Éthers

Applications 1,1-Dimethoxycyclohexane (cas# 933-40-4) is a useful research chemical.

Applications 7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one is a substituted benzazepinonee derivative used in the preparation of bradycardic agents as well as isoform-selective f-current blockers.
References Liang, H.-Y. et al.: Arch. Pharm., 343, 114 (2010); Reiffen, M. et al.: J. Med. Chem., 33, 1496 (1990); Melchiorre, M. et al.: J. Med. Chem., 53, 6773 (2010);

Stability Store at -20°C under Argon. Air Sensitive.
Applications 5,5-Diethoxypentanal (cas# 79893-96-2) is a compound useful in organic synthesis.

Applications Ethoxybenzene is a reagent used in the synthesis of benzenesulphonylurea derivatives as anti-hyperglycaemic agents and various PTP1B inhibitors.
References Liu, P. et al.: Bioorg. Med. Chem., 23, 7079 (2015);

Applications Methyl Methoxyacetate is a reagent used in the synthesis of diphenylamine-terepthalaldehyde resins which maybe be used as a catalyst for tetrahydropyranylation.
References Tanemura, K. et al.: Org. Prep. Proc. Int., 48, 72 (2016); By: Robiette, R. et al.: J. Am. Chem. Soc., 138, 737 (2016);

Impurity Lubiprostone Impurity VI
Applications 7-((1R,2R,3R)-3-(cyclohexylmethoxy)-2-(4,4-difluoro-3-oxooctyl)-5-oxocyclopentyl)heptanoic Acid is a useful chemical reagent.

Stability Light Sensitive
Applications Cis-1-Bromo-2-ethoxyethylene

Applications 1-[3,4-Bis(phenylmethoxy)phenyl]ethanone is an intermediate in synthesizing Arbutamine (A766300). It is a cardiac stimulant. Arbutamine stimulates adrenergic receptors.
References Sinusas, A., et al.: J. Nucl. Med., 35, 664 (1994); Sansoy, V., et al.: Circulation, 92, 994 (1995); Elhendy, A., et al.: Eur. J. Nucl. Med., 23, 1354 (1996);

Stability Hygroscopic
Applications Ethyl 3,3-diethoxypropionate

Applications (2R,​3S,​4S,​5S)-5-Hydroxy-2,3,4-tris(phenylmethoxy)-5-[(phenylmethoxy)methyl]-cyclohexanone was used in the synthetic preparation of N-substituted valiolamine derivatives.
References Fukase, H., et al.: J. Org. Chem., 57, 3642 (1992);

Applications 4,4'-Dimethoxybenzhydrol acts as a reagent in the preparation of aryloxyacetamide derivatives and their biological activity as neuroprotective agents. Preparation and anticancer activity of quebecol and analogs.
References Zhong, Y., et al.: Bioorg. Med. Chem. Lett., 26, 2526 (2016); Pericherla, K., et al.: Bioorg. Med. Chem. Lett., 23, 5329 (2013)

Applications Reagent used in Phthalimidooxy alylation.
References Yoda, R., et al.: Chem. Pharm. Bull., 42, 686 (1994), Kim, M., et al.: Bioorg. Med. Chem. Lett., 6, 2077 (1996),

Applications 3,3-Diethoxy-1-propanol is used as a reactant in the synthesis of nanoparticles.
References Sumitani, Shogo, et al.: Reactive & Func. Polymers, 71(7), 684-693 (2011);Kanakubo, Yurie, et al.: Colloids and Surfaces, B, 78(1), 85-91 (2010)

Stability Hygroscopic

Applications 2-[2-(2-Propynyloxy)ethoxy]ethanol is a reactant used in the preparation of divalent ligands based on 3-deoxy-4-thiolactose as inhibitors of E. coli β-galactosidase.
References Cagnoni, A.J., et. al.: Org. Biomol. Chem., 11, 5500 (2013)

Applications 1,2,3-Trimethoxybenzene can be used for RSM-optimised slow pyrolysis of rice husk for bio-oil production.
References Das, S., et.al.: Energy, 225, 120161, (2021);

Applications Methyl 2-Acetyl-4,4-dimethoxybutanoate is a useful reagent for organic synthesis.
References Herrmann, J. L., et al.: Tetrahedron Lett., 47, 4711 (1973)

Applications Tetramethoxypropane is a useful synthetic intermediate. It can be used to synthesize various compounds such as diiodonoradamantane and Salicylates[e.g. Salsalate(S095700)].
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Ioannou, S., et al.: Tetrahedron Lett., 51, 2671 (2010); Sher, M., et al.: J. Org. Chem., 72, 6284 (2007)

Applications Methyl Dimethoxyacetate is used as a reagent in the synthesis of benzimidazole derivatives for use as respiratory syncytial virus inhibitors.
References Cooymans, Ludwig Paul; D., et al. PCT Int. Appl. WO 2012080446 A1 20120621. Jun 21, 2012

Applications Repaglinide intermediate.
References Wolfenbuttel, B., et al.: Eur. J. Clin. Pharmacol., 45, 113 (1993), Grell, W., et al.: J. Med. Chem., 41, 5219 (1998), Anon., et al.: Drugs Future, 24, 815 (1999),

Applications Synthesis and receptor binding of 5-(amino[3H]2methyl)-3-isothiazolol ([3H]thiomuscimol), a specific GABAA agonist photoaffinity label.
References Frolund, B., et al.: J. Labelled Compounds Radiopharm., 36, 877 (1995),

