Ethers

3,5-Dimethoxybenzhydrazide is a combretastatin analogue that binds to tubulin to disrupt the polymerization of microtubules. It has been shown to inhibit tumor cell growth in vitro and in vivo. 3,5-Dimethoxybenzhydrazide has an IC50 of 10 nM for tubulin polymerization, which is significantly lower than colchicine (IC50 of 0.2 μM). This drug also interacts with colchicine binding sites and has a selectivity index of 1.3.

Produces fluorescent benzimidazole derivatives; detects aromatic aldehydes

2,2'-Dimethoxybiphenyl is a thermoplastic that is exothermic, making it useful in the production of polyketones. It can be used as a linker to form covalent bonds with monomers and polymers. 2,2'-Dimethoxybiphenyl has been used as a monomer to produce polyethers and polyesters. This compound has many chemical stability properties, which makes it suitable for use in polymer synthesis. It also can react with nucleophiles such as amines to form ether linkages. 2,2'-Dimethoxybiphenyl has kinetic properties that are faster than those of other ketones but slower than those of other ether-linked compounds. The activation energy for its reaction is low, making it an effective monomer for polymerization reactions.

2-Ethoxybenzonitrile is a non-natural molecule that is synthesized from the reaction of aniline and ethyl bromide. The reactants are heated together in the presence of an acid catalyst to form 2-ethoxybenzonitrile. 2-Ethoxybenzonitrile has been used as a research chemical in pharmaceutical research because it can be substituted for other molecules, such as benzene or nitro compounds, with similar physical properties. This synthetic compound has been shown to have a constant boiling point and melting point, which is desirable for use in molecular modeling studies. The molecule also has two isosteres that can be used in its place: dimethoxybenzene and diphenyl ether. 2-Ethoxybenzonitrile has been shown to react with purines by forming a C(2)-N bond. These reactions are catalyzed by nitro compounds, which act as electron donors. The mechanism of these reactions is

Please enquire for more information about 2-Chloromethyl-3-methyl-4-(2,2,2-trifluoroethoxy)pyridine, hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

1-Ethoxy-2-methoxybenzene is an organic compound that belongs to the class of phenols. It has been used as a solvent for pharmaceutical formulations, as an extractant for human serum, and as a demethylating agent in analytical chemistry. 1-Ethoxy-2-methoxybenzene is used in the presence of hydrochloric acid and morpholine to produce dibutyl ether from diethyl ether. This reaction is catalyzed by chloride ions, which are present at high concentrations in the solution. The linear response of this analytical method can be attributed to its acidic properties. The use of microwaves during this reaction allows for increased chemical yields and decreased time needed for the reaction to occur.

Please enquire for more information about (3-(2,6-dichlorophenyl)-5-methylisoxazol-4-yl)-N-(2,5-dimethoxyphenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

Diethyl ethoxymethylidenemalonate is a matrix effect reagent used in analytical chemistry. It is often used as a substrate for the cycloaddition process, which produces malondialdehyde and hydrochloric acid. The UV-absorption of the malondialdehyde can be measured to determine the concentration of the sample. Diethyl ethoxymethylidenemalonate is also used as a dna template in binding constants, where it binds with amines to form complexes that are then analyzed by light emission. It has been shown to have an inhibitory effect on gyrase and trifluoroacetic acid, both enzymes involved in DNA replication.

4-Methoxybenzaldehyde is a surfactant with a Langmuir adsorption isotherm. It can be used in analytical methods for the determination of sodium carbonate at concentrations of 1 mg/mL and higher. The redox potentials of 4-methoxybenzaldehyde are +0.37 and -0.35 volts, which corresponds to group P2. The reaction mechanism for 4-methoxybenzaldehyde is the oxidation of the compound by potassium permanganate (KMnO4) in aqueous solution to form 4-hydroxybenzoic acid (4HB). The fluorescent derivative of 4-methoxybenzaldehyde is magnesium salt, which has been shown to react with ryanodine receptors in skeletal muscle cells, leading to a decrease in calcium release from the sarcoplasmic reticulum. Process optimization may be necessary for this product due to its limited applications in analytical chemistry.

2,4,6-Tribromo-3-methoxyphenol is a high quality reagent that is used as an intermediate in the production of many fine chemicals. It is also a useful building block for the synthesis of speciality chemicals and research chemicals. This chemical can be used as a versatile building block for reactions with other compounds. 2,4,6-Tribromo-3-methoxyphenol has CAS number 24967-79-1 and can be found at Chemical & Laboratory Equipment.

4-Methoxybenzoic anhydride is a nonsteroidal anti-inflammatory drug (NSAID) that has a hydroxy group, which makes it susceptible to nucleophilic attack. The reaction mechanism of 4-methoxybenzoic anhydride involves hydroxyl group and phosphorus pentachloride. Kinetic data for the reaction was obtained from kinetic studies. The kinetic study found that the rate of the reaction increased with increasing concentration of amines and amides in the reaction mixture. 4-Methoxybenzoic anhydride has been shown to have antiinflammatory activity in various tests on animals, including rats, guinea pigs, and rabbits. The mechanism of this activity may be due to its ability to inhibit prostaglandin synthesis by blocking cyclooxygenase enzyme activity.

4-Hydroxy-3,5-dimethoxybenzamide is a phenolic compound that is soluble in organic solvents. It has been shown to bind to fatty acid sequences and neutral polypeptides in the presence of an acidic or basic environment. 4-Hydroxy-3,5-dimethoxybenzamide has also been shown to have catalytic activity, which may be due to its ability to form a polymeric matrix with other compounds.

5-Methoxyresorcinol is a plant product that has been shown to inhibit protein synthesis. It was found to have a second-order rate constant of 0.079 M-1s-1 at pH 7, which is much lower than the first order rate constant for urea hydrolysis (0.71 M-1s-1). 5-Methoxyresorcinol has also been shown to demethylate methyl glycosides and synthesize cell cultures. This product inhibits the replication of herpes simplex virus by inhibiting the synthesis of viral proteins in infected cells and blocking the maturation of progeny virus particles.

[4-(2-Aminoethoxy)phenyl](phenyl)methanone HCl is a fine chemical that belongs to the group of versatile building blocks. It can be used as a reagent, speciality chemical, useful building block, high quality research chemical, or useful intermediate. The CAS registry number is 1185504-45-3.

Please enquire for more information about (2-(3,4-dimethoxyphenyl)ethyl)(phenylsulfonyl)amine including the price, delivery time and more detailed product information at the technical inquiry form on this page