Ethers

<p>3,4-Dimethoxybenzyl chloride is an acetate extract that has been shown to have anticancer properties. It is also a corrosion inhibitor with the ability to inhibit fatty acid demethylation and antimicrobial agents. It has been used in pharmaceutical preparations for treating high blood pressure, as well as in the production of eugenol, papaverine and other drugs.</p>

<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 4-(Difluoromethoxy)phenylboronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3,7,4'-Trihydroxy-5-methoxy-8-prenylflavanone, (2R,3S)- is a naturally occurring prenylated flavanone, which is primarily sourced from various plant species. This compound is part of the larger flavonoid family and is often found in certain medicinal plants known for their wide range of therapeutic properties. Its structure comprises a flavanone backbone, modified by hydroxyl, methoxy, and prenyl groups that contribute to its distinctive chemical profile.</p>

<p>5-(2-Aminopropyl)-2-methoxybenzenesulphonamide is a trimethyl derivative of the aminopropyl group. It is used as a reagent to introduce hydroxymethyl groups into organic compounds. 5-(2-Aminopropyl)-2-methoxybenzenesulphonamide reacts with hydrochloric acid and an organic solvent in the preparation process. In the Friedel-Crafts reaction, 5-(2-Aminopropyl)-2-methoxybenzenesulphonamide reacts with d-alanine to form an optical isomer, which can be converted to its racemic form by ammonolysis. This compound is also used as a prostatic agent and an amide in the synthesis of benzene and phenoxymethyl alcohols.</p>

<p>Please enquire for more information about (17a)-13-Ethyl-3-methoxy-18,19-dinorpregna-3,5-dien-20-yn-17-ol 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 Nomega-(4-Methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine tert-butyl ester 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-Mercaptopropyl)trimethoxysilane is a molecule made up of three parts: a trimethoxysilane group, a trimethylsilyl group, and a mercapto group. The trimethoxysilane group is hydrophilic in nature and has an electron withdrawing effect on the molecule. The trimethylsilyl group is hydrophobic in nature and has an electron donating effect on the molecule. The mercapto group is reactive in nature and has a high redox potential. 3-Mercaptopropyl)trimethoxysilane can be used as a chemical additive to increase the stability of hydrochloric acid in water vapor by reacting with the hydroxyl groups to form stable compounds. This compound also reacts with hydrogen gas to produce methane gas, which can be used as fuel or as an alternative energy source. 3-Mercaptopropyl)trimethoxysilane also has synergistic</p>

<p>Methyl 4-methoxybutanoate is a polymorphic amine that has been shown to react with sodium salts, such as sodium methoxide, to form a new class of compounds known as oxetanes. The reaction rate is enhanced by the presence of gamma-valerolactone and the oxetane itself. It has been shown that Methyl 4-methoxybutanoate reacts with organometallic reagents to form enantiopure compounds. The kinetic profile of this compound is not yet well understood.</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 5-Bromo-2,3-dimethoxypyrazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Dimethyl 7,7'-dimethoxy-[4,4'-bibenzo[d][1,3]dioxole]-5,5'-dicarboxylate is a biocompatible polymer that can be used in the treatment of liver injury. It has been shown to have an inhibitory effect on hepatic enzyme activities and synchronous fluorescence. Dimethyl 7,7'-dimethoxy-[4,4'-bibenzo[d][1,3]dioxole]-5,5'-dicarboxylate can be used as a matrix for curcuma aromatica to remove wastewater contaminants. This polymer also has the ability to inhibit monoethyl ether-induced liver injury in low-dose groups and reduce hepatitis B virus replication.</p>

<p>Please enquire for more information about 2-Methoxy-4-amino-5-ethylthiobenzoic 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 5-(2,4-Dimethoxyphenyl)cyclohexane-1,3-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 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>Please enquire for more information about 1-(2,2-Diethoxyethyl)-1H-pyrazole 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>Please enquire for more information about 1-(4-Methoxyphenyl)-3-phenyl-1H-pyrazole-5-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,6-Dimethoxybenzoyl chloride is a halide that is used in the synthesis of other compounds. It can be synthesized by the reaction of methoxy groups with demethylation and regiospecific chlorination. This compound has been used to synthesize other substances, such as 2-chloro-2′,6′-diethoxybenzophenone. 2,6-Dimethoxybenzoyl chloride also has enzymatic activity that can be catalyzed by chromatographic science. The chloride ion is the most common anion found in living cells and it is involved in a variety of reactions. Dimethoxybenzamido and tribromide are two types of organic compounds that contain chlorine.</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>10-Methoxy iminostilbene is a photophysical that has been shown to be toxic to mouse erythrocytes and to inhibit the DNA polymerase activity of calf thymus. It has also been shown to inhibit the growth of bacteria in an industrial process. 10-Methoxy iminostilbene is insoluble in water and organic solvents, which makes it difficult to purify. 10-Methoxy iminostilbene also has high levels of impurities and is sensitive to hydrochloric acid, methylbenzene, and amines. The functional groups present on this molecule are carbonyl, nitro, hydroxyls, ethers, amides, esters, ketones.</p>

