Heterocycles with Sulphur (S)

Please enquire for more information about Isopropyl 2-amino-4-(4-ethylphenyl)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-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

Please enquire for more information about 2-Amino-6-phenyl-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-[(cyanoacetyl)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 Methyl 2-amino-4-isopropylthiophene-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 2-amino-4-(2,4-dimethylphenyl)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 Isopropyl 2-amino-4-(3,4-dimethylphenyl)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-6-tert-butyl-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 Dimethyl 5-isothiocyanato-3-methylthiophene-2,4-dicarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Phenylthiophene is a diazonium salt that reacts with hydroxyl groups to form diazo compounds. It has been used in the Suzuki coupling reaction to create a wide range of products, including pharmaceuticals and agrochemicals. 2-Phenylthiophene has been shown to have anti-cancer properties, inhibiting cervical cancer cell growth and inducing apoptosis. 2-Phenylthiophene also appears to have anti-inflammatory properties and may be useful in treating inflammatory bowel disease.

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

5-Ethylthiophene-2-carboxylic acid is a chemical compound that has been acetylated. It is often used as an intermediate in organic synthesis, especially as a building block for the production of pharmaceuticals and agrochemicals. 5-Ethylthiophene-2-carboxylic acid can be chromatographically separated by using strategies such as validation, algorithm, and regression. The chemical structure of this compound may be determined by using methods such as fingerprinting and gas chromatography. The structural isomers of this compound are naphthenic (5E) and butyllithium (5B). Chemists use 5E and 5B to profile the properties of this substance.

Methyl3-iodothiophene-2-carboxylate is a chemical compound that is involved in the biosynthesis of eicosanoids. It can be synthesized by the cyclization of the corresponding lactam to produce an intermediate, which is then converted to methyl3-iodothiophene-2-carboxylate by hydrolysis or reduction. This compound has been shown to inhibit malaria parasites such as Plasmodium falciparum and Plasmodium vivax. Methyl3-iodothiophene-2-carboxylate also inhibits the growth of bacteria such as Staphylococcus aureus and Bacillus subtilis. The mechanism of action is believed to be due to its ability to inhibit protein synthesis by binding with ribosomes in prokaryotic cells.END>

2,5-Dibromo-3-n-octylthiophene is a soluble and efficient solar cell polymer. It has been shown to have high efficiency in the transformation of light into electricity. This polymer is easy to synthesize and can be used to make organic solar cells. The polymer was found to be photoactive and able to generate photocurrents in response to irradiation with UV light at wavelength 254 nm. It has also been shown that this polymer can be transformed efficiently by imidazole when it is exposed to light with a wavelength of 365 nm.

Please enquire for more information about 2-Amino-6-ethyl-N-(4-methylbenzyl)-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-[(chloroacetyl)amino]-4-(2,5-dimethylphenyl)thiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Acetyl-3-chlorothiophene is a catalyst that is used in the arylation of aromatic compounds. It has been shown to catalyze the reaction between an aryl bromide and an arylated thiophene, leading to high yields of the desired product. This catalyst can be used for the synthesis of polyfunctionalized thiophenes with high yields. 2-Acetyl-3-chlorothiophene has also been shown to be effective in catalyzing the reaction between aryl bromides and functionalized thiophenes, leading to high yields of the desired product.

Please enquire for more information about Ethyl 2-amino-4-(4-tert-butylphenyl)-5-methylthiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Methylthiophene-2-carbonyl chloride is a chemical compound with the molecular formula C6H5CH(COCl)CH3. It is used as an intermediate in organic synthesis, mainly for the production of pharmaceuticals. The molecule consists of a methyl group attached to a thiophene ring and two carbonyl groups. 5-Methylthiophene-2-carbonyl chloride is a colorless liquid that is soluble in water and acetone. It is highly reactive, which makes it useful for the preparation of other molecules. The reactivity of 5-methylthiophene-2-carbonyl chloride can be explained by its ability to undergo both dehydrogenation and transfer reactions. These reactions are catalyzed by nucleophilic compounds such as water or alcohols, which provide hydroxyl ions or hydrogen atoms respectively. In addition, this compound can be photolyzed with irradiation to form singlet oxygen (1O

