Ethers

<p>1-(2-Methoxyphenyl)piperazine is a drug that has been shown to have locomotor activity, antihypertensive activity, and inhibitory properties. It also acts as a matrix effect and receptor activity. 1-(2-Methoxyphenyl)piperazine has been shown to have inhibitory effects on 5-ht7 receptors, which are mainly found in the brain. This drug binds to the 5-ht2 receptor, which is a type of serotonin receptor in the brain. The binding of 1-(2-methoxyphenyl)piperazine to the 5-ht2 receptor inhibits the release of dopamine from neurons and leads to necrotic cell death. This drug can also be used as an analytical tool for measuring 5-ht1a receptors, which is a type of serotonin receptor found in the brain.</p>

<p>Please enquire for more information about 1-(3-Methoxyphenyl)piperazine dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 1-(2-Methoxyethyl)-1H-indole-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(S)-(-)-2-Hydroxy-4-(2-methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide is a crystallization inhibitor. It can be used in the treatment of osteoporosis and to prevent the calcification of prostate tissue. (S)-(-)-2-Hydroxy-4-(2-methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide has been shown to inhibit nucleation and crystal growth by adsorbing to the surfaces of nuclei and inhibiting inhibitor molecules from diffusing into the nucleus. This compound also inhibits the crystallization process by binding to one molecule of phosphate on each phosphate site on a crystal surface. The result is that there are fewer sites available for other molecules to bind, preventing crystal growth.</p>

<p>Please enquire for more information about 1-(Chloroacetyl)-4-(4-methoxyphenyl)piperazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 1-(2,4-Dimethoxyphenyl)piperazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methoxypropoxypropanol (MPP) is a highly selective inhibitor of the enzyme picolinic acid carboxylase, which converts L-pyridoxal 5'-phosphate to picolinic acid. MPP has shown good efficacy in reducing disease activity in animal models and is being developed for the treatment of rheumatoid arthritis. This drug also has been shown to be toxicologically safe in both acute and chronic toxicity studies. Methoxypropoxypropanol has also been used as an analytical reagent for the qualitative detection of picolinic acid in urine and blood samples. The use of this compound as a wastewater treatment agent for removal of organic acids from industrial effluents is well studied. MPP has been found to have some beneficial effects on congestive heart failure in rats by lowering their blood pressure and cholesterol levels.</p>

<p>Please enquire for more information about 1-(2-Ethoxybenzyl)piperazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Chloro-2-(trifluoromethoxy)aniline is a fine chemical that is used as a building block in the synthesis of other chemicals, such as pharmaceuticals and agrochemicals. It is also used in research as a reagent for organic synthesis and as a speciality chemical. 4-Chloro-2-(trifluoromethoxy)aniline has versatile applications in the manufacture of complex compounds, intermediates, and scaffolds.</p>

<p>2,7-Bis[2-(diethylamino)ethoxy]-9-fluorenone dihydrochloride (2,7-BDFE) is a potent inducer of interferon. It is a natural compound that has been shown to have significant cytotoxicity against murine sarcoma virus and opportunistic fungal infections. 2,7-BDFE has also been shown to induce toll-like receptor 4 (TLR4), which triggers the production of other cytokines and chemokines. 2,7-BDFE has also been found to inhibit the growth of cancer cells in vitro and in vivo. This drug is used as an inhibitor for benzalkonium chloride for the prevention of bacterial contamination on surfaces.</p>

<p>Please enquire for more information about Ethyl 2-(2-chloroethoxy)acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Intermediate in the synthesis of osimertinib (AZD9291)</p>

