Éthers

Please enquire for more information about 3-Methoxy-2-naphthohydrazide including the price, delivery time and more detailed product information at the technical inquiry form on this page

6-Methoxy-1,3-benzodioxole-5-carbaldehyde is a diastereomer of the compound phrymarolin. This chemical has been shown to have an aldol condensation reaction with carbonate and methylamine to form sesamol, which is a precursor to the drug piperidide. 6-Methoxy-1,3-benzodioxole-5-carbaldehyde is also used in the synthesis of cadmium compounds, including cadmium salts and cadmium oxide.

N-Hydroxy-3-methoxy-benzamidine is a versatile compound that finds applications in various fields, including research chemicals and cosmeceuticals. It is derived from Huperzia serrata, a plant known for its medicinal properties. N-Hydroxy-3-methoxy-benzamidine has been extensively studied for its potential as an electrode material due to its unique vibronic coupling properties. In addition, it has shown promising results in regulating progesterone concentration, making it a valuable tool in hormonal studies. This compound belongs to the heterocycle family and can be easily derivatized into different forms, such as seven-membered benzoate derivatives. Studies have also indicated that N-Hydroxy-3-methoxy-benzamidine can affect plasma progesterone concentrations and interact with ginsenosides. Furthermore, it exhibits interesting emission properties when combined with n-acyl or estradiol benzoate compounds. Its multifaceted characteristics

Please enquire for more information about 6-(1-Bromoethyl)-N-(2-methoxyphenyl)-1,3,5-triazine-2,4-diamine 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-Methyl-3-(3-methoxypropoxyl)benzoicacid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about N-(4-methoxyphenyl)-N'-benzylethane-1,2-diamide 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-Bromo-5-methoxy-4-propoxybenzoyl 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 (R)-2-Methoxypropan-1-amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Hydroxy-3-methoxy-5-nitrobenzoic acid is a monomer that can be used to create polymers. It is an important chemical in the production of vanillin, which is used as a flavoring agent for food and drink. Vanillin is also used in perfumes, as well as for treating leather and wood. Demethylation of 4-hydroxy-3-methoxy-5-nitrobenzoic acid results in the formation of cinnamic acid, which can be converted into cinnamic alcohol or cinnamic acid derivatives. The conversion of 4-hydoxy-3-methoxy-5 nitrobenzoic acid to cinnamic acid derivatives may be catalyzed by metals such as nickel or palladium. The recycling process can be optimized by changing the temperature and magnetic field strength during the reaction process.

Please enquire for more information about 1-(2,3,4-Trimethoxyphenyl)octahydroisoquinolin-4a(2H)-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page

1-(4-Methoxyphenyl)-N-(naphthalen-1-ylmethyl)methanamine,hydrochloride (MTL) is a drug that belongs to the group of drugs used in cancer therapy. It is an inhibitor of the p38 mitogen-activated protein kinase (MAPK), which has been shown to play an important role in the development and progression of cancer. MTL has also been shown to inhibit intracellular glutathione, which is essential for scavenging reactive oxygen species and maintaining cellular redox balance. MTL can be used as a treatment for neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease, as well as traumatic brain injury. This drug also has a viscosity that minimizes blood flow loss from wounds and other injuries.

Please enquire for more information about 1-(3-Methoxypropyl)-2,5-dimethyl-1H-pyrrole-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Ethyl chloro(ethoxy)acetate is a cycloaddition product of ethyl chloroacetate and an aldehyde or ketone. It can be synthesized by the Wittig reaction, which involves the reaction of an alkyl phosphonium salt with an aldehyde or ketone. Ethyl chloro(ethoxy)acetate undergoes thermolysis to form a dipole and imine, which then reacts with hydroxylamine to generate phosphonium ylide. The ylide then reacts with another molecule of ethyl chloro(ethoxy)acetate to form the desired cycloadduct. This chemical has been shown to have potential as a research tool in organic synthesis.

Please enquire for more information about (5E)-5-(4-Ethoxybenzylidene)-2-mercapto-3-phenyl-3,5-dihydro-4H-imidazol-4-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

The structure of the molecule is a furan, oxadiazoles, dihydro, benzamide, dibasic, disubstituted, dihedral. The molecule has an unwanted nematicidal activity. The molecule is hydrogen bonded to the benzene. The molecule also inhibits nematodes.

Please enquire for more information about 3-Ethoxy-2-Fluorophenylboronic Acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

8-Methoxyisoquinoline is a synthetic compound and is used in the manufacture of pharmaceuticals. It is also used to produce insecticides, herbicides, and fungicides. 8-Methoxyisoquinoline has been shown to be effective against infectious diseases such as malaria and leishmaniasis. This compound can be found in natural products such as protoberberine alkaloids and has been shown to inhibit acetylcholinesterase (AChE) activity. It has also been shown to inhibit the growth of bacteria that are resistant to erythromycin, tetracycline, chloramphenicol, and penicillin.

3-Chloro-4-methoxy-benzylamine is a quinoline derivative that is used in the synthesis of pharmaceuticals. It is a chlorinating agent that forms a hydrogen bond with other molecules to produce an alkylated product. 3-Chloro-4-methoxy-benzylamine has been shown to inhibit the activity of cyclic guanosine monophosphate (cGMP) and phosphodiesterase type 5 (PDE5). This inhibition leads to an anti-obesity effect in mice by promoting weight loss. 3CMB also inhibits the production of amyloid beta peptide and prevents Alzheimer's disease, as well as inhibits seizures caused by epilepsy.

Please enquire for more information about 2-(3-Methoxyphenyl)-8-methylimidazo[1,2-a]pyridine-3-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,6-Dimethoxytoluene is a regiospecific pentafluorophenyl compound with a thermal isomerization. It is an extractive yield that can be isolated from the reaction of acetaldehyde and formaldehyde in the presence of an imine. The process of making 2,6-dimethoxytoluene begins by reacting chloromethane with oxygenated tetrafluorobenzyne to make an intermediate. Then, this intermediate reacts with methoxylated fatty acids to create the final product. This reaction is stereoselective because it produces only one stereoisomer of 2,6-dimethoxytoluene.

2-Methoxyphenylboronic acid is a boron compound that can react with organic compounds to form new carbon-carbon bonds. It is used in biological systems as an enzyme inhibitor and has been shown to be specific for epidermal growth factor receptor. 2-Methoxyphenylboronic acid binds to the active site of epidermal growth factor (EGF) receptor, which prevents the activation of the EGF signaling pathway. This inhibition results in decreased proliferation of epidermal cells and leads to the inhibition of cell growth. 2-Methoxyphenylboronic acid also inhibits the production of proton by binding to ATPase, which may result in a decrease in ATP synthesis and cell death.

3-Bromo-5-methoxyphenylboronic acid is a hydrophobic organic molecule. It can be used in the synthesis of fluorescent dyes and other molecules with hydrophobic properties. 3-Bromo-5-methoxyphenylboronic acid is a small molecule that has a diameter of 1.7 nm and an energy transfer distance of 2.8 nm, which are both less than the typical energy transfer distances for aromatic systems. It is soluble in many solvents, such as water or methanol, but not in others, such as hexane or acetone. This compound has been shown to form dimers when dissolved in water at a concentration greater than 0.1 M and under conditions where the pH is greater than 8.br>br> 3-Bromo-5-methoxyphenylboronic acid has been synthesized by reacting phenyl boronic acid with 3-