Heterocycles with Sulphur (S)

Please enquire for more information about 3-Chloro-6-nitro-1-benzothiophene-2-carbonyl chloride 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-Chloro-1-benzothiophene-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Bromo-4-methylthiophene is an organic compound that belongs to the group of isomeric, cyclic, and single-stranded compounds. It has a transition state with a single electron in the highest occupied molecular orbital (HOMO). 3-Bromo-4-methylthiophene has been shown to undergo chemical reactions with azobenzene, which are excimer molecules that can be used as optical switches in photonic devices. The absorption spectroscopy and voltammetry of 3-bromo-4-methylthiophene have been studied for their photophysical properties.

3-Chlorobenzo[b]thiophene-2-carboxylic acid is a novel aminothiophene compound that inhibits the activity of DNA repair enzymes. It has been shown to be cytotoxic in cancer cells, with a high level of selectivity for non-small cell lung cancer. 3-Chlorobenzo[b]thiophene-2-carboxylic acid binds to the DNA repair enzyme Mcl-1 and prevents it from binding to DNA. This prevents the enzyme from repairing damaged DNA, leading to apoptosis and cell death. This drug has also been shown to inhibit homologous recombination in vitro and in vivo, which is an important pathway for DNA repair.

Please enquire for more information about 5-Formyl-2-[(2-nitrophenyl)amino]-3-cyanothiophene 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-(4-chlorophenyl)-6-methyl-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 3-Acetyl-2-(methylaminosulfonyl)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 Methyl 5-amino-4-cyano-3-(2-methoxy-2-oxoethyl)thiophene-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 5-(Ethoxycarbonyl)thiophene-3-boronic Acid is a useful reagent for preparing hydroxyimino(phenyl)propanones as GPBAR1 agonists. References Bissantz, C., et al.: U.S. Pat. Appl. Publ. (2012), US 20120010190 A1

Dibenzothiophene-2-ol is an extracellular metabolite that is produced by the oxidation of sulfides, thiols, or disulfides. It has been shown to have a chromatographic profile that matches that of chromene, which is oxidized by x-ray absorption to give sulfoxide and then hydrolyzed to give dibenzothiophene-2-ol. This heterocycle undergoes oxidation with peroxide or hydrogen peroxide to produce an array of products with different chromatographic profiles. Dibenzothiophene-2-ol can be quantified using analytical methods such as gas chromatography and mass spectrometry.

Applications Ethyl 2-Aminothiophene-3-carboxylate (cas# 31891-06-2) is a compound useful in organic synthesis.

Please enquire for more information about Methyl 2-isothiocyanato-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 rac-N-(1,2,3,4-tetrahydro-5-methoxy-2-naphthalenyl)-2-thiopheneethanamine hydrochloride 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-(1-naphthyl)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-[(chloroacetyl)amino]-5-ethylthiophene-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-tert-butylphenyl)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 6-bromobenzo[b]thiophene-2-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-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 3-Hydroxy-5-(Trifluoromethyl)-2-Thiophenecarboxylic 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 3-(Pyridine-2-carbonyl)-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

Please enquire for more information about N-(2,5-dimethylphenyl)(3-chlorobenzo[b]thiophen-2-yl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Bromo-3-octylthiophene is a molecule that has been studied for its potential use in electrochemical polymerization and as a functional theory. This compound is chiral, with the two enantiomers having different properties. One of the enantiomers has been shown to be more reactive than the other, which may be due to it being more soluble. The photophysical properties of 2-bromo-3-octylthiophene have also been investigated and optimized to enhance their fluorescence and light emission. The ligand on this molecule can bind metal ions, such as palladium, which can be used in catalysis reactions to form metal complexes. 2-Bromo-3-octylthiophene also has transport properties that are dependent on its morphology and voltammetry. It can act as an acceptor in devices such as solar cells or organic light emitting diodes (OLEDs).

(6α,11β,16α,17α)-6,9-Difluoro-11-hydroxy-16-methyl-spiro[androsta-1,4-diene-17,5'-[1,3]oxathiolane]-2',3,4'-trione is a fine chemical that can be used as a building block for the synthesis of complex compounds. This compound is also useful as a reagent and specialty chemical. (6α,11β,16α,17α)-6,9-Difluoro-11-hydroxy-16-methyl spiro[androsta-1,4 diene 17.beta., 5'(1'3'oxathiolane)] 2',3',4'-trione has been shown to be an excellent intermediate for organic reactions and may be used as a scaffold in drug design.

