Ethers

<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>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>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>Tenofovir is a nucleoside analog reverse transcriptase inhibitor that binds to the RNA-dependent polymerase. This compound is used in combination with other antiviral agents for the treatment of HIV-1 infection and for prophylaxis against HIV-1 infection. Tenofovir has been shown to be effective against infections caused by strains of HIV-1, such as the drug resistant virus. Tenofovir is absorbed rapidly after oral administration, with a bioavailability of over 80%. The prodrug fumarate is hydrolyzed to tenofovir in vivo and this conversion occurs more efficiently in acidic conditions. Alafenamide, a prodrug of tenofovir, has been approved by the FDA as an alternative to tenofovir disoproxil fumarate (TDF) for the treatment of HIV-1 infection. Alafenamide is an acyclic nucleoside phosphonate that inhibits viral replication by inhibiting reverse</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>2,3-(Dimethoxyphenyl)acetonitrile is a chemical intermediate that is used in the synthesis of pharmaceuticals and specialty chemicals. It can be used as a reaction component and reagent for the synthesis of other chemicals. This compound has a high quality and is also a versatile building block for complex compounds. 2,3-(Dimethoxyphenyl)acetonitrile has been shown to be useful in the production of fine chemicals such as pharmaceuticals, agrochemicals, and dyes. The CAS number for this compound is 4468-57-9.</p>

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<p>3-Cyclopropylmethoxy-4-difluoromethoxy-benzoic acid is an industrial chemical that is used as a binding agent in the production of dyes, rubber, and pharmaceuticals. The compound is produced by the acylation of 3-chloromethoxybenzoic acid with cyclopropylmethanol. This reaction requires an inorganic base such as potassium carbonate or sodium bicarbonate to activate the chloride. 3-Cyclopropylmethoxy-4-difluoromethoxybenzoic acid can be used as a reactive alkylating agent for the production of amides and other organic compounds, which increases its versatility.</p>

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<p>2,4-Dimethoxyphenylmethylcarbinol is a benzene derivative that can be synthesized from 2,4-dimethoxybenzaldehyde and formaldehyde. This compound is an efficient reductant for hydrazine and has been used as a screening agent for new drugs. It is also a pharmacological active substance with anti-inflammatory properties. 2,4-Dimethoxyphenylmethylcarbinol has shown activity against carrageenan-induced rat paw edema, as well as the vessel and ultrasonic effects of irradiation.</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>3-Bromopropyltrimethoxysilane is a divalent hydrocarbon that has been used as a model compound for the study of detection methods. It has been shown to have biocompatible properties and can be used as an immobilization template molecule. 3-Bromopropyltrimethoxysilane also reacts with pyridinium ions to form complexes that are highly stable. The stability of these complexes can be attributed to the functional groups on the pyridine ring, which are more susceptible to hydrolysis than those on the silica surface. 3-Bromopropyltrimethoxysilane is a substrate for nitrate reductase enzymes, resulting in inhibition of growth at concentrations low enough not to cause cytotoxicity.</p>

<p>1-(4-Hydroxy-3-methoxyphenyl)-2-nitroethene is an experimental molecule that was not previously known to exist. The intramolecular reaction of 1,4-dihydroxynitrobenzene and glyoxylic acid yields the product. It is a phenolic compound with biological activity, which has been shown to inhibit glycosidases and alkaloids.</p>

<p>3,5-Dimethoxybenzyl bromide is a difluoro compound that has been synthesized as a potential CB2 receptor agonist. It has been shown to bind to both CB1 and CB2 receptors in cell culture. 3,5-Dimethoxybenzyl bromide has also been shown to inhibit the growth of mouse melanoma cells by inducing apoptosis and cell cycle arrest, which may be due to its ability to demethylate pterostilbene derivatives. 3,5-Dimethoxybenzyl bromide is an example of a nucleophilic agent because it can donate a proton from the hydroxyl group on the benzene ring. The chloride ion forms an ionic bond with the negatively charged oxygen atom on the benzoic acid group. This type of bond is called an ester linkage or ester bond.</p>

<p>2,4-Dichloro-5-methoxyaniline (2,4-DMA) is a trifluoroacetic acid derivative that inhibits the growth of cancer cells by interfering with cellular processes such as DNA replication and protein synthesis. It has been shown to have anticancer activity in vitro and in vivo. In addition, 2,4-DMA can inhibit the growth of cancer cells by preventing epidermal growth factor from binding to its receptor on the cell surface. A recent study showed that 2,4-DMA has anti-angiogenic properties and can prevent tumor growth by inhibiting bcr-abl kinase activity. 2,4-DMA also has an acidic property which may be due to its conversion of trifluoroacetic acid into hydrogen fluoride (HF) and hydrogen chloride (HCl).<br>2,4-Dichloro-5-methoxyaniline was approved for use in Japan</p>

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Dolastatin 15 (5S)-1-[(2S)-O-(N,N-Dimethyl-Val-Val-N-Me-Val-Pro-Pro)-2-hydroxyisovaleryl]-2-oxo-4-methoxy-5-benzylpyrrolidinium is a natural compound that has been isolated from the Indian Ocean sea hare Dolabella auricularia. It has shown significant cytotoxicity against cancer cells as well as significant immunosuppressive activities in animals. Dolastatin 15 is an analog of dolastatin 10 and has been shown to be active against hepatitis B and C virus. It also has antiinflammatory properties and may be effective in combating autoimmune diseases. The synthesis of this compound is an asymmetric synthesis with a hydroxyl group on one side of the molecule and an amide on the other side.

