-1-benzothiophene-2-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 Propyl 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 1,3-Dimethyl-5-[5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-thiophen-2-ylmethylene]-pyrimidine-2,4,6-trione including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 5-(Trifluoromethyl)benzo[b]thiophene-2-carboxylic acid methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page

Methyl-2-formyl-4-thiophenecarboxylate is a high quality reagent that is useful as an intermediate in the synthesis of complex compounds. It has a CAS number of 67808-66-6 and can be used as a building block in the synthesis of biologically active molecules. Methyl-2-formyl-4-thiophenecarboxylate is also a versatile building block that can be used to synthesize speciality chemicals, such as research chemicals and reaction components. This chemical has been shown to have many uses in organic synthesis, including being used for the preparation of pharmaceuticals. Methyl 2 formyl 4 thiophenecarboxylate is also useful for the production of fine chemicals, such as dyes and fragrances.

Please enquire for more information about 5-(4-Nitrophenyl)thiophene-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Thiopheneacrylic acid (2-TAA) is a potential use in the treatment of herpes simplex virus. It has been shown to inhibit viral replication by absorbing UV radiation, which alters the nucleotide sequence of the virus's DNA. 2-TAA is also soluble in water and an effective electron donor, which may enhance its antiviral activity. The enantiomeric form of 2-TAA has shown greater potency against herpes simplex virus than the mesomorphic form. 2-TAA was synthesized from malonic acid and hydrogen chloride gas in a reaction with an excess of thiopheneacrylic acid, which produced 2-thiopheneacrylic acid as a kinetic product. This reaction was found to produce a blood sample with a negative result for HIV 1 and HIV 2 antibodies.

Please enquire for more information about Propyl 2-amino-5,6,7,8-tetrahydro-4H-cyclohepta[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 ethyl 2-amino-4-(4-chlorophenyl)-3-thiophenecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 5-Pyridin-2-ylthiophene-2-carbaldehyde 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-ethylthiophene-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 Methyl 2-amino-7-methoxy-4,5-dihydronaphtho[2,1-b]thiophene-1-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-Amino-N-(2-ethoxyphenyl)-4,5,6,7,8,9-hexahydrocycloocta[b]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 3-Bromo-4,5,6,7-tetrahydro-1-benzothiophene-2-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page

6,7-Dihydro-4-benzo[b]thiophenone is a synthetic flavonoid that has been shown to be effective in the treatment of cancer cells. It binds to the oxytocin receptor and quinoline derivatives, inhibiting topoisomerase II and IV. This drug also inhibits the production of cancer cells by catalysing reactions involving piperazine and chloride. 6,7-Dihydro-4-benzo[b]thiophenone has been shown to have antimicrobial properties against bacteria such as Staphylococcus aureus, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Salmonella typhimurium.

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Please enquire for more information about Ethyl 2-[(2-bromobutanoyl)amino]-5,6,7,8-tetrahydro-4H-cyclohepta[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 Propyl 2-amino-5,6-dihydro-4H-cyclopenta[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 3-[(chloroacetyl)amino]thiophene-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 2,4-Dimethylthiophene is a biochemical used for proteomics and food research. References Xu, Q. et al.: Food Res. Int., 54, 683 (2013);

2-tert-Butylthiophene is an isomer of thiophene that has been used as a ligand in photochemical reactions. It has also been used in the synthesis of other organic compounds, such as arenes and chlorides. 2-tert-Butylthiophene is a proton acceptor and can be used to sensitize photoelectron spectroscopy. It has been shown to have the ability to convert solar energy into electrical energy when paired with a catalyst, such as boron trifluoride etherate. 2-tert-Butylthiophene can also be used for x-ray crystallography studies of chloride and hydrogen chloride molecules.

Please enquire for more information about Propyl 2-amino-5-methyl-4-phenylthiophene-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 6-tert-Butyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carbohydrazide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2,3-Dibromo-4,5,6,7-tetrahydro-1-benzothiophene 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-6-ethyl-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

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

5-Bromo-2-thiopheneboronic acid is a boronic acid that can be used for cross-coupling reactions. It has inhibitory properties and can be used to synthesize 4-fluorophenylboronic acid, which is an intermediate of the Suzuki reaction. This product may also be used in the synthesis of boronic acids, which are inhibitors of hormone-sensitive lipase. 5-Bromo-2-thiopheneboronic acid is a chloride salt that does not need to be purified before use. The chloride anion can act as a nucleophile in cross coupling reactions with organoboron compounds or organosilanes. 5-Bromo-2-thiopheneboronic acid also has the ability to inhibit lipid enzymes such as lipase and phospholipase A2 through its ability to bind to and inhibit these enzymes' active sites.

Please enquire for more information about 2-Amino-6-methyl-N-(pyridin-3-ylmethyl)-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 Methyl 2-isothiocyanato-5-methylthiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page