<p>Please enquire for more information about Methoxycarbonyl-D-Nle-Gly-Arg-pNA acetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Trans-4-Benzyloxy-3-methoxy-beta-nitrostyrene is an oxime that can be used as a catalyst for the catalytic hydrogenation of nitroalkanes. It is also a precursor to pallimamine, which is used as a pharmaceutical agent and an experimental virucide. Trans-4-Benzyloxy-3-methoxy-beta-nitrostyrene is synthesized by coupling two indole carboxylic acid analogues in the presence of sodium hydroxide and potassium carbonate. The reaction yields trans-(4'-benzyloxy)-3'-methoxystyrene, which is then converted to the title compound with ammonium chloride and hydrochloric acid. This compound undergoes acidic hydrolysis to yield the title compound.</p>

<p>5-Bromo-2-(trifluoromethoxy)benzaldehyde is a chemical that is used as a reactant in organic chemistry. It can be used as a building block for the synthesis of complex compounds, or as an intermediate in the preparation of fine chemicals. 5-Bromo-2-(trifluoromethoxy)benzaldehyde is also useful in research and development. It has been used to synthesize pharmaceuticals, pesticides, and other organic compounds.</p>

<p>4-Fluoro-2-methoxyphenol is a fluorinating agent that is used in the manufacture of pharmaceuticals, plastics and pesticides. It has been shown to induce apoptosis in cultured cells by upregulating reactive oxygen species (ROS) and increasing mitochondrial membrane permeability, as well as inhibiting cellular physiology. 4-Fluoro-2-methoxyphenol also inhibits the production of ATP and may be toxic to cells by interfering with dinucleotide phosphate.</p>

<p>Please enquire for more information about 4-Difluoromethoxyphenylboronic acid pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Isobutyl-3-methoxypyrazine is a hydrophobic compound that is not soluble in water. It has a bound form and can be titrated with calorimetry. 2-Isobutyl-3-methoxypyrazine is synthesized by reacting 2,2,4-trimethylpentane with methoxyacetone in the presence of sodium methylate. The compound has been detected as an odorant in numerous plant species and is believed to play a role in plant physiology. 2-Isobutyl-3-methoxypyrazine has been shown to have potent antiviral activity against infectious diseases such as HIV, herpes simplex virus type 1 (HSV1), and varicella zoster virus (VZV). This specific antiviral activity may be due to its ability to bind fatty acids by hydrogen bonds, which may interfere with the synthesis of viral membranes.</p>

<p>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.</p>

<p>5-Amino-2-methoxy-4-methylpyridine is a small molecule that inhibits bromodomains. Bromodomains are protein domains that bind to acetylated lysine residues on histones. 5-Amino-2-methoxy-4-methylpyridine binds to the bromodomain, preventing the acetylated lysine residues from binding with other proteins and inhibiting transcription. This drug has been shown to be effective in treating prostate cancer by interacting with the androgen receptor. 5-Amino-2-methoxy-4-methylpyridine also interacts with ATPase, which may lead to increased levels of ATP production, and has been shown to have antitumor effects in vitro.</p>

<p>Candesartan is a selective angiotensin II receptor antagonist that inhibits the binding of angiotensin II to its receptors, which in turn decreases the activity of angiotensin-converting enzyme. Candesartan cilexetil is an ester prodrug that has been shown to be effective in the treatment of high blood pressure. In the crystalline form, candesartan cilexetil is a white powder with a melting point of 130–135 °C and a solubility in water of &gt;1 g/L. The molecular weight of candesartan cilexetil is 393.8 g/mol and it has a molecular formula C17H21NO2S. The chemical structure consists of two benzimidazole rings coupled together through an ethyl-2-ethoxy linker and attached to a carboxylate group on one end and an amide group on the other</p>

<p>2-(4,5-Dimethoxy-2-(1-((2-methylphenyl)methyl)vinyl)cyclohexyl)ether is a versatile building block for the synthesis of complex compounds. It is also an intermediate in the synthesis of useful scaffolds and reaction components. This compound has a high quality and can be used as a reagent or research chemicals.</p>