<p>2-Amino-2-oxoethoxy)acetic acid is a product that can be used as a transport agent in the process of extracting glycosides. It has been shown to have strong adsorption properties and is able to extract glycosides from plant material. 2-Amino-2-oxoethoxy)acetic acid has a high affinity for calcium, which is an important component in the adsorption mechanism.</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>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>5-Amino-2-methoxyisonicotinic acid is a carboxylic acid that is used in the synthesis of aminopyridines. The compound can be synthesized from formamidine acetate and diethyl dicarbonate. This process involves lithiation, followed by addition of an amine and finally conversion to the desired product with formamidine acetate. 5-Amino-2-methoxyisonicotinic acid can also be synthesized from formamide and diethyl ether. 5-Amino-2-methoxyisonicotinic acid is an analog of 2,4,6-trimethylaniline and has been shown to have similar properties to this compound, including strong basicity.</p>

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<p>Intermediate in the synthesis of lenvatinib</p>

<p>4-Fluoro-3-methoxyphenylacetone is a high quality reagent that can be used as an intermediate in the synthesis of complex compounds. This compound is also useful for creating fine chemicals and speciality chemicals, for research purposes. 4-Fluoro-3-methoxyphenylacetone has been shown to be a versatile building block in organic synthesis, with many possible applications. It can react with other compounds to create new compounds or react with itself to form new molecules. CAS No. 320338-98-5</p>

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2-[(4-Chloro-2-nitrophenyl)azo]-N-(2-methoxyphenyl)-3-oxobutanamide is a chelating agent that has been used as a control agent in the manufacture of dyes, plastics, and rubber. It is also used as an additive in paints, textiles, and paper. 2-[(4-Chloro-2-nitrophenyl)azo]-N-(2-methoxyphenyl)-3-oxobutanamide is nonvolatile, nonflammable, and does not produce toxic byproducts when heated. This compound has low molecular weight with a molecular formula of C12H13NO5Cl. The structure of this compound includes two hydroxy groups (OH), one aliphatic hydrocarbon group (CH3), one carboxylic acid group (COOH), and three chlorine atoms (Cl). This product is soluble in water

<p>Bexagliflozin is a drug that is used to treat type II diabetes in adults. It helps to control blood sugar levels by inhibiting the enzyme DPP-IV and increasing insulin release from the pancreas. Bexagliflozin has been shown to be effective in lowering blood sugar levels in patients with chronic kidney disease and cancer, as well as those with a body mass index (BMI) of 30 or higher. This drug is an oral hypoglycaemic agent that can be used for diagnostic purposes. It has also been shown to be clinically effective for the treatment of diabetic nephropathy and diabetic retinopathy. The enantiomers of bexagliflozin can be differentiated according to their pharmacological properties, which may allow for more targeted therapy.</p>

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<p>3,4',5-Trimethoxystilbene is a coumarin derivative that has been found to have inhibitory properties for mitochondrial functions. It also inhibits the production of epidermal growth factor and collagen synthesis in cells. 3,4',5-Trimethoxystilbene may be useful in treating skin conditions such as psoriasis and ichthyosis. This compound has been shown to bind to protein targets in the mitochondria and inhibit mitochondrial membrane potential by hydroxyl group reaction with proteins. 3,4',5-Trimethoxystilbene also binds to dna duplexes, which may affect its biological properties.</p>

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

<p>O-Ethoxybenzoyl chloride is a pesticide that belongs to the group of sildenafil. It inhibits the activity of prolyl endopeptidase, an enzyme that degrades the peptide hormone vasoactive intestinal polypeptide (VIP). This inhibition prevents degradation of VIP, which is important for the regulation of blood vessel tone. The compound has been shown to be effective against Sclerotinia sclerotiorum and Claviceps purpurea. O-Ethoxybenzoyl chloride has been shown to have a high level of tolerance in plants and animals. It also has been found to be safe for humans with its low toxicity levels and low acute toxicity. It is not classified as hazardous by the World Health Organization (WHO).</p>