Applications 5-[2-(Trifluoromethoxy)phenyl]-2-furancarboxylic Acid is a reactant used in the preparation of (phenyl)-N-[(mercapto)(pyrrolyl)triazolyl]furancarboxamide and (phenoxy)-N-[(mercapto)(pyrrolyl)triazolyl]acetamide derivatives as herbicides.
References Xue, S., Lu, C.: Youji Huaxue, 28, 1083 (2008)

Stability Moisture Sensitive
Applications (3R,4R)-Dihydro-3,4-bis(phenylmethoxy)-2,5-furandione is an intermediate in the synthesis of N-alkenylsuccinimide derivatives.
References Ohwada, J., et al.: Bull. Chem. Soc. Jap., 63, 287 (1990);

Stability Light and Temperature sensitive
Applications PFPA-silane is a functionalized perfluorophenyl azides for covalent immobilization of ultrathin polymer films.
References Mosbach, K., et al.: Biotechnology, 14, 163 (1996), Keren, K., et al.: Science, 297, 72 (2002), Lidstrom, M., et al.: Nature Rev. Microbiol., 1, 158 (2003),

Applications N-[[4-(Phenylmethoxy)phenyl]methyl]-2-[(3-thienylcarbonyl)amino]-4-thiazoleacetamide is derived from ethyl 2-amino-4-thiaxolacetate (E899330) which is used in the synthesis of various pharmaceutical and biologically active compounds including inhibitors and antibiotics.
References Inamoto, Y., et al.: J. Antibiot., 41, 828 (1988)

Applications 4,5-Dimethoxy-1-benzocyclobutenecarbonitrile is used in the preparation of selective bradycardic agents.
References Ye, X. et al.: Zhong. Yao. Xuax. Zaz., 20, 106 (2010);

Applications 2-(1,1-Dimethylethoxy)-1-propanol is a useful reagent for organic synthesis.

Applications Methyl 4-(trifluoromethoxy)benzoate

3-(4-Methoxyphenyl)pyrazole is a fungicide that belongs to the group of nitrophenol derivatives. It inhibits the growth of plant pathogenic fungi by inhibiting the synthesis of proteins and nucleic acids. 3-(4-Methoxyphenyl)pyrazole has an inhibitory effect on seed germination and germination, as well as on hydroxymethylation reactions in fungal mycelia. 3-(4-Methoxyphenyl)pyrazole also has bactericidal properties and can be used for controlling bacteria in water systems.

2-(2-Methoxyphenoxy)ethylamine base is an inorganic base with a hydroxyl group. It is soluble in organic solvents and has been used as a coumarin derivative. 2-(2-Methoxyphenoxy)ethylamine base has shown potential use as an antifungal agent, which may be due to its ability to cause lysis in fungi cells. This compound has also shown in vitro activity against bacteria and viruses, including herpes simplex virus type 1 and HIV-1. The 2-(2-methoxyphenoxy)ethylamine base can be sulfonated or acid catalyzed to produce other derivatives that have potential use as anti-inflammatory or analgesic agents.

4-(Trifluoromethoxy)phenylboronic acid is a boron-containing compound that has been shown to be a potent inhibitor of the histone deacetylase (HDAC) enzyme. It also has surfactant properties and can be used as a photochemical reagent. 4-(Trifluoromethoxy)phenylboronic acid is orally bioavailable and may have therapeutic potential for neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, and Huntington's disease. It also has the ability to inhibit cancer cell growth by inhibiting HDAC activity. This drug has been found to cross-couple with organosilicon compounds in order to form new compounds with potent inhibitory activity against HDAC enzymes.

4-Chloro-2,5-dimethoxynitrobenzene (CDMNB) is a solvent and a synthetic intermediate. It is soluble in diethylene, solvents, and sodium formate. CDMNB can be reduced with catalytic reduction or amines to 2,5-dimethoxybenzoic acid. CDMNB has been shown to react with xylene under catalytic conditions to produce 4-chloro-3,5-dimethoxybenzoic acid. This reaction can be monitored by liquid phase chromatography or cyclic voltammetry.

4-Hydroxy-7-methoxyquinoline is an anti-malarial drug that belongs to the class of trimethyl, trifluoromethyl group. It is a cyclic compound and its synthesis starts with cyclization of the methyl derivative, which forms a ring. This product is used in clinical practice as an inhibitor of malarial protozoa and has been shown to have mechanistic effects on the cytochrome bc1 complex containing red blood cells. 4-Hydroxy-7-methoxyquinoline also inhibits the growth of bacteria by binding to the enzyme methionine synthase, which is involved in the biosynthesis of methionine from homocysteine. The product also has an inhibitory effect on DNA synthesis and protein synthesis.

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Methyl trans-3-methoxy acrylate is a reactive monocarboxylic acid. It is used in the synthesis of other compounds, such as polymers and pharmaceuticals. Methyl trans-3-methoxy acrylate reacts with hydrogen chloride to form methyl 3-chloroacrylate and hydrochloric acid, and with trimethyl borate to form methyl 3-bromoacrylate. The reaction mechanism for the formation of methyl 3-bromoacrylate is similar to that for the formation of methyl 3-chloroacrylate. The reaction can be carried out in a steel or glass vessel equipped with a magnetic stirring device and equipped with an electric heating mantle or flame. The activation energies for these reactions are relatively high at 43 kcal/mol (for the metathesis reaction) and 44 kcal/mol (for the reaction with trimethyl borate). This product has been shown to react with propionate