Please enquire for more information about (5-(Hydroxymethyl)thiophen-2-yl)boronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Ethyl 2-amino-5-ethylthiophene-3-carboxylate is a nonclassical alkylating agent that inhibits cancer cell proliferation and has shown tumor inhibition in colon cancer cells. It is synthesized from ethyl acetoacetate and glutamic acid diethyl ester. This compound binds to the thymidylate synthetase enzyme, which is involved in DNA synthesis, and prevents it from functioning. Taxol, a drug used for the treatment of cancer, also binds to this enzyme and inhibits its function. The average age of patients with colon cancer was found to be 54 years old. This drug has been shown to bind to X-ray crystal structures of tumor cells from all major histological types.

Please enquire for more information about 2-Amino-N-benzyl-6-tert-amyl-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-N-(1-phenylethyl)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 Ethyl 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

Please enquire for more information about Methyl 2-[(chloroacetyl)amino]-4-ethyl-5-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-(Methoxymethyl)thiophene-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 6-tert-Butyl-1-benzothiophene-3-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 4-(2,5-Dichlorothiophen-3-yl)-1,3-thiazol-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 2,5-Dichlorothiophene-3-sulfonylchloride 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 3-amino-5-(3-chlorophenyl)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 Methyl3-amino-5-(4-chlorophenyl)thiophene-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Phenylthiourea is a heterocyclic compound that can be synthesized by the oxidation of 4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylic acid. This compound has been shown to inhibit tyrosinase activity in animals and may be useful in the prophylaxis and/or treatment of erectile dysfunction or other diseases related to sexual dysfunction. Phenylthiourea also inhibits diphenolase activity and is thereby an inhibitor of phenol degradation. Phenylthiourea is used as a reagent for the detection of phenolase enzymes. It has been shown to inhibit some bacteria, including Mycobacterium tuberculosis, but not others such as Staphylococcus aureus.

Please enquire for more information about Propyl 2-amino-4-(4-methoxyphenyl)-5-methylthiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications (S)-3-(Allyl(methyl)amino)-1-(thiophen-2-yl)propan-1-ol is an intermediate in the syntehsis of 4-Hydroxy Duloxetine β-D-Glucuronide Sodium Salt (H941805), which is a metabolite of Duloxetine. References Lantz, R.J., et al.: Drug Dispos. Metab., 31, 1142 (2003); Detke, M., et al.: J. Clin Psy., 63, 308 (2002); Bymaster, F.P., et al.: Bioorg. Med., Chem. Lett., 13, 4477 (2003);

Please enquire for more information about 6-(1,1-Dimethylpropyl)-4,5,6,7-tetrahydro-1-benzothiophene-3-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 3-Chloro-4-methyl-1-benzothiophene-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 1,3-Dibromo-benzo[c]thiophenen 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-methoxyphenyl)-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 Methyl 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

Please enquire for more information about 2-Amino-N-cyclohexyl-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-(5-Methylthiophen-2-yl)-2-(morpholin-4-yl)ethan-1-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-(2-Methoxyphenoxy)ethyl]thiophene-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 4-Bromo-5-methylthiophene-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 Ethyl 2-amino-4-(2,5-dimethylphenyl)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-(2-furylmethyl)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 5-((4-Boc-piperazine)Methyl)-2-thiopheneboronic acid pinacol ester 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-cyclopentyl-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

4,5-Dichlorothiophene-2-carboxylic acid is an industrial chemical that is used in the chlorination of organic compounds. It is also useful for esterification reactions. This compound has a high selectivity for chlorination and can be used to efficiently convert alcohols to alkyl chlorides. 4,5-Dichlorothiophene-2-carboxylic acid can also be used in the hydrolysis of esters. The reaction is operational at room temperature and the product can be isolated through crystallization or distillation.

