Heterocycles with Sulphur (S)

Please enquire for more information about 5'-Amino-2,3'-bithiophene-4'-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

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5-Methyl-2-thiophenecarboxylic acid is an organic compound with the molecular formula CH3COOH. It has a carboxyl group at one end and a methyl group at the other, hence its name. 5-Methyl-2-thiophenecarboxylic acid is used in the synthesis of esters that are useful as intermediates in the production of pharmaceuticals, pesticides, and other chemicals. The asymmetric synthesis of 5-Methyl-2-thiophenecarboxylic acid was accomplished by reacting it with sodium hydroxide in methanol. The compound is also found to have anticarcinogenic properties. A study conducted on mice showed that 5-Methyl-2-thiophenecarboxylic acid inhibited skin cancer by inducing apoptosis in melanoma cells and inhibiting cell proliferation. 5-Methyl-2-thiophenecarboxylic acid has been shown to

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.

Methyl 3-amino-5-phenyl-2-thiophenecarboxylate is a benzene derivative that has been shown to have natriuretic and thioglycolate cyclopentyl peptide receptor agonist activity. It is also an efficient, water soluble synthetic intermediate that can be used for the synthesis of peptides. Methyl 3-amino-5-phenyl-2-thiophenecarboxylate has been shown to have high efficiency in solvents and is synthesized with good yields.

Please enquire for more information about 5-Iodo-benzo[b]-thiophene including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Butyl 2-amino-5-(aminocarbonyl)-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 5-Methylbenzo[b]thiophene-2-boronicacid 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-benzyl-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 3-(Thiophen-2-yl)-1,2,4-thiadiazol-5-amine 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-4-phenylthiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

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4-Chlorothiophene-2-carboxaldehyde is an organic compound that has the chemical formula C6H4ClO. This compound is a colorless liquid with a fruity odor. It is used in the synthesis of many drugs and dyes, as well as in the preparation of pesticides. 4-Chlorothiophene-2-carboxaldehyde is also used for fluorescence microscopy and elemental analysis. 4-Chlorothiophene-2-carboxaldehyde can be recycled by reacting it with sodium hydroxide to produce thiophane, which can then be converted back to chlorothiophene by hydrolysis with sulfuric acid. The yield of this reaction depends on how much water was present during the initial reaction; higher yields are obtained when less water was present. 4-Chlorothiophene-2-carboxaldehyde can also be purified by filtration after it has been dissolved in a solvent such as chloro

Ethyl 2-amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate is an antibacterial agent that inhibits the growth of bacteria by binding to amines and metal ions. It also has in vitro anticancer activity against cancer cells. Ethyl 2-amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate has been shown to have antiinflammatory activity in rats.

3-Acetyl-2-(aminosulfonyl)-5-chlorothiophene is a ketone that was synthesized to inhibit the enzyme carbonic anhydrase. 3-Acetyl-2-(aminosulfonyl)-5-chlorothiophene has been shown to be enantioselective, which means it is more active against one form of the enzyme than another. It is also brominated and has a thioether group. This compound inhibits carbonic anhydrase by binding to the active site of the enzyme, preventing the formation of carbonic acid from bicarbonate and hydrogen ions. 3-Acetyl-2-(aminosulfonyl)-5-chlorothiophene has been shown in research studies to be a chloride ionizable and hydroxylamine alkylation inhibitor. It also has bromohydrin and tosylation properties, as well as anti-inflammatory activities.

Please enquire for more information about Methyl 2-amino-5-(1-phenylethyl)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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5-Amino-1-benzothiophene-2-carboxylic acid (5ABTC) is a heterocyclic amine that has potent anti-inflammatory activity. 5ABTC prevents the production of inflammatory prostaglandin E2 by inhibiting cyclooxygenase and lipoxygenase activities. It also inhibits the production of proinflammatory cytokines, such as tumor necrosis factor alpha (TNFα), interleukin 1β (IL1β), and IL6. 5ABTC is not cytotoxic to cells in vitro and has been shown to be safe in vivo. The compound's anti-inflammatory effects are due to its ability to inhibit the synthesis of arachidonic acid, which is an important precursor for proinflammatory signaling pathways.

