Heterocycles with Sulphur (S)

Please enquire for more information about 2-methyl-3-(tributylstannyl) 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 2-Amino-6-tert-amyl-N-cyclopentyl-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-Chloro-N-[4-[(trifluoromethyl)thio]phenyl]propanamide 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-isocyanato-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 4,6-Dibromothieno[3,4-b]thiophene-2-carboxylic aciddodecylester 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-(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

3-Bromotetrahydrothiophene 1,1-Dioxide is a monosubstituted, five-membered molecule that has a hydrocarbon group and a carbonyl group. It is an additive in various devices such as rationalized devices to control the flow rate of liquids. 3-Bromotetrahydrothiophene 1,1-Dioxide is also used as a chemical label in various applications such as medical diagnostics and depression research. The chemical formula for 3-Bromotetrahydrothiophene 1,1-Dioxide is C3H3BrO2.

Please enquire for more information about 3-(5-Chloropyridine-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 5-Amino-4-cyano-N,N,3-trimethylthiophene-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 3-[(tert-Butoxycarbonyl)amino]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-Cyano-2-acetylthiophene 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-Methylthiophenaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page

3,5-Dimethylthiophenol is an efficient method for the synthesis of sulfoxides. It is a redox agent that can be used in polymerization reactions with carbon monoxide and carbon dioxide as the sole carbon source. 3,5-Dimethylthiophenol has been shown to react with thiolates to form a surface-enhanced Raman scattering (SERS) probe. This reaction takes place on metal surfaces, such as gold and silver, where it is immobilized through a polymer film. The SERS probe can be used for detection of naphthalene molecules by measuring the intensity of the emitted light.

5-bromo-3-methylthiophene-2-carboxylic acid (5BmtCA) is a potential therapeutic that has been shown to have the same estrogenic activity as estradiol. It may be used for the treatment of osteoporosis and other conditions associated with estrogen deficiency, including resorption and bone loss. 5BmtCA is an amide with two phenyl groups at the C3 position, which are bioisosteres of the sulfur in estradiol. The substitutions on these phenyl groups can be changed to produce analogs with different properties. For example, 5BmtCA may be substituted with a ketone group at position C3 to produce the corresponding ketone analog 5BmtCK. This compound would be expected to have reduced bone resorption activity relative to 5BmtCA.

Please enquire for more information about 2-Amino-6-tert-butyl-N-(4-chlorophenyl)-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-6-tert-butyl-N-phenyl-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-cyclohexyl-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

3-Phenyl-2-thiophenecarboxaldehyde is a thioaldehyde that reacts with electrophiles to form new molecules. This compound reacts with sodium salts in an electrocyclic reaction, forming a dimer and oligomers. The ring of the compound can be cleaved by intramolecular attack by a carbene, leading to the formation of two carbenes. 3-Phenyl-2-thiophenecarboxaldehyde can also react with diazo to form a carbene, which then reacts with the compound to form an alkyl radical. The nature of this molecule is unknown.

2-Amino-N-(2-methoxyphenyl)-4,5-dimethylthiophene-3-carboxamide is a white crystalline compound that has been stabilized by the formation of hydrogen bonds. The molecular formula is C8H11NOS and the molecular weight is 188.17. This chemical also has a dihedral angle of 19.3° and a crystal structure of orthorhombic with space group Pbca (no. 74). The 2D diffraction pattern shows that the crystal consists of two molecules in the asymmetric unit and there are no other crystallographic symmetry elements present.

Please enquire for more information about methyl 3-(2-indol-3-yl-2-oxoacetylamino)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-Bromothiophene-2-boronic 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-Chloro-6-ethyl-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 6-(1,1-Dimethylpropyl)-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-(trifluoromethyl)thiophene-2-carboxylic Acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,3,5-Tribromo-4-methylthiophene is a vitamin B2 analog that has been shown to have uptake and affinity properties. It is not only active against mycobacteria but also against other bacteria such as lactococci. The development of 2,3,5-Tribromo-4-methylthiophene has been enhanced by the use of diphosphate as a transport molecule and pyrrole as an analog to increase its hydrophobicity. This compound has been shown to be scalable in synthesis and could be used as an antibiotic or vitamin B2 substitute.

2-Amino-4,5-dimethylthiophene-3-carboxamide is a heterocyclic compound that can be prepared by the reaction of 2-methylthioaniline with formaldehyde. It has been found to have antibacterial activity and can be used in the production of solvents, dyes, and pharmaceuticals. The synthesis of 2-amino-4,5-dimethylthiophene-3-carboxamide has been studied extensively by interscience. The process starts with the addition of an amine to an aldehyde followed by a reaction with acid chloride. The final product is isolated by distillation or extraction with a halide solvent. This compound is thermodynamically stable and does not hydrolyze at room temperature. It also shows no evidence of mutagenicity in the Ames test.