<p>Please enquire for more information about 2-Hydroxy-5-methoxybenzimidazole including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-(Difluoromethoxy)-2-mercaptobenzimidazole is an organic solvent that is used in the crystallization process of pantoprazole, a benzimidazole derivative. It is also used as a corrosion inhibitor and pump inhibitor in analytical chemistry. The purity of 5-(difluoromethoxy)-2-mercaptobenzimidazole can be determined by chromatographic methods or by the use of analytical chemistry. Impurities may be genotoxic and include reactive impurities such as thiourea and 2-thiouracil. These impurities are removed during the synthetic process to produce 5-(difluoromethoxy)-2-mercaptobenzimidazole. This drug substance has been found to inhibit DNA polymerase activity in vitro, but its effects on human cells have not been studied.</p>

<p>5-Chloro-2,4-dimethoxyaniline (5-CDA) is a crystalline solid that belongs to the amine class of chemical compounds. It is used in the production of polyhalogenated anilines and nitrosamines, which are known carcinogens. 5-CDA has been shown to be toxic to animals at high doses and can cause health effects such as irritation of the eyes, skin, and respiratory tract; central nervous system depression; and gastrointestinal disturbances. The toxicity of this compound is related to its ability to form nitrosamines when it comes into contact with nitrite or other N-nitroso compounds. 5-CDA is also present in wastewater effluents from paper mills and agricultural runoff from triticum aestivum fields.</p>

<p>Kaempferol-7,4'-dimethoxy-8-butyryl ester is a fine chemical that is used as a versatile building block for the synthesis of complex compounds. It is also used in research chemicals and as a reagent and speciality chemical. Kaempferol-7,4'-dimethoxy-8-butyryl ester has CAS number 1284229-43-1 and can be used as an intermediate for the synthesis of other compounds. It is also a useful scaffold for the synthesis of high quality compounds with potential pharmaceutical applications.</p>

<p>Please enquire for more information about N-(4-Methoxyphenylazoformyl)-Arg-OH·HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>7-Methoxy-4-(trifluoromethyl)coumarin is a potent and selective aromatase inhibitor. It inhibits the activity of the enzyme, which converts testosterone to estradiol. The inhibition of this enzyme may be beneficial in the treatment of breast cancer. This compound has also been shown to inhibit the activity of P450 enzymes and coumarin derivatives, which are involved in drug metabolism and detoxification.</p>

<p>3-Methoxybenzyl chloride is a polymer conjugate that has the chemical formula C6H5CH2ClO. It reacts with hydroxy groups to form ester bonds. The compound was synthesized by reacting 3-methoxybenzyl chloride with hydrochloric acid in vitro, and the resulting product was found to have antimicrobial properties. In vivo studies have shown that this compound binds to receptors in rat striatal tissue. 3-Methoxybenzyl chloride also showed fluorescence properties when exposed to ultraviolet light and can be used for molecular modeling. Titration calorimetry has been used to study the thermal stability of this polymer conjugate.</p>

<p>N-(2-Bromoethoxy)phthalimide is a chemical compound that has been shown to inhibit the activity of histone deacetylases. Histones are proteins that regulate gene expression and play an important role in the regulation of DNA transcription. The enzyme histone deacetylase (HDAC) removes acetyl groups from these proteins, which can lead to changes in gene expression and misregulation of cellular processes. HDACs have been linked to autoimmune diseases, such as arthritis and multiple sclerosis, because they can cause inflammation by affecting the production of inflammatory cytokines. N-(2-Bromoethoxy)phthalimide is able to inhibit HDACs by forming covalent bonds with the lysine residues on these enzymes. This inhibition causes modifications that affect the interaction between HDACs and their substrates, preventing them from modifying histones or interacting with other proteins.</p>

<p>Methyl 3,5-dichloro-4-methoxybenzoate is a fine chemical and useful building block for research chemicals. It belongs to the class of speciality chemicals and can be used as a reagent in organic synthesis. Methyl 3,5-dichloro-4-methoxybenzoate is a versatile building block that has been reported in the synthesis of many complex compounds. This compound can also be used as an intermediate or scaffold for medicinal chemistry applications.</p>