<p>Triethoxy(propyl)silane is an organosilicon compound that has reactive properties. It is a polymeric material that can be used as a component in paints, coatings, and sealants. The reaction of triethoxy(propyl)silane with sodium hydroxide solution yields hydrogen fluoride, water vapor, and hydrochloric acid. Triethoxy(propyl)silane has been shown to react with hydroxide solution to form polycarboxylic acids. The hydroxyl group on the triethoxy(propyl)silane molecule is responsible for the transport properties of this compound.</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 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-Ethyl-2,5-dimethoxy-benzeneethanamineHydrochloride is a metabolic substrate of CYP2D6. It is also an inhibitor of CYP1A2 and CYP3A4. The class of 4-Ethyl-2,5-dimethoxy-benzeneethanamineHydrochloride is not yet known. 4-Ethyl-2,5-dimethoxy-benzeneethanamineHydrochloride has been shown to cause toxicity in animal studies. Toxicity may be due to its inhibition of cytochrome P450 enzymes, which are involved in metabolism and detoxification.</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>4-Methoxyphenylacetylene is a phosphane that has been extensively studied for its reactivity in cross-coupling reactions with electron-deficient olefins. 4-Methoxyphenylacetylene has been shown to react with chlorides and form an intermediate chloride, which reacts with an olefin to form an ether. X-ray crystal structures of the reaction mechanism have been determined. The transfer mechanism involves nucleophilic attack of chloride on the phosphorus atom followed by elimination of hydrogen chloride from the phosphorus. The reaction product is an ether.</p>

<p>2-((3-Amino-4-methoxyphenyl)amino)ethanol sulfate is a potent antibacterial agent that inhibits the growth of bacteria by binding to the 50S ribosomal subunit. It is also used in dermatology, as an aminophenol, and as an ingredient in cosmetics. 2-((3-Amino-4-methoxyphenyl)amino)ethanol sulfate has been shown to be efficacious against bacterial infections caused by methicillin resistant Staphylococcus aureus (MRSA), Pseudomonas aeruginosa, Proteus mirabilis, and Klebsiella pneumoniae. This compound also has antihistamine properties.</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 2-Chloro-1-(5-methoxy-1,2-dimethyl-1H-indol-3-yl)ethanone 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-(3-Methoxyphenyl)piperidine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,2,2-Trifluoroacetic acid 1-(2,4-dimethylphenyl)-2-[(3-methoxyphenyl)methylene]hydrazide is a neuroprotective drug that belongs to the class of hydrazides. It has been shown to have neurotrophic activity in vitro and in vivo and can be used for the treatment of conditions such as diabetic neuropathy or cancer tissues. 2,2,2-Trifluoroacetic acid 1-(2,4-dimethylphenyl)-2-[(3-methoxyphenyl)methylene]hydrazide also has anti-inflammatory properties and can be used for the treatment of autoimmune diseases. The drug's mechanism of action is not fully understood but is thought to involve monoamine neurotransmitters.</p>

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

<p>3-(trifluoromethoxy)aniline is a compound that contains a trifluoromethoxy group. It has been shown to have antiproliferative effects in prostate cancer cells. 3-(trifluoromethoxy)aniline inhibits the activity of pim-1, which is important for cell proliferation and differentiation. The synthesis of 3-(trifluoromethoxy)aniline can be accomplished by one of two methods. In the first method, 3-chloroaniline is reacted with trifluoroacetic acid and bis(trimethylsilyl)acetamide in dichloromethane to form 3-hydroxy-4-chlorobenzenesulfonyl chloride (3HCBSCl). In the second method, the desired product is synthesized from 3-aminophenol and trifluoroacetic acid in acetonitrile. These two methods produce different isomers</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>Please enquire for more information about 4,5-Dihydro-5a-methoxy D-(-)-norgestrel 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-(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>3-Methoxybenzyl bromide is a synthetic molecule that belongs to the group of amides. It is used as an intermediate in organic synthesis for the introduction of ether linkages and can be used to produce other molecules with inhibitory activities. 3-Methoxybenzyl bromide has been shown to be effective against Sarpogrelate hydrochloride, which is a drug used for the treatment of hypertension. This chemical inhibits the enzyme that produces superoxide radicals and has been shown to have therapeutic effects in patients with arterial hypertension. 3-Methoxybenzyl bromide also has a nucleophilic function and can react with halides such as chlorine or bromine to form 2,5-dimethoxybenzoic acid.</p>