Benzo[b]thiophen-4-amine (BTA) is a yellow solid that is soluble in organic solvents. BTA can be synthesized from formic acid and piperazine. The major impurities of BTA are quinones, which can be removed by photolysis. Hydrogen peroxide is produced during the synthesis of BTA and can be used as a catalyst for the reaction. The solvents used to extract BTA are not well characterized, but may include solvents such as chloroform, benzene, or carbon tetrachloride. BTA is used in the manufacture of polyphosphoric acid and nucleophilic reagents such as sodium thiocyanate. Unidentified substances were also found in the crude product of this chemical’s synthesis, which may have been formed during the process. Recombinant human proteins have been made with this chemical.br>br> BETA-

Please enquire for more information about Propyl 2-amino-4,5,6,7,8,9,10,11,12,13-decahydrocyclododeca[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 5-[(chloroacetyl)amino]-4-cyano-3-methylthiophene-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 2-Amino-N-(aminocarbonyl)thiophene-3-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Thiopheneethanol tosylate (2TEtOS) is an antitubercular agent that belongs to the class of thiopheneethanol esters. It is a potent inhibitor of Mycobacterium tuberculosis and other bacteria by blocking the transfer reactions that are required for bacterial growth. The molecular structure of 2TEtOS consists of a thiophene ring with an allyl group attached to it and a chiral sulfur atom in the center. This molecule can be derivatized with various ligands, which enables the control experiments to be performed. 2TEtOS has been shown to have redox potentials and diffraction properties that are similar to those of borohydride reduction agents, suggesting that 2TEtOS may also act as a reducing agent.

Please enquire for more information about Isopropyl 2-amino-4-methyl-5-{[(2-methylphenyl)amino]carbonyl}thiophene-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Ethynylthiophene is a catalyst that has been used to hydrogenate aliphatic and aromatic compounds. It has significant cytotoxicity, which may be due to its ability to transport electrons. 3-Ethynylthiophene is also a photochemical molecule that can transfer the energy of light onto the substrate, which makes it an efficient method for producing polymerized products. 3-Ethynylthiophene has been shown to be a low energy molecule with structural analysis that can be used in the development of new drugs for cancer treatments.

2-Chloro-5-methylthiophene is an organic compound with a boronic acid group that allows cross-coupling reactions. This compound can be used as a building block for the synthesis of other boronate derivatives. It has been shown to react with amines in an acidic environment and can form stable molecules, which may have structural properties that are different from those of the original molecule. 2-Chloro-5-methylthiophene has been synthesized using X-ray crystal structures and spectroscopy techniques, which show its fluorescence properties. This compound also exhibits linker photochromism and cross-coupling functional groups.

Methyl 5-methylthiophene-2-carboxylate is a reagent that has been used to introduce a sulfur atom into organic compounds. It reacts with molybdenum and carbon tetrachloride to produce methyl 5-methylthiophene-2-sulfonyl chloride, which can be hydrolyzed to form the corresponding thiophene carboxylic acid. The at1 receptor antagonist properties of this compound were first demonstrated in the late 1980s when it was found that it can block the action of angiotensin II by binding to AT1 receptors. This reaction scheme also includes an alcoholysis step, which converts methyl 5-methylthiophene-2-carboxylate into selenophene and carbon tetrachloride.

2,5-Dibromo-3-dodecylthiophene is a polymerization agent that is used in the preparation of polymers. It is a cross-coupling agent that reacts with an alcohol (generally methanol or ethanol) to form a symmetric alcohol. This reaction takes place in the presence of a base such as sodium ethoxide in an inert solvent such as tetrahydrofuran. The 2,5-dibromo-3-dodecylthiophene can be prepared by reacting hexane and chloroform with magnesium and bromine. The reaction takes place at high temperature (150°C). The resultant product is then filtered from the reaction mixture and purified by evaporative distillation or by recrystallization from hexane or chloroform.

Please enquire for more information about 2-Methyl-1,3-oxathiolane-2-ethanethiol including the price, delivery time and more detailed product information at the technical inquiry form on this page