<p>Please enquire for more information about 2-(Carboxymethyl)-4,5-dimethoxybenzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Methoxy-3-(trifluoromethyl)benzoic acid is a useful scaffold that can be used as a building block for the synthesis of complex compounds. It has been shown to react with various reagents and is a versatile building block that can be used in organic synthesis. 4-Methoxy-3-(trifluoromethyl)benzoic acid is a high quality chemical and has been classified as speciality chemicals. This product is also known by the CAS number 213598-09-5.</p>

<p>3-Fluoro-4-methoxybenzoic acid is a dipolar molecule with a fluorine atom. It has been synthesized experimentally and the yields are determined by the experimental conditions. 3-Fluoro-4-methoxybenzoic acid has two isomers, which can be differentiated by their resonances. The molecule also has an asymmetric C3(CF)2Cl group in the middle of its structure that can rotate freely.</p>

<p>2-Methoxyethyl acetoacetate is used as a raw material for coatings. It has been shown to be an effective calcium antagonist in the treatment of leukemia and other cancers. 2-Methoxyethyl acetoacetate has also been shown to inhibit the growth of HL-60 cells when it is incubated with these cells in the presence of hydrochloric acid, malonic acid, and quinoline derivatives. The reaction produces chlorine gas, which is toxic to cells.</p>

<p>Please enquire for more information about H-D-Cys(4-methoxytrityl)-2-chlorotrityl resin (200-400 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Amino-2-methoxy-dibenzofuran (3AMD) is a cytotoxic agent that is used in the treatment of bladder carcinoma. 3AMD inhibits DNA synthesis, leading to cell death by inhibiting the production of proteins vital for cell division. 3AMD has been shown to be a potent inhibitor of cyclen-dependent kinases and to induce DNA damage in human cells. 3AMD also has significant cytotoxicity against malignant cells and has been shown to inhibit the growth of tumours in mice. 3AMD may have carcinogenic potential due to its structural similarity with other carcinogens such as aniline and aminobiphenyl.</p>

<p>Please enquire for more information about 4-Methoxybenzylboronic acid pinacolester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-[2-Trifluoroethoxyphenoxy]ethyl methanesulfonate is a research chemical that is commonly used in the synthesis of enantioselective compounds. It has been clinically studied for its potential use in the treatment of prostatic hyperplasia, a condition characterized by an enlargement of the prostate gland. This compound has shown promising results in inhibiting the growth of prostatic cells and reducing symptoms associated with hyperplasia. Its enantioselective properties make it an ideal candidate for targeted therapy, allowing for more precise and effective treatment options. Researchers continue to explore the potential applications of 2-[2-Trifluoroethoxyphenoxy]ethyl methanesulfonate in various fields, including medicine and pharmaceuticals.</p>

<p>4-Methoxyphenyl boronic acid is a molecule with a hydroxyl group and a boronic acid. It is synthesized by reacting biphenyl with trifluoroacetic acid in the presence of sodium carbonate and palladium-catalyzed coupling. 4-Methoxyphenyl boronic acid has shown to bind to the receptor for fatty acids, which may be due to its structural similarity to p-hydroxybenzoic acid. The protonated form of this molecule has been shown to react with an electrophilic carbon atom and an electron-deficient alkyl or vinyl halide, resulting in ring formation. This reaction is known as the Suzuki coupling reaction.</p>

<p>2-(Chloromethyl)-4-methoxy-3,5-dimethylpyridine hydrochloride is a benzimidazole derivative. It has a chemical stability and can be used for wastewater treatment. It is also a pump inhibitor and can be used for anhydrous sodium magnesium salts. This product is synthesized from the reaction of protonated 2-bromo-4-methoxyphenol with 2,6-dimethylpyridine in the presence of hydrochloric acid. The reaction was carried out in an asymmetric synthesis using a proton transport system. 2-(Chloromethyl)-4-methoxy-3,5-dimethylpyridine hydrochloride is soluble in water and has a pH of 1 to 3. It has been shown that this product can be used as an antioxidant and as a metal chelation agent.</p>