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

<p>4-(Trifluoromethoxy)aniline is a reactive intermediate used in the synthesis of pharmaceuticals, dyes, and pesticides. It is prepared by reacting hydrogen fluoride with aniline in the presence of an acid catalyst. 4-(Trifluoromethoxy)aniline can be used to synthesize epoxyeicosatrienoic acids, which are potent anti-inflammatory agents. 4-(Trifluoromethoxy)aniline has been shown to have a pharmacokinetic profile that is similar to those of other fluoroquinolones, but has not been studied for clinical development.</p>

<p>Please enquire for more information about 4-[Bis(4-ethoxyphenyl)methyl]piperidine 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>2-[(2-Methoxyphenoxy)methyl]oxirane is an organic compound that is used in the synthesis of other compounds and in the industrial process. It is also used as a reactant in some catalytic processes, for example, hydroxylation. 2-[(2-Methoxyphenoxy)methyl]oxirane has a hydroxyl group at the end of its structure, which makes it an organic solvent. This compound can be synthesized from chloropropane and sodium hydroxide solution. The viscosity of this compound is low and it has a developable surface. The structural formula for 2-[(2-Methoxyphenoxy)methyl]oxirane is shown below: HNCHCOCHCHOH</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>N-(p-Hydroxyphenethyl)-N-(2-bromo-5-hydroxy-4-methoxybenzyl)formamide is an anticancer drug that belongs to the class of phenethyl derivatives. It is a radiosensitizer that inhibits DNA and RNA synthesis, leading to cancer cell death. The drug has been shown to have a chiral center and two enantiomers, with the (S)-enantiomer being more active than the (R)-enantiomer. N-(p-Hydroxyphenethyl)-N-(2-bromo-5-hydroxy-4-methoxybenzyl)formamide has been shown to be effective in animal models for brain tumors and breast cancer cells. It has also been shown to be effective against leukemia cells, which are resistant to other treatments. N-(p-Hydroxyphenethyl)-N-(2-bromo-5-hydroxy-4</p>

<p>Please enquire for more information about 1-(4-Bromo-2,5-dimethoxybenzyl)piperazine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Silyl protecting group for alcohols; reagent for introducing protected C atom</p>

<p>2-Mercapto-4,6-dimethoxypyrimidine is a chemical reagent that belongs to the group of dibenzalacetone. This compound has been shown to selectively methylate benzene, dihydric alcohols, and aromatic ethers. It can be used in the chemical industry as a reagent for the production of zirconium metal oxide. 2-Mercapto-4,6-dimethoxypyrimidine has also been found to be an effective catalyst for the synthesis of dodecylbenzene from dimethylbenzene and sodium dodecylbenzenesulfonate.</p>

<p>Please enquire for more information about 2-(4-Methoxyphenyl)-2-(1-hydroxycyclohexyl)ethylamineHydrochloride 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-[(2,5-Dimethoxyphenyl)methyl]piperazine HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Apixaban is a novel, orally active, and selective factor Xa inhibitor. It is the first oral anticoagulant that has been developed to inhibit both free and clot-bound thrombin. Apixaban binds reversibly to the active site of factor Xa and inhibits factor Xa-mediated conversion of prothrombin to thrombin, resulting in an increased concentration of prothrombin in blood. Apixaban also inhibits the activity of thrombin-activated protein C (APC) that degrades fibrin clots by proteolytic cleavage of fibrinogen. This drug has a crystalline form with a particle size between 10 and 100 μm.</p>

<p>Please enquire for more information about Ethyl 3-{[(1E)-(dimethylamino)methylene]amino}-5-methoxy-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>Please enquire for more information about 3-Amino-5-(2,3,4-trimethoxyphenyl)cyclohex-2-en-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Chloro-2-methoxy-5-methylaniline is a dye molecule that is used in the synthesis of other molecules, such as diketene. It is also used as a solvent, coupling agent, and a dye molecule. This compound can be synthetically prepared by reacting naphthylamine with pyrazolone. The reaction requires catalytic amounts of polyvalent metal salts, such as zinc chloride or iron(III) chloride. The halogenation of 4-chloro-2-methoxy-5-methylaniline to produce 2,4,5-trichlorophenol can be achieved by diazotising the molecule with sodium nitrite and potassium dichromate. 4-Chloro-2-methoxy-5 methylaniline's substituents are methyl groups on the phenyl ring (Cl) and chlorine atoms (C1). Derivatives of this</p>