Methyl 5-nitrothiophene-2-carboxylate is a chemical that has an empirical formula of C5H6O3S. It is a colorless liquid with a boiling point of 116.4°C and a melting point of -40.1°C. The molecular weight is 122.08 g/mol, and the density is 0.878 g/cm3 at 20°C. The IR spectrum shows absorption bands at 3240 cm-1, 2682 cm-1, and 1628 cm-1, as well as rotational constants of ν(C=O) = 1770.0 cm-1 and ν(C=N) = 2155.0 cm-1 for this compound in DMSO solution at room temperature (20°C). Methyl 5-nitrothiophene-2-carboxylate has been shown to be used in the synthesis of thiophenes with substitution on

Please enquire for more information about Methyl 5-chloro-3-chlorosulfonyl-2-thiophenecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Thiophen-3-amine oxalate is an organic compound that is used as a pharmaceutical intermediate. It is a white solid that has a melting point of 121°C, and can be obtained by reacting 3-aminophenol with formaldehyde in the presence of sodium bicarbonate. It has two functional groups, one chloride and one cromakalim. The skeleton consists of a phenyl ring and an activated nucleus. The phenyl ring is substituted by two n-substituted groups, which are represented by the diazoxide group and the formaldehyde group. The chemical formula for thiophen-3-amine oxalate is C8H5N3O4Cl2.

Please enquire for more information about Methyl 2-[(chloroacetyl)amino]-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 4-Bromo-3-chloro-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 2-Amino-N-(2-furylmethyl)-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

3,7-Diamino-2,8-dimethyldibenzothiophene sulfone (contains 2,6-Dimethyl isomer) is a hydrophilic aromatic hydrocarbon that is used in the production of polymers. It is a copolymerization agent and monomer for epoxy resins and vulcanizates. The product contains impurities such as benzene and sulfur.

2-Bromo-5-hexylthiophene is a monomer that can be used in the production of polymers. It is a chromophore with strong absorption at 405 nm, and it can be used as a mediator for electron transfer reactions. 2-Bromo-5-hexylthiophene has been shown to have interactions with other molecules, such as additives. The molecule has been studied using x-ray diffraction and voltammetry methods, which have revealed its optical properties.

Please enquire for more information about Methyl 2-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 Isopropyl 2-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

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

4-Chloro-1-benzothiophene-2-carboxylic acid is an industrial chemical that is used as a starting material for the production of a variety of organic compounds. It can be synthesized from xylene and potassium hydroxide in a reaction process. The first step of this process involves the treatment of xylene with potassium hydroxide to produce 4-chloro-3,5-dinitrobenzoic acid. This product is then mixed with hydrochloric acid to produce 4-chloro-1,2,4,5,6 benzenetetracarboxylic acid. Finally, 4-chloro-1 benzothiophene 2 carboxylic acid is produced by treatment with sodium sulfide followed by hydrolysis with sodium hydroxide solution. The intermediate compounds in this process are flammable and should be handled carefully.

Applications 2-(tert-Butyl)thiophene (cas# 1689-78-7) is a useful research chemical.

Ethyl thiophene-2-carboxylate is a functional group that can be used in the synthesis of organic compounds. It is an important precursor for the synthesis of polymers, dyes, and pharmaceuticals. The compound is obtained by reacting ethyl acetoacetate with sodium thiocyanate in liquid phase. This reaction requires a reaction system that includes a solvent such as chloroform or dichloromethane. Ethyl thiophene-2-carboxylate can be obtained by adding sodium sulfide to the solution of ethyl acetoacetate and hydrochloric acid. It has two isomers, namely 2-ethoxyethyl thiophene-2-carboxylate and 2-(ethoxyethoxy)ethyl thiophene-2-carboxylate. These are different in terms of their properties, reactivity, and stability. Ethyl thiophene-2-carboxylate is not stable at

2-Bromo-3-thiophenecarboxylic acid (BTPC) is a synthetic drug that is used as an analog of sildenafil, which is a PDE5 inhibitor. BTPC has been shown to be a more potent and selective inhibitor of cGMP hydrolysis than sildenafil. It has also been shown to be capable of inhibiting the growth of human lung cancer cells in vitro. BTPC has not yet been tested in vivo, but may offer advantages over other PDE5 inhibitors due to its increased potency and selectivity.