Compuestos policíclicos

5-Fluoroquinoline is a quinoline derivative that has been shown to have tumorigenic activity in animal bioassays. In addition, 5-fluoroquinoline induced genotoxic effects in liver cells and was found to be carcinogenic in rats and mice. The mechanism of action of 5-fluoroquinoline is not yet known, but it is thought to be due to its ability to bind covalently with DNA. It also binds to RNA and protein in the cell, which may lead to inhibition of transcription or translation.

6-Aza-5-methyl-1H-indazole is a chemical compound that acts as a building block for the synthesis of pharmaceuticals and other compounds. It is used in research for the development of new drugs, such as antihypertensive agents, antibiotics, and immunosuppressants. 6-Aza-5-methyl-1H-indazole has been shown to be an effective intermediate in the synthesis of many complex compounds, including cephalosporins, penicillins, carbapenems, and aminoglycosides. This versatile reagent can be used to synthesize a wide variety of organic compounds.

Please enquire for more information about 4-Ethyl-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications Methyl 2-(1-(5-Fluoropentyl)-1H-indole-3-carboxamido)-3-phenylpropanoate is a useful intermediate for organic synthesis. It is a derivative of I-AMB (I110000(M)), which is an analog of 5-fluoro AMB that was developed on an indole base instead of the indazole base typically associated with AB-PINACA. References Shevyrin, V., et al.: Chem. Heterocyclic Comp., 50, 583 (2014)

6-Bromo-1-chloroisoquinoline is a chemical compound that belongs to the group of disulfides. It is an optical isomer of 6-bromo-1-chloroisoquinoline, which is used as a starting material for the synthesis of other compounds. The synthesis of 6-bromo-1-chloroisoquinoline from acetonitrile and phosphorus oxychloride can be achieved using a Grignard reagent with an xanthate and halides. This reaction produces alkyl chlorides, which can be converted in turn into sulfones or sulfoxides. This compound has been shown to react with sodium sulfide and carbon disulphide to form the corresponding disulfide. 6-Bromo-1-chloroisoquinoline has also been shown to react with phosphine and sulfide to form polysulphides.

Please enquire for more information about 2-(5-Chlorothien-2-yl)-6,8-dimethylquinoline-4-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-(4-Methylphenoxy)quinoline-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 9-(2’-O-Acetyl-5’-O-benzoyl-3’-O-methyl-beta-D-ribofuranosyl)-6-chloropurine including the price, delivery time and more detailed product information at the technical inquiry form on this page