<p>Please enquire for more information about (-)-N-[1-(R)-Ethoxycarbonxyl-3-phenylpropyl]-L-alanine 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 (S)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Hydroxy-3-(trifluoromethoxy)benzaldehyde is a coordination compound that is used as a ligand. It has two-dimensional and crystal structures. The ligated molecule is usually coordinated to the metal ion, forming a dimer.</p>

<p>Please enquire for more information about 3-(Difluoromethoxy)benzaldehyde 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-(2-Carbomethoxyethyl)-5-(2-chlorophenyl)-thieno-1,4-diazepin-2-one 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-Methoxy retinoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Methyl trans-3-methoxy acrylate is a reactive monocarboxylic acid. It is used in the synthesis of other compounds, such as polymers and pharmaceuticals. Methyl trans-3-methoxy acrylate reacts with hydrogen chloride to form methyl 3-chloroacrylate and hydrochloric acid, and with trimethyl borate to form methyl 3-bromoacrylate. The reaction mechanism for the formation of methyl 3-bromoacrylate is similar to that for the formation of methyl 3-chloroacrylate. The reaction can be carried out in a steel or glass vessel equipped with a magnetic stirring device and equipped with an electric heating mantle or flame. The activation energies for these reactions are relatively high at 43 kcal/mol (for the metathesis reaction) and 44 kcal/mol (for the reaction with trimethyl borate). This product has been shown to react with propionate</p>

<p>Please enquire for more information about Methyl 4-methoxy-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>Please enquire for more information about N-(Ethoxycarbonylphenyl)-N'-methyl-N'-phenylformamidine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(Z)-1-Ethoxy-2-(tributylstannyl)ethene is a synthetic intermediate that is used in palladium-catalyzed cross-coupling reactions. The product of the reaction can be an acetaldehyde or a halopyridine. The yield and selectivity of the reaction depends on the nature of the reactants, solvent, and catalyst. This compound has also been reinvestigated for its ability to form an anion with electrophilic reactants.</p>

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

<p>2-Amino-3-(4-hydroxy-3-methoxyphenyl)propanoic acid is a metabolite of levodopa in the body. It is formed by oxidation of levodopa via the enzyme catechol-O-methyltransferase (COMT). This compound is used as an analytical reagent to measure levels of levodopa and its metabolites in biological samples. 2-Amino-3-(4-hydroxy-3-methoxyphenyl)propanoic acid can also be used to diagnose Parkinson’s disease, since it is produced in excess when dopamine production decreases due to the degeneration of dopaminergic neurons. The concentration–time curve for this compound can be used to calculate the clearance rate of levodopa from the blood plasma.</p>

<p>6-Methoxy-2-(4-methoxyphenyl)benzo[b]thiophene (6MBT) is a mesomorphic, acid catalyst that has been used to synthesize polyphosphoric acid. It reacts with chloride to form 6-chloro-2-(4-methoxyphenyl)benzo[b]thiophene, which can be converted to the desired product by sulfoxide. The reaction time for this process is relatively short and the yield is high. 6MBT can also be used as a semiconductor in devices such as solar cells and electronic displays. The photoelectric effect of 6MBT was demonstrated in 1972, when it was found that electron emission from a photocurrent could be obtained at room temperature. This property has been shown to be due to the molecule's absorption of light energy and subsequent conversion into electrical energy.</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>4-Methoxy-3-(trifluoromethyl)aniline is a benzene derivative that is stabilized by the methoxy and trifluoromethyl groups. The crystal structure of 4-methoxy-3-(trifluoromethyl)aniline has been determined to be orthorhombic, with space group Pbca and lattice constants a=6.541(2), b=8.829(2), c=5.744(1) Å at 100 K. This compound has a benzene ring with four methyl substituents on the phenyl ring, two of which are located on the para position. The molecule also contains two O atoms in positions 1 and 2, as well as two F atoms in positions 3 and 4.</p>

<p>Please enquire for more information about Boc-(S)-3-amino-3-(2-methoxyphenyl)propionic 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 2-Amino-3',4'-dimethoxypropiophenone 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 3-Chloro-4-methoxyphenylboronic acid 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>(R)-2-((tert-Butoxycarbonyl)amino)-3-methoxypropanoic acid (BAAM) is a potent, orally bioavailable, and pharmacokinetically well-characterized inhibitor of blood coagulation that has been shown to be effective in animal models. BAAM inhibits the activity of tissue factor (TF), an enzyme that initiates the blood coagulation cascade. TF is important for hemostasis because it is activated by contact with blood and tissue factors such as collagen or thrombin. BAAM has shown some promise as a potential treatment for thrombosis, which can lead to heart attacks and strokes.</p>

