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Please enquire for more information about 8-Chloro-2-(3,4-dichlorophenyl)quinoline-4-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'-Isobutyl-1'-oxo-1',4'-dihydro-2'H-spiro[cyclopentane-1,3'-isoquinoline]-4'-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

6-Chloro-5-azaindole is an organic compound that is classified as a benzyl derivative. It is used as a reagent for the synthesis of other compounds and as a chemical intermediate. 6-Chloro-5-azaindole can be synthesized by reacting benzaldehyde with hydroxyl in the presence of alkali. 6-Chloro-5-azaindole can also be obtained from chlorinated benzylic alcohols, such as 6-chloro-5-(2,4,6-trimethylbenzyl)pyridine. This compound has toxic effects and should be handled with care.

Please enquire for more information about 8-Chloro-1,2,3,4-tetrahydroisoquinoline 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 tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-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 6-Methoxy-3,4-dihydroisoquinolin-1(2H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

5,7-Dinitrooxindole is an oxindole that has been synthesized by the ring-opening of hydroxylated triazoles. It has a hydrophobic character due to the presence of two nitro groups in the molecule. This compound can be used as a synthetic precursor for other compounds with biological activity. 5,7-Dinitrooxindole can be oxidized with hydroxide ions to yield 7-hydroxy-5,6-dinitrooxindole, which is an optical isomer of the molecule. The conformation of 5,7-dinitrooxindole can be transferred to other molecules using amines and cyclic sulfoxides.

3-Formyl-1H-indole-2-carboxylic acid is an organic compound that is a structural analog of indole. It can be used as a precursor in the synthesis of various heterocycles, such as indole, benzofuran and benzothiophene. 3-Formyl-1H-indole-2-carboxylic acid has low toxicity and can be used in catalytic reactions. The reactivity of 3-formylindoles is similar to that of 2,3,5,6 tetrahydrobenzo[b]thiophenes.