Ethers

<p>2-Bromo-4-methoxybenzaldehyde is a cyclic, stereoselectively eliminable, acrylate that can be used in the asymmetric synthesis of sulfamidate and lactam. It can also be used to synthesize quinoline derivatives with aluminium chloride. This product has been shown to yield good yields when reacted with functional groups such as halides and nature. 2-Bromo-4-methoxybenzaldehyde is found in biomolecular reactions.</p>

<p>Please enquire for more information about 4-(Methoxycarbonyl)bicyclo[2.1.1]hexane-1-carboxylic acid 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 4-Bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Chloro-2-(chloromethoxy)ethane is an acyclic nucleoside phosphonate that is used as a HIV integrase inhibitor. It binds to the HIV RNA genome and prevents the integration of viral DNA into the host cell's genome, which blocks the replication of HIV. 1-Chloro-2-(chloromethoxy)ethane has been shown to be more potent than other acyclic nucleoside phosphonates in vitro and in vivo. This drug also inhibits herpes simplex virus type 1 (HSV1) thymidine kinase activity, which is essential for viral DNA synthesis. This drug has potential antitumor activities against certain tumor cells due to its ability to inhibit cell proliferation and induce apoptosis through inhibiting rna synthesis.</p>

<p>1,3-Dimethoxy-2-(2-methoxyphenoxy)propane-1,3-diol (DMMP) is a natural product with antioxidant properties. It has been shown to be a potent inhibitor of the epidermal growth factor receptor (EGFR), and also inhibits the activity of the response elements for EGFR. DMMP is also a potent inhibitor of proliferation in human cancer cells and can inhibit the growth of tumour cells that are resistant to methotrexate. DMMP is a precursor to protocatechuic acid, which has been shown to have anti-herpes virus effects. DMMP has been shown to decrease the rate of second order reactions through its ability to react with carbonyl groups on proteins. This reaction leads to an increase in stability and decreases the rate of protein degradation by proteases. A mutant strain was found that can produce this compound without any external stimulus, making it ideal for use as an antibiotic against bacterial</p>

<p>N-Methoxy-N-methylacetamide is a nucleophilic amide that can be synthesized by the reaction of acetamide with methylmagnesium chloride. It has been used to synthesize an enantiopure derivative of 2-aminopropanol, which is used in the synthesis of potent antitumor agents. N-Methoxy-N-methylacetamide has shown potent anticancer activity in mice and rats. This molecule exhibits a carbonyl group that can act as an enolate, which is a reactive intermediate within chemical reactions. The nucleophilic attack on this carbonyl group leads to intramolecular hydrogen transfer, producing a more stable product.</p>

<p>4-Iodo-2-methoxypyridine-3-carboxaldehyde is a disubstituted compound that has insulin-like properties. It inhibits the activity of the insulin receptor, which may contribute to its insulin-like growth factor effects. This inhibitor also targets the protein kinase, which is responsible for the response of cells to insulin. 4-Iodo-2-methoxypyridine 3 carboxaldehyde has been shown to inhibit IGF1R and malonate ion, and it may have potential as an oral treatment for diabetes.</p>

<p>Please enquire for more information about 4-Benzyloxy-3-methoxy-N-methylphenethylamine hydrochloride 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 5[(R)-(2-Aminopropyl)]-2-methoxybenzenesulfonamide hydrochloride 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 2-Methyl-4-(trifluoromethoxy)bromobenzene 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 4-Formyl-3-methoxy-phenyloxymethyl polystyrene resin (200-400 mesh) 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 3-[4-(4-Methoxyphenyl)piperazin-1-yl]-3-oxopropanenitrile 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 rac-3-hexadecanamido-2-methoxypropan-1-ol phosphocholine monohydrate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Methoxy-5-methylsulfonylbenzoic acid is an organic compound that can be used as a pharmaceutical intermediate. It has been used to synthesize diagnostic agents and drugs such as isradipine and sarpogrelate hydrochloride. 2-Methoxy-5-methylsulfonylbenzoic acid is also used as an intermediate in the synthesis of bortezomib, a drug that inhibits the proteasome. This product contains impurities that may interfere with its use as a pharmaceutical preparation. The flow rate of this product is sensitive to changes in temperature and pressure.</p>