Applications Benzo[b]thiophen-2(3H)-one is a reactant used in the synthesis of merocyanines dyes. References Glauert, R. & Mann, F.: J. Chem. Soc., 5012 (1952)

Please enquire for more information about Methyl 2-isothiocyanato-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 5-(4-Bromophenyl)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,N-dimethyl-1-benzothiophene-2-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

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3-Butylthiophene is a crystalline polymorph that can be obtained by polymerizing 3-butylthiophene with different concentrations of the polymer. This material has been shown to have a metastable phase, which means it will eventually convert to another form. 3-Butylthiophene has optical properties that are dependent on the morphology of the film, such as absorption and fluorescence. The water absorption is also dependent on the morphology of the film. The crystal structure of 3-butylthiophene is made up of molecules in a hexagonal pattern. The reaction time for this molecule depends on the solvent used for synthesis, as well as its concentration.

Please enquire for more information about Ethyl 3-amino-5-(3-nitrophenyl)thiophene-2-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-Cyclohexylthiophene-2-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Bromothiophene-2-carbonylchloride is a chemical compound with the molecular formula CHBrCl. It is a colorless liquid that reacts with water to produce hydrogen bromide and hydrobromic acid. 3-Bromothiophene-2-carbonylchloride has been used in the synthesis of alkynes, terminal alkynes, acetylenes, amines and other organic compounds. The reaction mechanism of this compound is based on nucleophilic substitution. In this process, the nucleophile attacks the electrophilic carbon atom in 3-bromothiophene-2-carbonylchloride to form an intermediate carbocation which then reacts with another molecule of ammonium chloride. This reaction can be done using two different types of bases: triethylamine or diisopropyl amine.

2-Amino-4,5-dimethylthiophene-3-carbonitrile is an antimicrobial agent that belongs to the group of hydrazines. It has a potent activity against bacteria such as methicillin resistant Staphylococcus aureus (MRSA) and Clostridium perfringens. 2-Amino-4,5-dimethylthiophene-3-carbonitrile also has an inhibitory effect on the synthesis of pyrimidines in bacteria by inhibiting the enzyme formamidopyrimidine ribonucleotide synthetase. The compound can be used in combination with chlorine or chlorinated solvents to produce formic acid, which is bactericidal against bacteria. 2-Amino-4,5-dimethylthiophene-3-carbonitrile has been shown to have antimicrobial activity against Gram negative and Gram positive organisms.

Please enquire for more information about N,N-Dimethyl-5-nitro-1-benzothiophene-2-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

a-Septithiophene is a synthetic compound that is used in the diagnosis of prostate cancer. It has been shown to be a potent inhibitor of platelet-derived growth factor (PDGF) and insulin sensitivity, and also inhibits the serine protease activity of proteinase 3 and aminopeptidase N. a-Septithiophene has also been shown to be an antagonist of the amp-activated protein kinase, which regulates glucose metabolism. The drug crystallizes as two different polymorphs: one with a melting point of 142°C and another with a melting point of 150°C. A single crystal X-ray diffraction study has shown that these two forms are distinct molecules with different molecular structures.

Please enquire for more information about N-(4-Acetylphenyl)-3-methylthiophene-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 Methyl 2-[(chloroacetyl)amino]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-cyclohexylphenyl)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 2-Amino-N-(4-chlorophenyl)-6-(1,1-dimethylpropyl)-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-Bromoacetylamino-3-(2-chlorobenzoyl)-5-(2-carbomethoxyethyl)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 Methyl 4-methoxythiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Methyl Thiophene-3-carboxylate is an organic compound that is a member of the molecule class. It has been shown to have inhibitory activity against the acceptor in a solar cell as well as against the aromatic hydrocarbon in a profile experiment. Methyl Thiophene-3-carboxylate has also been shown to have cytotoxic activity in vitro and has been used as a model for studying conformational changes of organic molecules. Methyl Thiophene-3-carboxylate can be used in coordination chemistry, such as with substrates or catalysts, to form homogeneous mixtures. It also shows morphology properties that are similar to those seen in vivo.

3-Bromothiophene-2-carboxylic acid is a synthetic compound that has the chemical formula CHBrO. It is a colorless crystalline solid. 3-Bromothiophene-2-carboxylic acid is used in the synthesis of other organic compounds and as a precursor to dyes, pharmaceuticals, and pesticides. 3-Bromothiophene-2-carboxylic acid has antireflection properties that make it useful for coatings on optical devices such as lenses and windows.

