Alcoli

Quinoline-5-carboxylic acid is a peroxide that is produced by the oxidation of quinoline derivatives. Quinoline-5-carboxylic acid has been shown to have antibacterial activity, and it also has affinity values for chloride ions. The chemical isomers of quinoline-5-carboxylic acid are called quninolines, which are produced by the hydrolysis of quinoline-5-carboxylic acid. Quinolines can be obtained by the oxidation of aniline. Quinolines have been shown to catalyze reactions with carbonyl groups in organic molecules, such as the reaction between an alkoxycarbonyl group and a hydroxyl group to form an aldehyde or ketone. Kinetic data for this reaction was obtained using titration calorimetry.

2-Bromo-4-methylphenol is an organic compound that has interactive effects with hydrochloric acid, molybdenum, and trifluoromethanesulfonic acid. It is soluble in water vapor, but insoluble in polyvinyl. 2-Bromo-4-methylphenol reacts with sodium hydroxide solution to form a hydroxide solution and sodium carbonate. The reaction product of 2-bromo-4-methylphenol with triterpenoid saponin produces fatty acids. This reaction occurs because the hydroxide ion from the sodium hydroxide solution attacks the ester group of the saponin, forming an alcohol group on one end and a carboxylic acid group on the other end. The benzyl groups are removed by hydrogenation to produce phenol.

Ethyl-2-aminoquinoline-3-carboxylate is an intramolecular reductive coupling product. It was synthesized by the reductive coupling of nitrobenzene with triethylamine in the presence of a copper salt. The use of ethyl cyanoacetate as a starting material for this synthesis has been shown to produce regioselective products with high yields. Ethyl-2-aminoquinoline-3-carboxylate is used in the synthesis of quinoline derivatives and fluoroquinolone antibiotics. This compound has been shown to have optimum properties for GC/MS analysis, which makes it an advance in the field of chemistry.

Deoxynivalenol is a mycotoxin that is produced by the fungi Fusarium graminearum and F. culmorum. It produces toxic effects in humans and animals, including human immunoglobulin E (IgE) production, acute toxicities, and cytotoxic effects on cultured human leukocytes. The analytical method for deoxynivalenol detection includes a variety of in vitro methods such as enzyme-linked immunosorbent assays (ELISA), competitive ELISA, fluorescent antibody staining assay, fluorescence polarization immunoassay (FPIA), competitive FPIA, and high performance liquid chromatography (HPLC). Deoxynivalenol binds to dna with high affinity and has been shown to have fusarial activity. The toxicity of deoxynivalenol can be confirmed by the mitochondrial membrane potential assay or by the assessment of vomitoxin levels. Colloidal gold can be used for identification of deox

Quinoline-2,8-diol is a bacterial strain that can be used to remove fatty acids from wastewater. The recombinant cytochrome P450 in this strain can degrade fatty acids, which are carcinogenic and have been shown to cause hepatic steatosis. In addition, the quinoline-2,8-diol strain has shown an ability to inhibit xenograft tumor growth in mice by activating cytochrome P450 and inducing apoptosis. This bacterial strain also has the potential to produce xanthurenic acid from tyrosine. Xanthurenic acid is toxic and has been shown to inhibit polymerase chain reaction (PCR) amplification of DNA. Quinoline-2,8-diol may be used as a model for experimental studies of xanthurenic acid's effects on energy metabolism and DNA synthesis.

Please enquire for more information about 4-(2-methyl(8-quinolyloxy))-1-nitrobenzene 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-(4-Bromophenyl)-5-(hydroxyimino)-7,7-dimethyl-6,7,8-trihydrocinnoline including the price, delivery time and more detailed product information at the technical inquiry form on this page

16alpha,17alpha-Epoxypregnenolone is a synthetic insect odorant that binds to the odorant binding protein (OBP) and has been used in research to investigate the relationship between odorant binding and olfaction. The OBPs are thought to play an important role in the detection of odors by binding to specific odorants, which then initiate a sensory response. 16alpha,17alpha-Epoxypregnenolone has also been shown to bind with recombinant OBP and have fluorescence properties, making it useful for biosensors. This compound may be useful as an experimental or research tool for investigating olfactory receptors in insects or other organisms.

Please enquire for more information about 2-Indol-3-yl-2-oxo-N-(8-quinolyl)ethanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 1,3-Dihydro-1-hydroxy-2,1-benzoxaborol-5-ol is used as a reagent in the synthesis of P4-benzoxaborole-substituted macrocyclic inhibitors of HCV NS3 protease.
References Ding, C.Z., et al.: Bioorg. Med. Chem. Lett., 20, 7317 (2010)

Applications 4-Hexadecyloxyphenol is used as a reactant in the enzyme-mediated two-dimensional polymerization of aromatic derivatives on a Langmuir Trough.
References Bruno, F., et al.: Ind. Eng. Chem. Res., 34, 4009 (1995)

Applications Cyclopentaneethanol is used in the prepartion of phenylalanine derivatives for incorporation into peptides as CD4 mimetic miniproteins interacting with HIV-1 surface glycoprotein. It is also used in the preparation of tertiary amine muscarinic receptor antagonists applied towards the treatment of chronic obstructive pulmonary disease.
References Morellato-Castillo, L. et al.: J. Med. Chem., 56, 5033 (2013); Glossop, P. et al.: J. Med. Chem., 54, 6888 (2011);

Applications 1-(9H-Purin-6-ylamino)propan-2-ol is a reagent used for organic synthesis and also functions as a plant growth regulator.
References Gao, Y., et al.: J. Heterocyclic Chem., 53, 579 (2016); Oda, A., et al.: From Faming Zhuanli Shenqing (2016), CN 105503875 A 20160420; Lira, E. P.: J. Org. Chem., 33, 3355 (1968)

Applications 3-Phenyl-1-butanol is a reactant with primary alcohol functional group which is oxidized to aldehyde using the nanoparticle-ferrite-palladium catalyst.
References Polshettiwar, V., Varma, R.: Org. Biomol. Chem., 7, 37 (2009);

Applications 2-Tributyltin-allyl-1-ol (cas# 84666-30-8) is a compound useful in organic synthesis.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

Applications 3,4-Diaminophenol (cas# 615-72-5) is a useful research chemical.