<p>Please enquire for more information about 3-(Difluoromethoxy)aniline 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 3,4-Dimethoxy-Benzamidine HCl 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 6-(2,3,4-Trimethoxyphenyl)-1,5,6,7-tetrahydro-4H-indazol-4-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>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.</p>

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

<p>(±)-N-Methyl-p-methoxyamphetamine (MEM) is a synthetic cannabinoid that is used as an ingredient in the manufacture of designer drugs. MEM can be detected by gas chromatography and mass spectrometry, although it is not possible to distinguish MEM from other synthetic cannabinoids by these methods. MEM produces no significant adverse effects on human liver, but may have serious adverse effects on the heart and blood vessels. The drug can be found in urine samples with a chemical ionization detector or electrochemical detector. <br>The analytical method for MEM detection is based on liquid chromatography-tandem mass spectrometry (LC/MS/MS). The LC/MS/MS technique separates and identifies compounds by creating ions through the use of an electric field. This method has been shown to accurately detect MEM, while also eliminating false positives due to its specificity.</p>

<p>Please enquire for more information about 1-Benzyl-5-ethoxy-1H-indole-3-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(R)-5-(2-Aminopropyl)-2-methoxybenzenesulfonamide is an amide. It is a hydrochloric acid salt that can regulate the reaction system and introduce filtration, which can be used to separate the components of the reaction system. The kinetic and chiral properties of this compound are derived from Friedel-Crafts reactions with phosphites and Friedel-Crafts reactions with d-alanine. (R)-5-(2-Aminopropyl)-2-methoxybenzenesulfonamide can also catalyze ammonolysis and catalysis with phenoxy.</p>

<p>Please enquire for more information about 5-Bromo-2-methoxyphenethylamine hydrobromide 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 3-Methoxy-7a-methyl-estra-2,5(10)-dien-17-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-(4-Methoxybenzyl)piperazine is a chemical compound that has been shown to have inhibitory activities against cancer cells. It also shows potential for the treatment of type 2 diabetes and Alzheimer's disease. The mechanism of action is not well understood, but it may be due to its ability to induce mitochondrial biogenesis and insulin sensitivity. 1-(4-Methoxybenzyl)piperazine has also been shown to improve memory in rats with spontaneous dementia, similar to the effects of donepezil (a drug used for Alzheimer's disease). 1-(4-Methoxybenzyl)piperazine can be taken orally or administered via injection.</p>

<p>2(2-Ethoxyethoxy)ethanol is a glycol ether that is used as a substrate film in analytical methods, such as thin layer chromatography. It has been shown to be toxic to the liver and kidney, but not the heart. 2(2-Ethoxyethoxy)ethanol is also an experimental solubility data and can be used to measure the hydrophobic effect of organic compounds. This substance has high values for solubility, which may be due to its glycol ester type. 2(2-Ethoxyethoxy)ethanol does not show toxicity to the heart when administered orally or by inhalation, but does show toxicity to the liver and kidney at high doses.</p>

<p>Please enquire for more information about 2-Hydroxy-2-(3,4-dimethoxyphenyl)ethylamine hydrochloride 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 Methyl 4,5-dimethoxy-1-methyl-1H-indole-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5,6-Dimethoxy-1H-indazole is a phosphite that has been used as an intermediate in the synthesis of some pharmaceuticals. It has been shown to have hypotensive effects in rats and depressant effects in mice. The nitro group on 5,6-dimethoxy-1H-indazole can be reduced to an aminopropyl group by reaction with chloride and methyl alcohol or piperazine. This reaction produces two products: 1) a chloro compound that is not pharmacologically active and 2) a methylated product that retains all the original activity of 5,6-dimethoxy-1H-indazole. 5,6-Dimethoxy-1H-indazole also interacts with DNA by binding to nitrous oxide (N2O), which is present at high levels in clinical settings such as dentists' offices. Nitrous oxide reacts with 5,6-dimethoxy-1H</p>

<p>3-Amino-4-methoxypyridine is a molecule that has been shown to have anesthetic activity. It has been shown to inhibit the uptake of glycogen by glioblastoma cells and decrease the rate of glycogen synthesis in these cells. 3-Amino-4-methoxypyridine also inhibits the production of ATP in cardiac muscle cells, which may be due to its ability to inhibit glycogen synthase kinase-3 (GSK3) and glycogen synthase. This drug also inhibits cancer cell growth by inhibiting protein synthesis, as well as inflammatory disease progression by inhibiting NFκB activation and cytokine production. 3-Amino-4-methoxypyridine can be synthesized from aminopyridines such as isonicotinic acid or nicotinic acid, which are oxidized with hydrogen peroxide and sodium nitrite in the presence of a base catalyst.</p>

