Hétérocycles soufrés (S)

Please enquire for more information about N-(2-Thiophenesulfonyl)-L-prolinamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Phenyl-[5-(4,4,5,5-tetraMethyl-[1,3,2]dioxaborolan-2-yl)-thiophen-2-ylMethylene]-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 2-Amino-6-propyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonitrile 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-6-methyl-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

6-Bromo-3-chloro-1-benzothiophene-2-carbonyl chloride is a synthetic dyestuff that can be used in the production of textile fibers, dyestuffs, and paints. It is soluble in water and fats, but insoluble in hydrocarbons. The compound is synthesized by reacting 6-bromo-3-chlorobenzothiophene with an acid chloride followed by heating to produce a red dye. This dye has been shown to be resistant to light and heat and has low toxicity.

Diethyl 5-amino-3-methyl-2,4-thiophenedicarboxylate is a chemical compound belonging to the group of thiophenedicarboxylic acid derivatives. It is a white crystalline solid that is soluble in water and alcohol. The molecular weight of diethyl 5-amino-3-methyl-2,4-thiophenedicarboxylate is 186.19 g/mol and it has an electronegativity of 2.1. Diethyl 5-amino-3-methyl-2,4-thiophenedicarboxylate can be used as a raw material for the production of cellulose acetate, polyesters, and other organic compounds with a molecular formula C5H7NO5S.

4-(4-Chlorophenyl)-1-[3-[2-(4-Fluorophenyl)-1,3-dithiolan-2-yl]propyl]piperidin-4-ol is a potent and selective inhibitor of the human epidermal growth factor receptor 2 (HER2) that blocks the activation of the epidermal growth factor receptor. It has a molecular weight of 514.44 and a calculated radius of 3.67 Å. 4-(4-Chlorophenyl)-1-[3-[2-(4-fluorophenyl)-1,3-dithiolan-2-yl]propyl]piperidin-4-ol binds to the nucleotide binding site on HER2, preventing phosphorylation by protein kinase A and protein kinase B. This inhibition leads to reduced downstream signalling for cell proliferation, differentiation, and survival. This compound also inhibits the production of the "pro"

Please enquire for more information about Methyl 3-[(cyclohexylamino)sulfonyl]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 4-(1,2-Dithiolan-3-yl)butanoic 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 Methyl 2-amino-4-methyl-5-[(propylamino)carbonyl]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-Methyl-4,5,6,7-tetrahydro-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 Morpholin-4-yl-thiophen-2-yl-acetic 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 Methyl 2-[(3-chloropropanoyl)amino]-6-phenyl-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 N-(4-Acetylphenyl)-4,5-dimethylthiophene-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 4-Bromo-3-chloro-1-benzothiophene-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-BroMo-3-Dodecylthiophene is a chemical compound that has been investigated for its use in designing new types of semiconducting polymers. It is insoluble and can be used as a polymer for transport properties. In addition, it has been used to synthesize supramolecular structures with transition metal ions, such as Fe2+ and Cu2+. 2-BroMo-3-Dodecylthiophene has been shown to have photophysical properties that are dependent on the crystalline structure of the molecule. The diethyl ester form exhibits blue fluorescence with an emission maximum at 486 nm, while the crystalline form emits red fluorescence with an emission maximum at 604 nm. These differences are due to the presence of metal ion complexes in the crystal lattice that increase the electron density near the thiophene ring. The compound also shows high chemical stability with no detectable decomposition after three months in air or moisture.

Please enquire for more information about Methyl 2-isothiocyanato-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 5-Bromo-N-ethylthiophene-2-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Bromo-4-formylthiophene is a monolayer that can be synthesized by electrochemical polymerization. It has been shown to have a high degree of crystallinity and low volatility. 3-Bromo-4-formylthiophene is stable in the solid phase and can be used as an acceptor in organic light emitting diodes (OLEDs). The photophysical properties of this molecule are dependent on temperature, with the lowest energy emission occurring at lower temperatures. This molecule has also been studied for its use in electrochemical devices such as fuel cells, electrolyzers, and batteries.

Please enquire for more information about Methyl 4,5-diaminothiophene-2-carboxylate 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 2-Amino-N-(3-chlorophenyl)-4-ethyl-5-methylthiophene-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 Amino-(5-methyl-thiophen-2-yl)-aceticacid including the price, delivery time and more detailed product information at the technical inquiry form on this page

(6R,7R)-3-(Acetoxymethyl)-8-oxo-7-(2-(thiophen-2-yl)acetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid is an antimicrobial agent that inhibits bacterial growth by binding to the penicillin binding protein (PBP), which prevents the synthesis of peptidoglycan. This drug has shown effectiveness against gram positive bacteria, including aerobacter aerogenes, as well as infectious diseases in wastewater treatment plants. It has also been demonstrated to be effective in experimental models of infection due to high resistance and cell signaling pathways. The reaction solution was analyzed by plasma mass spectrometry.

Please enquire for more information about Methyl 6-tert-butyl-2-[(cyanoacetyl)amino]-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

3-Amino-2-thiophenecarboxylic acid is an antihypertensive agent that inhibits angiotensin I-converting enzyme (ACE). It has been shown to have a protective effect against cancer and to reduce locomotor activity in rodents. 3-Amino-2-thiophenecarboxylic acid is produced by the reaction of 2-aminoethanethiol with thiophenecarboxylic acid. The product is a salt, which can be obtained in acidic or alkaline solutions. This compound also inhibits replication of Trichomonas vaginalis and replicative DNA polymerases from Escherichia coli. 3-Amino-2-thiophenecarboxylic acid has been shown to have autophagy inducing properties, which may be due to its inhibition of protein synthesis.

Please enquire for more information about 5-Bromo-N-propylthiophene-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 2-Amino-4-(3,4-dimethoxyphenyl)thiophene-3-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Fluorothiophenol is a reactive chemical that can be used as a monomer for the synthesis of polymers. It has been shown to polymerize with acrylonitrile and methacrylate in the presence of an initiator to form polyacrylonitrile and polymethacrylate, respectively. 4-Fluorothiophenol reacts with unsaturated fatty acids to form thiolates, which are useful intermediates in organic synthesis. 4-Fluorothiophenol also reacts with sulfur transfer agents such as thiourea or mercaptoethanol, leading to S-sulfides that are useful intermediates in organic synthesis. These reactions can be followed by kinetic energy spectroscopy (photoelectron) and nuclear magnetic resonance spectroscopy (NMR). 4-Fluorothiophenol has been shown to undergo intramolecular hydrogen transfer reactions with second order rate constants ranging from

Please enquire for more information about 2-amino-5,6-dihydro-4h-cyclopenta[b]thiophene-3-carbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Chlorothiophene-3-carboxylic acid is a chemical reagent that is used in organic synthesis. It is soluble in organic solvents such as methyl tert-butyl ether, and can be layered with sulfuryl chloride to form a mixture that has a high boiling point. The reaction solution can be recrystallized from tert-butyl ether to produce the compound in pure form. This chemical reacts with sulfuryl chloride to produce 5-chlorothiophene-3-sulfonyl chloride, which can then be reacted with an amine to produce 5-chlorothiophene-3-amine.

Please enquire for more information about N-(3-Acetylphenyl)-5-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 Isopropyl 2-amino-5-{[(4-methoxyphenyl)amino]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 2-Amino-4,5-dimethylthiophene-3-carboxylicacid including the price, delivery time and more detailed product information at the technical inquiry form on this page