<p>3-Amino-4-methoxybenzyl sulphone is a high quality, versatile building block that is used in the synthesis of complex compounds. It is a reagent that can be used for reactions such as the coupling of amines and carboxylic acids. 3-Amino-4-methoxybenzyl sulphone is also useful in the synthesis of pharmaceuticals and speciality chemicals. The compound has been shown to react with other substances, such as thiols and alcohols, to form new materials with interesting properties.</p>

<p>Please enquire for more information about (2R,3S)-2-[(1R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethoxy]-3-(4-fluorophenyl)morpholine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methoxy estrone is a metabolite of estrone and is produced by the enzyme 2-hydroxylase. This compound has minimal toxicity and can be used as a marker for biological processes, such as cellular transformation. 2-Methoxy estrone has been shown to inhibit the activity of acetylcholinesterase, an enzyme that breaks down acetylcholine, which is essential for neurotransmission. It has also been implicated in the regulation of angiogenic processes in vitro and in vivo. The role of 2-methoxy estrone in cancer cells is not fully understood but it may have potential as a biomarker for prostate cancer and breast cancer.</p>

<p>2-Fluoro-6-methoxybenzonitrile (2FMN) is a compound that is used as a starting material for the synthesis of other pharmaceuticals. It has been shown to bind to the acetylcholine receptor by using vibrational spectroscopy and functional theory. It also has been shown to be an effective chemokine inhibitor. Computational methods were used to optimize 2FMN's binding affinity for the acetylcholine receptor, and it was found that 2FMN binds with a dipole orientation in order to increase its binding affinity.</p>

<p>4-Amino-3-methoxypyridine (4AMMP) is a naturally occurring amino acid that can be found in the nuclei of innervated tissues. It is an inhibitor of the enzyme tyrosine hydroxylase and inhibits the synthesis of catecholamines. The concentration of 4AMMP in blood was measured by radioactivity. This agent has been used for studies on the thalamic nucleus and cortex, as well as for measuring catecholamine levels in tissue homogenates.</p>

<p>Azilsartan medoxomil is an antihypertensive drug, which is a prodrug of the angiotensin II receptor blocker azilsartan. It is synthesized through a chemical process involving the modification of the medoxomil ester, converting it into its active form upon absorption in the gastrointestinal tract. The primary mode of action of azilsartan medoxomil involves selective antagonism of the angiotensin II type 1 (AT1) receptor. By blocking the effects of angiotensin II—a potent vasoconstrictor—azilsartan medoxomil effectively reduces vascular resistance, leading to decreased blood pressure.</p>

<p>2-Methoxypropyl)amine hydrochloride (2MPPA) is a versatile building block that can be used in the synthesis of complex compounds. It is a research chemical that is used as a reagent and as a speciality chemical for the production of pharmaceuticals, agrochemicals, and other organic chemicals. 2MPPA can be used as an intermediate in the manufacture of useful scaffolds or useful reaction components. This product has CAS number 70807-90-8 and is of high quality.</p>

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<p>2-Amino-a-(methoxyimino)-4-thiazoleacetic acid is a reaction product of cefotaxime and n-dimethyl formamide. It has been shown to be an effective agent for the treatment of wastewater with a high organic content. 2-Amino-a-(methoxyimino)-4-thiazoleacetic acid also reacts with chloride ions to form cleavage products that are soluble in water, making it an ideal choice for wastewater treatment. This compound is not toxic and can be used as a drug to treat patients with infections caused by bacteria resistant to other antibiotics. 2-Amino-a-(methoxyimino)-4-thiazoleacetic acid binds to mismatched base pairs in DNA, inhibiting DNA synthesis and causing cell death by apoptosis.</p>