4-Bromothiophene-3-carboxylic acid is a heterocyclic compound that can be found in many different isomeric forms. This compound has been shown to inhibit the growth of cancer cells, and it also inhibits the activity of ring-opening dioxygenases by binding to their heme cofactor. 4-Bromothiophene-3-carboxylic acid is a potent inhibitor of acidic phosphatases, and it also inhibits polyphosphoric acid reductases. It is an inhibitor of homophthalate dioxygenase and nitrate reductase due to its ability to bind to their heme cofactors. The chloride salt of 4-bromothiophene-3 carboxylic acid has been shown to be a potent inhibitor of damaged DNA, as well as 3-aminobenzamide and nitrate reductases.

Thiophene-2-carbothioamide is a hydrodynamic antibacterial agent that was found to be cytotoxic for human colon carcinoma cells. It has been shown to be an acceptor and a dipole, which can form an intercalative complex with DNA, inhibiting the replication of bacterial DNA. This compound also has physicochemical properties that make it suitable as a solute in pharmaceutical products. Thiophene-2-carbothioamide is also able to bind amine groups on proteins and enzymes, which may help to explain its cytotoxicity. The fluorescence of this compound has been analysed using UV/Vis spectroscopy and found to be primary amines. nowiki> /nowiki>

2-Bromo-5-chlorothiophene is a chemical substance that has been used in the synthesis of other substances. It is commonly used to form a pyridine complex with methyl alcohol, which can be used as a Grignard reagent. 2-Bromo-5-chlorothiophene can also be used to generate dimethylformamide, which can be used as a solvent in the production of polymers. The toxicity of 2-bromo-5-chlorothiophene has been studied extensively and it has been determined that it is not toxic to humans at concentrations up to 1g/kg body weight. 2-Bromo-5-chlorothiophene is also useful in the synthesis of chemical substances by means of electrolysis and chlorine gas. The reaction selectivity for 2 bromo 5 chlorothiophene is high and it is catalyzed by kinetic energy.

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Applications Benzo[b]thiophene has application in organic as well as pharmaceutical industry as a component in the synthesis of Raloxifene, a breast cancer therapeutic, or hydrodesulfurization reactions. References Buccella, D. et al.: J. Am. Chem. Soc., 130, 16187 (2008); Gennari, L. et al.: Exp. Opin. Drug Saftey, 7, 259 (2008);

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2-Ethylhexyl 4,6-dibromo-3-fluorothieno[3,4-b]thiophene-2-carboxylate is an acceptor molecule that is used in the production of polymers for solar cells. It has a chain structure with two methyl esters. This compound can be polymerized to form a copolymer and has been shown to have high efficiency in the visible range of light. The molecule also has a wavelength range of 600 nm to 800 nm, which is ideal for polymer solar cells. 2-Ethylhexyl 4,6-dibromo-3-fluorothieno[3,4-b]thiophene-2-carboxylate is also an acid methyl ester and can be converted to the acid methyl form with strong bases such as sodium methoxide or potassium hydroxide.

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Thieno[2,3-b]thiophene is a model system that has been studied using magnetic resonance spectroscopy to identify the active methylene. It is an anticancer drug that inhibits the growth of cancer cells. Thieno[2,3-b]thiophene binds to metal carbonyls and forms a stoichiometric complex with sodium carbonate. This complex can act as a nucleophile and attack the electrophilic centers of DNA, RNA, or proteins. Thieno[2,3-b]thiophene is potent in inhibiting the activity of trifluoroacetic acid and x-ray crystal structures have shown that it has low energy requirements for binding to DNA. The electrochemical impedance spectroscopy showed that thieno[2,3-b]thiophene interacts with DNA in a time dependent manner and exhibits potent inhibition against cancer cells.

Please enquire for more information about 5-tert-Butyl-1-benzothiophene-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

3,3',5,5'-Tetrabromo-2,2'-bithiophene is a bromine-containing organic compound that has been shown to be efficient in solar cells. It has an eluting range of 1.0-1.3 and can be used as a dye in the production of perovskite crystals (a class of materials with potential applications in solar cells). 3,3',5,5'-Tetrabromo-2,2'-bithiophene has a molecular formula of C8H8Br4 and a structural formula of CHBrCH=CHBrCHBr. This macrocycle can be synthesized by reacting methylbenzene with ethynyl bromide or n-hexane with perchloric acid.

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