<p>Alpha-(1,1,2,2,2-Pentafluoroethyl)-omega-[Tetrafluoro(Trifluoromethyl)Ethoxy]-Poly[Oxy[Trifluoro(Trifluoromethyl)-1,2-Ethanediyl]] - Average MW 2000 (FTFEPA) is a fluorinated compound that is a monofluorophosphate. It is used as an electrolyte in nonaqueous systems. FTFEPA has been shown to be effective in reducing the corrosion of metals such as magnesium and aluminum.</p>

<p>5-[3-Methoxy-4-(4-methoxy-benzyloxy)-benzyl]-pyrimidine-2,4-diamine is a monoclonal antibody that blocks the signal of CTLA-4, a receptor on T cells. It has been shown to be effective in inhibiting skin cancer and primary breast cancers. This drug also has immunomodulatory effects and can be used to treat autoimmune diseases. 5-[3-Methoxy-4-(4-methoxy-benzyloxy)-benzyl]-pyrimidine-2,4-diamine binds to ctla-4 with high affinity and specificity, preventing the interaction of ctla-4 with its ligands such as CD80 (B7.1) and CD86 (B7.2). This prevents the activation of T cells by antigen presenting cells and suppresses the immune response.</p>

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

<p>4-(Butoxymethyl)-2-methoxyphenol is an antimicrobial agent that has been shown to be effective against Candida glabrata. It is a non-ionic surfactant with a C8 alkyl chain, which is derived from the reaction of butyl alcohol and phenol. 4-(Butoxymethyl)-2-methoxyphenol can be used in oral care products such as toothpaste or mouthwash. This product also has a control analysis for sodium citrate and root powder, which may be due to its fatty acid and magnesium salt content.</p>

<p>2-(4-Methoxyphenyl)benzothiazole is a hydrogen-bond acceptor that is activated in the presence of an electron-withdrawing group. It has been shown to have anti-fungal properties and inhibitory properties against bacteria. 2-(4-Methoxyphenyl)benzothiazole also inhibits the activity of topoisomerase, which is an enzyme that controls DNA supercoiling and uncoiling, as well as DNA replication. The mechanism of this inhibition is not known, but it is thought to be due to the ability of 2-(4-methoxyphenyl)benzothiazole to form hydrogen bonds with the active site cysteine residues on topoisomerase I. 2-(4-Methoxyphenyl)benzothiazole also has been shown to be photophysical in nature, absorbing light at wavelengths of 350 nm and 480 nm and emitting light</p>

<p>2,3,4-Trimethoxyaniline (2,3,4-TMXA) is a methoxylated monophenolic compound. It has been shown to be effective at disrupting the microtubules in cancer cells and is believed to work by inhibiting the enzyme topoisomerase II. 2,3,4-TMXA also inhibits dopamine synthesis and blocks the amine uptake system in cancer cells. This agent has been shown to be an effective anticancer drug for human serum at nanomolar concentrations.</p>

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

<p>2-Bromoethoxy-tert-butyldimethylsilane is a conjugate that has been shown to have anticancer efficacy in vivo. It is a pyrimidine derivative and inhibits the viral enzyme RNA polymerase, thereby inhibiting viral replication. 2-Bromoethoxy-tert-butyldimethylsilane also inhibits glyceraldehyde 3-phosphate dehydrogenase, which is an enzyme that catalyzes the conversion of glucose into glyceraldehyde 3-phosphate and plays an important role in glycolysis. The compound has been shown to be active against mouse tumors, which are associated with endogenous retroviruses. The compound has also been shown to inhibit gapdh, an enzyme involved in energy metabolism and cancer therapy.</p>

<p>2-Fluoro-5-methoxyaniline is a high quality reagent that is used as an intermediate in the synthesis of various complex compounds. The CAS number for this chemical is 62257-15-2 and it has been shown to be useful as a building block for the synthesis of fine chemicals, speciality chemicals, and research chemicals with many different uses. It is also a versatile building block that can be used in reactions involving amines, alcohols, thiols, and nitriles. 2-Fluoro-5-methoxyaniline may also be used as a reaction component in organic syntheses.</p>

