Heterociclos con azufre (S)

Please enquire for more information about 1-Chloronaphtho[2,1-b]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 4-Ethyl 2-methyl 5-amino-3-methylthiophene-2,4-dicarboxylate 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-chloro-5-nitrophenyl)-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

4-Chlorotetrahydrothiophene-3-ol 1,1-dioxide is a nucleophilic reagent that is used in organic synthesis. It reacts with electron-deficient alkylating agents to form mixed alkyl chlorides. 4-Chlorotetrahydrothiophene-3-ol 1,1-dioxide has an optimum reaction temperature of -78 degrees Celsius and can react with a wide range of electron rich and electron deficient groups. This compound is a white solid at room temperature.

Please enquire for more information about 2-Amino-6-methyl-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 2-Bromo-3-butylthiophene 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-5-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 4-Methylthiophene-2-boronic 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-(4-methylbenzyl)-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

Ethyl 2-methylthiophene-3-carboxylate is an intermediate in the synthesis of a variety of organic compounds, including fluoroalcohols and pharmaceuticals. The synthesis is based on the Wittig reaction, which involves the formation of a wittig reagent from a magnesium halide and a carboxylic acid chloride. This reagent reacts with an aromatic compound such as thiophene to form an alkyl group at the α position. The alkylation proceeds intramolecularly to form ethyl 2-methylthiophene-3-carboxylate without any need for an external base. Ethyl 2-methylthiophene-3-carboxylate can be obtained through a scalable, efficient method that uses Grignard reagents as starting materials.

Please enquire for more information about methyl 3-(((4,4-dimethyl-2,6-dioxocyclohexylidene)methyl)amino)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 Methyl 2-amino-4-(4-isobutylphenyl)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-tert-Butyl 4-ethyl 5-amino-3-methylthiophene-2,4-dicarboxylate 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-(4-methylphenyl)thiophene-3-carboxamide including the price, delivery time and more detailed product information at the technical inquiry form on this page