Ethers

<p>4-Methoxy-tetrahydro-2h-pyran-4-carboxylic acid is a fine chemical that belongs to the group of research chemicals. It is a versatile building block and useful intermediate in organic synthesis. 4-Methoxy-tetrahydro-2h-pyran-4-carboxylic acid has been used as a reagent for the preparation of the compound 5,5'-dithiobis(4,4'-dimethylvaleronitrile) (CAS No. 1010836-49). This compound has been shown to be an effective antiviral agent against HIV.</p>

<p>3-Bromo-2,6-dimethoxy-5-nitrobenzoic acid is a chemical component that can be used as a reagent or building block for the synthesis of other compounds. It is also an intermediate in the synthesis of pesticides and pharmaceuticals. 3-Bromo-2,6-dimethoxy-5-nitrobenzoic acid is a versatile compound with many applications in organic chemistry. This chemical has been shown to have high purity and can be used as a reaction component or reagent in research and development laboratories.</p>

<p>Please enquire for more information about 2,5-Dimethoxy-4-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 3-(tert-butyl)-4-((2-hydroxy-3-methoxyphenyl)methylene)-1-phenyl-2-pyrazolin-5-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-(3-Benzyloxy-4-methoxyphenyl)-2-nitroethene (1BMN) is an ethanamine that has a skeleton of five benzene and one methoxybenzene rings. It is an analogue of lamellarin, which has been shown to have efficient synthetic and biological properties. 1BMN is biologically active as a lamellarin analog and may be useful for the treatment of diseases such as cancer, malaria, hypertension, hyperglycemia, hypercholesterolemia, and ulcerative colitis. 1BMN is synthesized from 2-nitroethanol by reacting with 3-bromobenzaldehyde in the presence of sodium hydroxide. This reaction results in the formation of 1BMN in high yield with few side reactions.</p>

<p>6-Methoxy-2-naphthaldehyde is a nonsteroidal antiinflammatory drug that belongs to the class of naphthalenes. It inhibits the formation of inflammatory prostaglandins, which are mediators of pain and inflammation. 6-Methoxy-2-naphthaldehyde has been shown to have cytotoxic effects on cancer cells and in vitro studies have shown that it can induce cell lysis. It has also been shown to be a potent fluorescence probe for use in biological applications. This compound binds to human serum proteins by hydrogen bonding interactions, which may affect its pharmacokinetic properties. In addition, this compound has been shown to inhibit the activity of detoxification enzymes such as CYP 2C9 and 2D6 at high concentrations, which may lead to unwanted side effects such as nausea or vomiting. The molecular docking analysis of 6-Methoxy-2-naphthaldehyde with the active site of human liver alcohol dehydrogen</p>

<p>(2-Methoxyphenoxy)acetonitrile is a versatile building block that has been used in the synthesis of fine chemicals, complex compounds, research chemicals, reagents and speciality chemicals. It is a useful building block for high quality pharmaceuticals. (2-Methoxyphenoxy)acetonitrile can be used as a reaction component or scaffold to synthesize organic molecules with interesting biological activities.</p>

<p>Trans-2,5-dimethoxy-4'-nitrostilbene is a molecule that belongs to the class of polycyclic aromatic compounds. It is used as a versatile building block in organic synthesis, and is also an intermediate for the production of other compounds. Trans-2,5-dimethoxy-4'-nitrostilbene has been shown to be effective in the preparation of various pharmaceuticals such as diazepam and chloramphenicol. It is also used in research chemicals and speciality chemicals. The structure of trans-2,5-dimethoxy-4'-nitrostilbene can be described as a bicyclic compound with two phenyl rings joined by an oxygen bridge. Trans-2,5-dimethoxy-4'-nitrostilbene has CAS No. 552938 4 and molecular weight of 268.81 g/mol.</p>

<p>Hexamethoxymethylmelamine (HMMM) is a polyvinyl-based polymer that can be synthesized by the cationic polymerization of hexamethoxymethylmelamine. HMMM has been shown to have a high water permeability, making it an excellent candidate for use in wastewater treatment. It also has biocompatible properties and can be chemically stable under harsh conditions, making it suitable for use in various applications.</p>

<p>2'-Hydroxy-2,4,4',6'-tetramethoxychalcone (HTMC) is a bioactive substance that has been shown to have anticancer properties. HTMC has been shown to have allopathic effects in a statistically significant manner and has been used in traditional herbal medicine for centuries. The mechanisms of action are not well understood but may be due to its ability to inhibit the activity of arjunic acid and flavonoids. HTMC is found in plants such as tropical trees and herbs from India, including Acacia catechu and Tinospora cordifolia. It also has pharmacological properties, which may be due to its derivates that are isolated from these plants. HTMC shows no adverse effects on humans when taken orally at doses up to 1 g/day for 28 days.</p>

<p>3-(3,4,5-Trimethoxyphenyl)propionic acid (TMPPA) is a monocarboxylic acid that is structurally related to the amino acid lysine. It has been shown to have antinociceptive effects in animals and humans. TMPPA inhibits the production of prostaglandins and nitric oxide, which are inflammatory mediators that induce pain. TMPPA also has nociceptive properties in rats when given intraperitoneally or intrathecally, showing a reduction in locomotor activity. This compound also inhibits protein synthesis by binding to the ribosomal protein S6 kinase-1 (RSK-1), which is the target of many antibiotics used for cancer treatment. TMPPA binds to human serum albumin with high affinity and specificity, suggesting it may be useful as an agent for targeting human blood cells or as an antiobesity drug.</p>