<p>Ethoxylated hydrogenated castor oil is a surfactant that is often used in vitro to study cell nuclei. It has been shown to have an optimum concentration of 0.025% (v/v) in vitro assays. Ethoxylated hydrogenated castor oil also has the ability to prevent radiation-induced damage by stabilizing the cell membrane and preventing leakage of cellular contents, which can lead to cell death. This surfactant has been shown to increase synchronous fluorescence in vitro, and it is not toxic when applied topically at concentrations up to 10%. Ethoxylated hydrogenated castor oil has been found to inhibit the growth of infectious bacteria such as Chlamydia pneumoniae and Helicobacter pylori, and it may be a potential drug for treating cardiac dysfunction.</p>

<p>Please enquire for more information about 3-[2-(Ethoxycarbonyl)-1-methyl-1H-indol-3-yl]propanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ethoxyphenylboronic acid is a triazine compound which inhibits inflammation by inhibiting the kinase that catalyzes the phosphorylation of arachidonic acid. It also inhibits lipid kinase, which is involved in the metabolism of lipids, and it has been shown to inhibit cancer cell growth through hydrogen bond interactions with DNA. Ethoxyphenylboronic acid has been shown to have anti-inflammatory properties and may be useful for the treatment of inflammatory diseases such as arthritis. The compound can also inhibit hydrogen peroxide-induced oxidative damage in cells, due to its ability to release intracellular glutathione.</p>

<p>4-Methoxybenzene-1,3-diamine sulfate (4MBD) is a chemical substance that inhibits the activity of cytochrome P450 enzymes. It has been shown to inhibit the activity of rat liver microsomal p-450 enzymes, and is used in studies on the effects of chemicals on protein synthesis. When 4MBD is administered to rats at dietary concentrations, it causes an increase in thyroid hormone levels and a decrease in renal function. The enzyme inhibition caused by 4MBD may be due to its ability to acylate amines, which are located near the active site of the enzyme. Linear regression analysis showed that there was a strong correlation between dietary concentrations and the inhibition of protein synthesis caused by 4MBD.</p>

<p>3,4-Dimethoxythiophenol is a chemical compound that is used as a fluorescence probe to study biological functions in cells. It reacts with hydroxyl groups and other reactive sites on proteins, including sulfhydryl groups, thiols, and amines. 3,4-Dimethoxythiophenol has been shown to inhibit the viability of cancer cells (e.g., prostate cancer cells) by interfering with the function of dehydrogenase enzymes. 3,4-Dimethoxythiophenol also inhibits growth of microglia (cells that protect neurons) in vitro. This inhibition is due to the production of reactive oxygen species by the microglial cells. The chemical structure of this compound includes a hydroxyl group and two methoxy groups.</p>

<p>S-(+)-alpha-Methoxy-alpha-(trifluoromethyl)phenylacetic acid chloride is an optical, amide, and epoxidation derivatizing agent that is used to chiralify amines. It is a liquid at room temperature with a molecular weight of 123.87 g/mol. This chemical reacts with alcohols to form esters, which can be identified by their different retention times in chromatography. It also reacts with hydroxyl groups to form ethers and esters, as well as hydroxyls on other molecules such as amino acids, peptides, and proteins. S-(+)-alpha-Methoxy-alpha-(trifluoromethyl)phenylacetic acid chloride has been used for the synthesis of bisoprolol from metoprolol and triethylphosphite.</p>

<p>Dimethoxymethane is a colorless liquid with a sweet odor.  Dimethoxymethane has been used as an intermediate in organic synthesis, as well as a solvent for various reactions.</p>

<p>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.</p>

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

<p>4-Methoxyphenyl chloroformate is a reactive chemical that can be used to synthesize amides, esters, and anhydrides. It reacts with nucleophiles such as chloride or hydroxide to form an intermediate product. This intermediate product then reacts with the desired molecule to form the desired final product. 4-Methoxyphenyl chloroformate has shown selectivity for binding to opioid receptors, including mu and delta subtypes. This chemical may be used in the synthesis of antibiotic drugs that have similar receptor subtypes. 4-Methoxyphenyl chloroformate also has been shown to modulate G protein signaling pathways in cells, which may lead to improved pharmacokinetic properties.</p>