Please enquire for more information about Methyl 2-amino-5-pentyl-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 Isopropyl 2-amino-4-(2-chlorophenyl)thiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 6,6-Dimethyl-3-(Methylthio)-4-Oxo-4,5,6,7-Tetrahydrobenzo[C]Thiophene-1-Carbonitrile (cas# 175202-50-3) is a useful research chemical.

2-Aminothiophene-3-methyl carboxylate is a hydrogen bond that is derived from the amino acid methionine. It has been shown to have potent antitumor activity and can be used for the treatment of cancer. 2-Aminothiophene-3-methyl carboxylate has a molecular weight of 244.6 g/mol, an isolated yield of 0.68%, and a melting point of 245 °C.

Applications Tetrachlorothiophene is chlorinated derivative of Thiophene (T368080), which is used as a building block of various organic molecules and pharmaceuticals providing functional properties. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Prasad, B. et al.: Chem. Comm., 48, 10434 (2012); Freitas, V. et al.: Struct. Chem., 24, 661 (2013);

Please enquire for more information about 4-Cyano-5-[(cyanoacetyl)amino]-N,N,3-trimethylthiophene-2-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-(Trifluoromethyl)thiophenylhydrazine hydrochloride (TFTH) is a chemical compound that belongs to the group of useful scaffolds, versatile building blocks, and reaction components. It has been used as a research chemical in the synthesis of complex compounds with high quality and is an intermediate for speciality chemicals. TFTH can be used as a reagent in organic chemistry for the preparation of amines and amino alcohols. This compound has CAS No. 162258-86-8.br>br> 4-(Trifluoromethyl)thiophenylhydrazine hydrochloride has been shown to be an excellent building block in organic synthesis because it is stable under mild conditions, reacts rapidly with nucleophiles, and is readily available from commercial sources.

Please enquire for more information about 3,7-Dichloro-6-methoxy-1-benzothiophene-2-carbonyl chloride 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 Methyl 2-[(chloroacetyl)amino]-4-(4-methylphenyl)thiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Methyl 4-aminothiophene-3-carboxylate is a section compound that is used to synthesize 5-hydroxytryptamine (5-HT) analogs. It has been shown to have selective agonistic activity at the 5-HT1A receptor in fibroblast cells and can be used in cancer research. Methyl 4-aminothiophene-3-carboxylate is an imine that can undergo photolysis to form an electron and a positive charge. The photophysical properties of this molecule have been studied by measuring its absorption spectrum and fluorescence emission spectrum. This analog can also react with nucleosides to form deoxyribonucleosides, which are widely used as anticancer agents. Methyl 4-aminothiophene-3-carboxylate reacts with chloride ions to form a carbocation, which may be responsible for its biological activity.

2-[(2-Nitrophenyl)amino]-3-cyanothiophene is a yellow crystalline solid that belongs to the nitrophenyl compounds. The solubility of this compound in water is relatively high, but it can be dissolved in concentrated hydrochloric acid and sulfuric acid. It has a melting point of 115°C and decomposes at 210°C. 2-[(2-Nitrophenyl)amino]-3-cyanothiophene has been shown to have a transition temperature of -11°C and an equilibrium constant of 0.84 at 25°C in acetonitrile. This compound forms orange crystals when heated to 250°C for 48 hours, which are unstable under ambient conditions. 2-[(2-Nitrophenyl)amino]-3-cyanothiophene can be synthesized by heating 2-(nitrobenzene)ethanol with thiourea or cyanamide at

Ethyl 2-amino-5-methylthiophene-3-carboxylate (EMTC) is a nonclassical amide that has been shown to be a potential antitumor agent. EMTC inhibits tumor growth by activating gene expression and inducing apoptosis in cancer cells. It inhibits the synthesis of DNA, RNA, and proteins in tumor cells, leading to cell death. EMTC also inhibits the production of pyrimidine derivatives and thymidylate in cells. The x-ray crystal structures of EMTC have been determined, which may allow for the development of new drugs with similar activity.

Please enquire for more information about 5-(Bromomethyl)thiophene-2-carbonitrile 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 3-{4H,5H,6H-Cyclopenta[b]thiophen-2-yl}-4-methyl-1-phenyl-1H-pyrazol-5-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page

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