<p>N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine is a chiral, electron deficient reagent that reacts with aldehydes and boronic esters to form products with high chemical yields. This compound can be used as a catalyst for acylation reactions, such as the synthesis of p-nitrophenol. N-Methoxymethyl-N-(trimethylsilylmethyl)benzylamine is synthesized by the reaction of trifluoroacetic acid and an amine, followed by chloroformate displacement. The product is then reacted with acylating agents in the presence of catalysts.</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-Amino-N-[2-(2,5-dimethoxyphenyl)-2-hydroxyethyl]-acetamide is a drug that has been used to treat a variety of diseases and conditions. It is an alpha adrenergic agonist that works by stimulating the alpha receptors in the body, which increase blood pressure and improve blood flow. This drug also has significant effects on energy metabolism, including the production of ATP. 2-Amino-N-[2-(2,5-dimethoxyphenyl)-2-hydroxyethyl]-acetamide is used to treat patients with congestive heart failure who are taking low doses of midodrine hydrochloride or nonsteroidal antiinflammatory drugs.</p>

<p>Please enquire for more information about Methyl 4-(3-methoxyphenyl)-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>

N-(2-Aminoethyl)-3-(trimethoxysilyl)propylamine (NAP) is a cationic surfactant that is used as a fluorescent probe to study the binding of proteins to cell surface integrin receptors. The adsorption mechanism is based on the interaction between the hydrophobic parts of the protein and the hydrophobic parts of NAP. This interaction leads to an increase in the concentration of NAP at the interface and thus an increase in fluorescence. NAP has been shown to bind human serum albumin, fatty acids, and monoclonal antibodies with high affinity. It also has been shown to bind to plasma proteins through hydrogen bonding. The optimum concentration for NAP adsorption is 1mM.

<p>7,9-Dimethoxycarbonyl-2-ethoxycarbonyl-1H-pyrrolo-[2,3-f]quinoline-4,5-dione is a chemical compound that is used as an intermediate for research chemicals. It has a CAS number of 80721-47-7 and is classified as a fine chemical with the Chemical Abstracts Service (CAS) classification code of 3272. This compound is a versatile building block that can be used in the synthesis of other compounds. 7,9-Dimethoxycarbonyl-2-ethoxycarbonyl-1H-pyrrolo-[2,3f]quinoline 4,5dione can be used to produce high quality products.</p>

<p>5-Methoxy-3,4-dihydro-2H-pyrrole is a chemical compound that contains a pyrrole ring. It can be found in the form of dehydrogenation and intramolecular hydrogen. 5-Methoxy-3,4-dihydro-2H-pyrrole has been shown to have antibacterial effects against Mycobacterium tuberculosis and other bacteria. 5-Methoxy-3,4-dihydro-2H-pyrrole also reacts with nitroacetate to form an aziridine, which is an intermediate in the synthesis of several pharmaceuticals. This chemical compound is used in the preparation of bipyrrole compounds such as naphthalene and alicyclic compounds such as nitrophenols.</p>

<p>3-(2-(3,4-Dimethoxybenzoyl)-4,5-dimethoxyphenyl)pentan-2-one is an alkylene that is produced by the reaction of hydrazine with 2,3,4-trimethoxybenzoic acid. This molecule has been shown to have anxiolytic properties in animal studies and hydrolyzes to form ethylene glycol. 3-(2-(3,4-Dimethoxybenzoyl)-4,5-dimethoxyphenyl)pentan-2-one also has a hydrolysis product of tofisopam. Tofisopam is an organic acid that has been used as an antidepressant for the treatment of anxiety disorders.</p>

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<p>Potassium 4-methoxycinnamate is a fine chemical that is used as a versatile building block in the synthesis of complex compounds. It can be used in research and as a reagent or speciality chemical. It is also a useful building block for high quality, useful intermediate, and reaction component. Potassium 4-methoxycinnamate can be used as a scaffold to synthesize compounds with diverse applications such as pharmaceuticals, polymers, and agrochemicals.</p>

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<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>

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>Diffraction is a technique that is used to measure the angles of the reflections from a crystal or other material. Single-crystal x-ray diffraction (SCXRD) is one form of diffraction that uses a single crystal to generate an image. Diffraction was first observed in 1807 by English scientist William Hyde Wollaston and French physicist Joseph von Fraunhofer. Diffraction can be used to determine the structures of ionic, linear, or annulated frameworks, such as those found in 1,2-Difluoro-4,5-dimethoxybenzene. The molecular geometry and relative orientation of the atoms in these frameworks can be determined through diffraction. This technique is often used to characterize polymers with cyclic structures such as penicillin and cyclic voltammetry. <br>Diffraction studies have shown that 1,2-Difluoro-4,5-dimethoxybenzene has a hydroxylase</p>

<p>1,3-Bis(methoxycarbonyl)-2-methyl-2-thiopseudourea (BMTC) is a novel anticancer agent that has been synthesized to be water soluble and also has significant cytotoxicity. BMTC is believed to exert its anticancer activity by binding to the colchicine binding site on tubulin which is involved in microtubule dynamics. The antitubulin effect of BMTC results in inhibition of cell division and growth. BMTC also inhibits cancer cell proliferation and migration. It has shown significant cytotoxicity against human prostate cancer cells and ovarian cancer cells, as well as inhibiting tumor xenografts in mice.</p>