<p>Please enquire for more information about Methyl 3-methoxypicolinate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-[(2-Methoxyphenoxy)-methyl]-2-oxazolidinone is a pharmacological agent that is structurally similar to rapamycin. It has been shown to inhibit the production of creatine kinase in rat liver microsomes and has been used in studies on degenerative diseases. 5-[(2-Methoxyphenoxy)-methyl]-2-oxazolidinone inhibits the activity of polymerase chain reaction (PCR) by binding to the DNA polymerase and blocking the extension of an oligonucleotide primer. It has also been shown to be toxic to humans, as it can cause fatty acid accumulation and a clinical response. In addition, this drug is enantiopure, meaning that it is composed of only one type of molecule with a specific configuration. The analytical chemistry for this drug includes gas chromatography (GC) and high performance liquid chromatography (HPLC).</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>2-Bromo-6-methoxypyridin-3-amine is a perovskite that has been shown to have a high photoluminescence quantum yield and can be used in solar cells. This compound interacts with both the ligands and the acceptors, boosting the efficiency of these compounds. The 2-bromo-6 methoxypyridin-3 amine is a semiconductor with an electron affinity of 1.9 eV and a band gap of 1.6 eV. It has been shown to be efficient as a photoluminescent material in nanocrystals.</p>

<p>3-(Chloromethyl)-4-methoxybenzaldehyde is a natural product that can be extracted from the rhizomes of the plant. It has been shown to have antibacterial activity in laboratory experiments and has been used in traditional medicine for the treatment of fungus infections. 3-(Chloromethyl)-4-methoxybenzaldehyde is an imidazolylmethyl derivative with a hexane structure. It reacts with hydrochloric acid to form a molecule called chloromethylation, which is also known as an esterification reaction. Piperazine acts as a catalyst in this reaction, increasing its scalability and making it suitable for large-scale production. The compound exhibits radical scavenging activity, which may be due to its ability to donate electrons or hydrogen atoms to free radicals.</p>

<p>Please enquire for more information about 7-[(4Methoxyphenyl)methyl]-5-methyl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione 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 7-Methoxy-1,2,3,4-tetrahydronaphthalen-2-ylamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(7S)-7-Amino-1,2,3,10-tetramethoxy-6,7-dihydro-5H-benzo[g]heptalen-9-one is a hydroxylated analog of demecolcine. It has been shown to be an effective antimicrobial agent with proteolytic and hypoglycemic effects in mice. 7SATM is able to inhibit the activity of human macrophages. This drug has also been shown to have diagnostic potential by binding to a monoclonal antibody that recognizes the myeloperoxidase enzyme on the surface of neutrophils.</p>

<p>4-Ethoxyphenylboronic acid is a boron-containing compound that has been shown to have potent antiviral activity. This compound is synthesized from adipose tissue and optical properties of the phenoxazine derivative are studied in order to find an efficient process for solid-phase synthesis. 4-Ethoxyphenylboronic acid has been shown to inhibit triglyceride lipase and fatty acid, which may be an important drug target. It has also been found to have potent antagonistic effects on fatty acids.</p>

<p>4-(4-Hydroxymethyl-3-methoxyphenoxy)-butyric acid (HMPA) is a synthetic compound that is used in the production of butyric acid. It is also used as a reagent in the preparation of enzymes and enzyme preparations, such as serine proteases. HMPA has been used as an intermediate in the synthesis of ribulose, which is a sugar molecule found in plants. The structure of this compound can be determined by FTIR spectroscopy and by X-ray crystallography. HMPA has been shown to have hydrogen bonding between its molecules, which may account for its stability. Hydrogen bonding accounts for the solidity of this compound and its resistance to heat and solvents.</p>

<p>5-Ethoxy-2-mercaptobenzimidazole is a corrosion inhibitor that has been shown to inhibit the growth of cancer cells by causing them to undergo apoptotic cell death. It also has a protective effect on nerve cells, as evidenced by its ability to prevent the neurotoxic effects of hydrochloric acid. 5-Ethoxy-2-mercaptobenzimidazole is synthesized from 2-(2'-hydroxyethoxy)benzaldehyde and ethyl chloroformate in the presence of sodium chloride and hydrochloric acid. It is then converted into 5-ethoxy-2-mercaptobenzimidazole with sodium hydroxide.</p>

