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Please enquire for more information about 2-(4-Ethylphenyl)-6-methylquinoline-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 1-Phenyl-3-(quinolin-8-ylamino)propan-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 7-Bromoquinolin-2(1H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 1H-Indazole-3-carboxylic acid, 6-[(dimethylamino)methylene]-4,5,6,7-tetrahydro-1,4,4-trimethyl-7-oxo-,ethyl 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-(Quinolin-7-yl)acetic 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 2,3-Dihydro-1H-cyclopenta[b]quinoline-9-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Chloroquinoline is a chemical compound that has been analysed using spectroscopy. It has been shown to have cross-coupling reactions with a number of organic compounds. 5-Chloroquinoline can be synthesized from 1,2,4-triazole and chloroacetyl chloride in the presence of an acid catalyst. This synthesis requires the use of dry solvents to remove moisture and prevent hydrolysis. 5-Chloroquinoline can also be synthesized by reacting phenol with 2,4,6-trichlorophenol and then adding sodium hypochlorite in ethanol to produce the desired product. The magnetic properties of 5-chloroquine have also been studied using nuclear magnetic resonance (NMR) studies and it has been found that this compound is capable of undergoing proton exchange without any change in its chemical structure. The theory behind these reactions is still being researched.

Please enquire for more information about 2-(2-Chlorophenyl)-6-ethylquinoline-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 9-(3-Deoxy-3-fluoro-beta-D-ribofuranosyl)-6-phenylpurine including the price, delivery time and more detailed product information at the technical inquiry form on this page

8-Hydroxyisoquinoline is a heterocyclic compound that is synthesized from the reaction of acetylacetone with hydroxylated isoquinoline. It has two stereoisomers and four possible alkyl substituents. 8-Hydroxyisoquinoline can be used as a reagent for the synthesis of other compounds, such as sulfoxides, which are intermediates in organic reactions. The reaction can be carried out at room temperature and the product will precipitate from the solution due to its high solubility in water. This process is not very efficient, so it is best to use a large amount of solvent and increase the reaction time to obtain higher yields. The purity of this compound can be determined by using gel chromatography and anhydrous sodium acetate. 8-Hydroxyisoquinoline's skeleton contains a ligand group that binds to metal ions, which makes it useful for hypotensive drugs.

Please enquire for more information about 2-(4-sec-Butylphenyl)-8-chloroquinoline-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-(Pinacolateboryl)indole including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Amino-6-bromopurine is a cancer drug that is currently undergoing clinical trials for the treatment of prostate cancer. This drug has shown to be effective in treating prostate cancer cells that are resistant to castration, which are not sensitive to this hormone. 2-Amino-6-bromopurine inhibits DNA polymerase, leading to apoptosis in prostate cancer cells. It also interacts with the thiopurine S-methyltransferase enzyme, which leads to the production of 6-mercaptopurine and 6-thioguanine, which can block DNA synthesis by inhibiting ribonucleotide reductase and thymidylate synthase. 2-Amino-6-bromopurine has been shown to inhibit mutations associated with metastatic castration resistant prostate cancer.

6-Amino-2-iodopurine is a purine derivative that is used to study hypoxanthines. It can be converted to 2-chloroadenine, which has been shown to cause damage to cells in tissue culture. 6-Amino-2-iodopurine has also been shown to cause sarcomatous transformation of skin cells and the formation of 2-chloroadenosine and 2-aminoadenosine. These compounds are toxic and have been found in damaged DNA. 6-Amino-2-iodopurine also has substituents on the purines, which are damaged when they react with DNA.

6-Fluoro-2-quinolinecarbaldehyde is a ligand that binds to the axial position of the heme group of galactose oxidase. It is used in biochemistry as an oxidant for studies on the chemistry of sugar synthesis and degradation. 6-Fluoro-2-quinolinecarbaldehyde is a phenol with three carbonyl groups, and it can be protonated to form a tripodal ion. The molecule has been shown to act as an oxidant in galactose oxidation reactions. The compound is also able to bind to the enzyme's heme group and inhibit catalysis by competing with oxygen for binding sites on the heme iron atom.