<p>Lobetyolin is a phenolic compound that has been found to be an inhibitor of monoamine oxidase. Lobetyolin is an acetylated derivative of 4-hydroxy-3-methoxyphenylacetonitrile. It has been shown to inhibit bacterial growth in vitro, with the exception of Mycobacterium tuberculosis and Mycobacterium avium complex. The optimal reaction time for lobetyolin is 3 hours at a pH between 7 and 8, with a yield of 66% at room temperature. Lobetyolin reacts rapidly with amines, alkylating them as it undergoes oxidation by hydrogen peroxide. Lobetyolin also reacts slowly with dopamine and aldehydes, but more readily with chlorides, yielding lobetyrine and chloroacetaldehyde respectively.</p>

<p>4-Methoxy-2,3,5-trifluorobenzoic acid is a versatile building block that can be used in the synthesis of complex compounds. It is a high quality chemical that can be used as a reagent or speciality chemical in research. This compound has been shown to have many uses including as an intermediate for the synthesis of other chemicals and as a reaction component. 4-Methoxy-2,3,5-trifluorobenzoic acid can also be used as an important scaffold in the design of new drugs.</p>

<p>2-(3-Methoxyphenoxy)-2-methylpropanoic acid is a reagent, useful intermediate and speciality chemical. It is a versatile building block for the synthesis of complex compounds. This product has CAS No. 140239-94-7, which is a fine chemical with high quality. It is an essential reaction component for the preparation of many other valuable chemicals in the laboratory.</p>

<p>1,2,3-Trimethoxybenzene is an organic compound with the formula CH(OCH)3. It is a colorless liquid that is soluble in water and polar organic solvents. The compound has been shown to undergo Friedel-Crafts reactions with amides to form diazonium salts, which are then hydrolyzed to give glycol ethers. It can be used as a structural probe for methyltransferase inhibitors such as trimethyl. 1,2,3-Trimethoxybenzene can also undergo demethylation and transfer reactions with nucleophiles such as hydrochloric acid or glycol ethers. The chemical shifts of 1,2,3-trimethoxybenzene in NMR spectra are characteristic for the methoxy groups that are present on the benzene ring.</p>

<p>2-Hydroxy-5-methoxybenzaldehyde is a colorless, water-soluble liquid that has been used as a chemical intermediate in the synthesis of pharmaceuticals. It is also an antiinflammatory agent that inhibits acetylcholinesterase. 2-Hydroxy-5-methoxybenzaldehyde binds to copper ions by means of hydrogen bonding interactions and forms stable complexes with nitrogen atoms such as amides, nitriles, and hydrazones. 2HMB has been shown to have antiinflammatory activity in animal studies. This compound has a redox potential of -0.8 V, which indicates it can be oxidized by strong oxidizing agents or reduced by strong reducing agents.</p>

<p>Trans-3,4,5,4'-tetramethoxystilbene is a potential anti-cancer drug that inhibits the growth of prostate cancer cells. It has been shown to inhibit the activity of cytochrome P450 enzymes and induce apoptosis in prostate cancer cells. Trans-3,4,5,4'-tetramethoxystilbene also has an inhibitory effect on angiogenesis and induces apoptosis in breast cancer cells. This compound is not readily absorbed from the gastrointestinal tract and has low bioavailability due to its chemical properties. Trans-3,4,5,4'-tetramethoxystilbene binds to DNA and inhibits transcription by competitive inhibition of RNA polymerase II and III.</p>

<p>2-(4-Methoxyphenoxy)-2-methylpropanoic acid (methoxymethyl) is a versatile building block with a variety of applications in synthesis. It is used as an intermediate in the preparation of pharmaceuticals, agrochemicals, and dyes. Methoxymethyl has been shown to be useful as a reagent for research and as a speciality chemical. This compound can also serve as a reaction component or scaffold in the synthesis of more complex compounds.</p>

<p>6-Bromo-2,3-dimethoxybenzoic acid is a synthetic chemical that has been shown to have antibacterial activity. It has been shown to inhibit the growth of bacteria by binding to the imine group in the bacterial cell wall and preventing its synthesis. 6-Bromo-2,3-dimethoxybenzoic acid has also been shown to be synthesised from 2,3-dimethoxybenzoic acid and bromine. This compound is a benzophenanthridine alkaloid that inhibits protein synthesis and cell division.</p>

<p>2,5-Dimethoxybenzamide is a potent inhibitor of the enzyme DECATENASE. This enzyme plays an important role in the biosynthesis of the aromatic amino acids phenylalanine and tyrosine. 2,5-Dimethoxybenzamide has been shown to have anticancer activity in vitro and in vivo. Remoxipride is a synthetic drug that competitively inhibits the action of benzodiazepines on GABA receptors by binding to them with high affinity. It was developed as an antipsychotic agent but was never marketed for this indication due to its adverse effects on motor coordination. Remoxipride has also been shown to have estrogenic activity, which may be due to its ability to bind with high affinity and inhibit the enzyme aromatase, which converts testosterone into estradiol.</p>