<p>Please enquire for more information about 8-[(1E)-2-(3,4-Dimethoxyphenyl)ethenyl]-1,3-diethyl-3,9-dihydro-1H-purine-2,6-dione 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 3-(Difluoromethoxy)nitrobenzene including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl (2E)-3-(4-hydroxy-3-methoxyphenyl)acrylate is a natural compound, which belongs to the group of ferulate esters. It has been shown that methyl (2E)-3-(4-hydroxy-3-methoxyphenyl)acrylate inhibits the activity of esterases, which are enzymes that hydrolyze esters. This inhibition leads to an accumulation of ferulic acid in the blood, which is associated with bowel disease. Methyl (2E)-3-(4-hydroxy-3-methoxyphenyl)acrylate has been shown to be effective against murine hepatoma cells and polymorphonuclear leucocytes, which are white blood cells that can be found in the blood and other tissues. The inhibitory effect on these cells may be due to its ability to bind to ferulic acid and caffeic acids.</p>

<p>4-Chloro-6-methoxyquinoline is an inhibitor of bacterial DNA gyrase. It has antibacterial activity against Gram-positive and Gram-negative bacteria, including Staphylococcus aureus, Enterococcus faecalis, and Pseudomonas aeruginosa. 4-Chloro-6-methoxyquinoline is a synthetic compound that was reinvestigated for its antibacterial activity. It has been shown to be effective in the treatment of Staphylococcal infections. The mechanism of action may involve inhibition of topoisomerase II or interference with the synthesis of DNA by binding to the enzyme bacterial DNA gyrase. Quinidine and cinchonidine are quinine derivatives that have been found to inhibit bacterial DNA gyrase. These compounds are found in the bark of Cinchona species, which includes Cinchona ledgeriana, Cinchona officinalis, and Cinchona succirub</p>

<p>Please enquire for more information about N-2-Ethoxyethyl-Val-Ala-anilide including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>Please enquire for more information about 3-(4-Methoxybenzoyl)acrylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>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>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>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>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>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>Please enquire for more information about (4S,5R)-3-Benzoyl-2-(4-methoxyphenyl)-4-phenyl-5-oxazolidinecarboxylic acid 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 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>2,2-Dimethoxyacetaldehyde is an inhibitor of the enzyme DNA polymerase. It has been shown to inhibit replication of the herpes simplex virus type 1 and 2 (HSV-1, HSV-2) in cell cultures. 2,2-Dimethoxyacetaldehyde has also been shown to inhibit the replication of HIV in cells and is a potential antiviral agent. This compound is also used as a building block for other drugs such as amide and ester hydrochloride. It is synthesized from 2,2-dimethoxypropane and formaldehyde with a two step process that starts with an asymmetric synthesis reaction between formaldehyde and methoxide ion followed by an ester hydrochloride formation reaction with methylamine. The product can be purified by recrystallization from water or acetone solution.</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>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>

<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>

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<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>

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<p>Sulfamethoxypyridazine is a sulfa drug that inhibits bacterial growth by inhibiting the synthesis of folic acid, which is essential for DNA and RNA production. It has been shown to be effective in the treatment of urinary infections and infectious diseases. Sulfamethoxypyridazine interacts with other drugs, such as oral contraceptives, to increase their blood levels. This drug also has a matrix effect on urine samples, which can be used to detect the presence of bacteria. The matrix effect is due to its hydrophobic nature and ability to form aggregates with other compounds. Sulfamethoxypyridazine is used in wastewater treatment plants as an analytical method for nitrogen atoms.</p>

<p>2-Iodo-5-methoxybenzoic acid is a macrocyclic compound that has been synthesized in the Wittig reaction. It was first prepared by catalyzed intramolecular aryl demethylation of 2-iodo-5-nitrobenzoic acid, followed by coupling with methyl vinyl ketone. The cytotoxic activity of this compound is due to its ability to inhibit the synthesis of protein and DNA and induce apoptosis. This molecule has been shown to be effective against liverworts and ethers.</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>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>

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<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>

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<p>Ethyl 4-methoxyphenylacetate is a fatty acid that is synthesized by the condensation of aniline and pyrrole. It has been shown to inhibit the growth of bacteria, such as Salmonella typhi and Staphylococcus aureus, in vitro. The inhibition of bacterial growth is thought to be due to its ability to react with hydrogen fluoride, which results in the formation of reactive oxygen species and nitrogen radicals. This compound also inhibits the production of tyrosinase in human skin cells, which may be beneficial for individuals with acne. Ethyl 4-methoxyphenylacetate has been shown to be safe for use in clinical trials.</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>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>

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