<p>4-(Benzyloxy)-5-methoxy-2-nitrobenzaldehyde (BOMBA) is an amide with affinity for microtubules. It has been shown to interact with the microtubule lattice and inhibit the polymerization of tubulin. This leads to a decrease in cell viability and cytotoxicity, as well as a decrease in tumor size. In vivo studies have demonstrated that BOMBA inhibits tumor growth by inducing thrombosis and coagulation, which results in reduced blood flow to the tumor. The mechanism of action of BOMBA is thought to be due to its ability to form sulfamates, which are known for their anti-coagulant activity.</p>

<p>1-(3’,4’-Dimethoxyphenyl)-1-propanol is a naturally occurring chemical with the molecular formula C10H14O2. It has been found in the bark of Pinus pinaster and the rhizome of Piper auritum. This compound has been shown to have an antiinflammatory effect by inhibiting prostaglandin synthesis. It also inhibits nitrosation reactions and is being studied for its potential as a cancer chemopreventive agent. 1-(3’,4’-Dimethoxyphenyl)-1-propanol is an enantiomer of 2-(3',4'-dimethoxyphenyl)propane-1,3-diol.</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>Please enquire for more information about 2-(Chloromethyl)-3-(2-methoxyphenyl)quinazolin-4(3H)-one 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-[(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>(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>4-(Trifluoromethoxy)phenylboronic acid is a boron-containing compound that has been shown to be a potent inhibitor of the histone deacetylase (HDAC) enzyme. It also has surfactant properties and can be used as a photochemical reagent. 4-(Trifluoromethoxy)phenylboronic acid is orally bioavailable and may have therapeutic potential for neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, and Huntington's disease. It also has the ability to inhibit cancer cell growth by inhibiting HDAC activity. This drug has been found to cross-couple with organosilicon compounds in order to form new compounds with potent inhibitory activity against HDAC enzymes.</p>

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

<p>Ethyl 2-(ethoxymethylene)-3-oxobutanoate is an industrial chemical that is used as a precursor to acetoacetate. It is produced by the condensation of formaldehyde and ethyl acetoacetate, which yields two molecules of ethyl 2-(ethoxymethylene)-3-oxobutanoate. This reaction can be performed in three steps, with the first step involving the addition of formaldehyde and hydrazine to acetoacetate. The second step involves heating the reaction mixture until it boils, followed by cooling and filtering. The third step requires refluxing for six hours before distilling off the liquid. Ethyl 2-(ethoxymethylene)-3-oxobutanoate can also be synthesized from orthoformic acid and ethyl acetoacetate in an experiment that produces 1 mole of product for every mole of starting material.</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>2-[(2S,3S,4S)-3-Formyl-5-Methoxycarbonyl-2-Methyl-3,4-Dihydro-2H-Pyran-4-Yl]Acetic Acid (PCA) is a natural phenolic compound that is found in olive oil. PCA has been shown to possess antioxidant and antiinflammatory properties. It also has minimal toxicity, with no adverse effects on the liver or kidney. PCA is metabolized by hydrolysis to form hydroxytyrosol and tyrosol. Hydroxytyrosol can be further metabolized to produce the aglycon 2-[(2S,3S,4S)-3-(acetyloxy)-5-(hydroxymethyl)oxolan-4-yl]acetic acid (OHA). OHA is an intermediate in the biosynthesis of erythromycin and other macrolide antibiotics such as</p>

<p>Please enquire for more information about 2-(2-Fluoro-3,4-dimethoxyphenyl)ethanamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>Please enquire for more information about 2,5-Dimethoxy-4-nitroaniline including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>This is a crystalline form of the pyrimidine derivative (S)-2-Hydroxy-3-methoxy-3,3-diphenylpropionic acid. The compound has been shown to have antiplatelet properties and is currently being developed as an antithrombotic agent. In vitro studies have shown that ambrisentan inhibits platelet aggregation, thromboxane synthesis, and leukocyte adhesion. It also reduces the levels of serum cholesterol and triglycerides in patients with chronic heart failure. Ambrisentan has been studied in clinical trials for the treatment of pulmonary hypertension associated with chronic obstructive pulmonary disease (COPD) and idiopathic pulmonary fibrosis (IPF).</p>