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Please enquire for more information about N-(2-(3,4-dimethoxyphenyl)ethyl)(4-chlorophenyl)formamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Ethoxy-4-hydroxyphenylacetic acid is a chemical compound that functions as an anaesthetic. It has been shown to produce sedation and anesthesia in animals, but not in humans. 3-Ethoxy-4-hydroxyphenylacetic acid is also a metabolite of the drug propofol, which is used as a general anesthetic.

2-Methoxyphenyl)acetone oxime is a versatile building block that can be used in the synthesis of complex compounds. It is a colourless crystalline solid with a melting point of 138°C and a boiling point of 188°C. This compound has been assigned CAS No. 43021-97-2 and is soluble in water, ethanol, acetone, benzene, chloroform, ether and ethyl acetate. The chemical structure for this compound is shown below:

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.

2-Amino-3,4,5-trimethoxybenzoic acid (2AMTB) is a potential anticancer agent that inhibits the growth of cancer cells by interfering with the epidermal growth factor receptor. It also blocks the binding of this receptor to its ligands, preventing the activation of downstream signaling pathways. 2AMTB has been shown to inhibit epidermal growth factor (EGF)-induced proliferation in vitro and in vivo. 2AMTB has also been shown to inhibit the production of reactive oxygen species and DNA damage caused by amines such as quinazolone, which are commonly found in chemotherapy drugs. These properties make it a potential anticancer drug candidate for use with other chemotherapeutic agents such as epirubicin.

Ethoxyamine hydrochloride is an organic compound that contains a hydroxyl group and a chlorine atom. It is an amine with properties of an acid. Ethoxyamine hydrochloride can be used in the treatment of metabolic disorders, such as nitro, dehydrogenase deficiency and amino acid transport disorder. The compound also has been shown to have anti-inflammatory effects, which may be due to its ability to inhibit the production of prostaglandin synthesis. This drug has been found to have no significant toxicity in humans and animals, and it has been shown to be safe for use in humans.

Please enquire for more information about Ethyl 3-((4-bromo-2-methyl-5-oxo-1-phenyl-3-pyrazolin-3-yl)methoxy)benzoate including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-(4-Methoxyphenyl)propionamide is a compound that belongs to the group of benzene amides. It is synthesized by reacting an excess of 3-bromopropionaldehyde with an amine in the presence of sodium hydroxide. This reaction produces a mixture of products, which are separated by chromatography. The yields for this reaction are approximately 90%. 3-(4-Methoxyphenyl)propionamide has been used as a biomolecular building block, and its traceless nature makes it useful in organic synthesis.
3-(4-Methoxyphenyl)propionamide can be used to synthesize alkanesulfonamides and spirolactams, which are important intermediates in chemical synthesis. 3-(4-Methoxyphenyl)propionamide also reacts with phenanthridone to produce chloride derivatives and with arenes to produce linkers.

4,4'-Dimethoxybenzhydrol is a reaction system that has been used to control experiments in which the nucleophile is an iron catalyst. The reaction system was also used to determine the reactivity of various functional groups. The linear plot of the rate of reaction versus concentration of cyclopentenes, hydroxyl group, and dehydrated functionalities indicated that these factors had little effect on the rate of reaction. However, it was found that lactams and trifluorides were able to increase the rate of reaction. Anilines were also found to be effective as they reacted with hydrogen peroxide to form phenoxides.

3,5,7,4'-Tetramethoxyflavone is a flavonoid that has been shown to have antidiabetic effects in animal studies. The mechanism of action of 3,5,7,4'-tetramethoxyflavone is not clear; however it is thought to involve the regulation of insulin sensitivity and energy metabolism. This compound has also been shown to inhibit the growth of Mycobacterium tuberculosis and other bacteria by interacting with their adenosine receptors. 3,5,7,4'-Tetramethoxyflavone binds to the basophilic leukemia cell line and inhibits its uptake of adenosine through the ccaat/enhancer-binding protein complex.

(5-Chloro-4-hydroxy-3-methoxyphenyl)acetone is a high quality reagent that is useful as an intermediate in the synthesis of complex compounds. It can be used to synthesize a wide range of fine chemicals, such as pharmaceuticals, pesticides, and fragrances. (5-Chloro-4-hydroxy-3-methoxyphenyl)acetone is also a versatile building block for the synthesis of speciality chemicals. This compound has been shown to react with other compounds to form reaction components for research purposes.

(3,5-Dimethoxyphenyl)acetone is a plant phenolic compound that has been found in many plants. It is an intermediate in the biosynthesis of lignans and a wide range of other natural products. The production of (3,5-dimethoxyphenyl)acetone by plants is induced by the presence of nitrate, chloride and/or tyrosol. This compound also represses the expression of genes involved in dextrose metabolism and carbon fixation pathways. Furthermore, it can be quantified using isotopic labelling techniques and has been detected at low levels in human urine samples.

Carbethoxysyringic acid is a reagent, complex compound, useful intermediate and fine chemical. It is also a useful scaffold for the synthesis of other organic compounds. Carbethoxysyringic acid is used in the production of speciality chemicals, research chemicals and versatile building blocks. Carbethoxysyringic acid has been shown to be an excellent reaction component in many reactions such as hydrogenation, nitro reduction, oxidation and hydrolysis.

(2,4,5-Trimethoxyphenyl)acetone is an organic compound that inhibits the replication of RNA. It was found to inhibit the activity of beta-asarone and inhibit the conversion of asarone to o-benzoquinones in cell cultures. This agent also has genotoxic effects on human liver cells. (2,4,5-Trimethoxyphenyl)acetone binds to 5-hydroxytryptamine receptors and inhibits their activities, which can lead to a decrease in serotonin concentrations. (2,4,5-Trimethoxyphenyl)acetone is a colorless liquid at room temperature with a molecular weight of 174.24 grams/mol.

4-Acetoxy-3-methoxybenzaldehyde is an antimicrobial agent that is used specifically for the treatment of lemongrass oil and eugenol. It has been shown to be effective against a wide range of microorganisms, such as Escherichia coli, Pseudomonas aeruginosa, Salmonella enterica, Staphylococcus aureus, and Streptococcus pneumoniae. 4-Acetoxy-3-methoxybenzaldehyde has been shown to inhibit the growth of bacteria by binding to the 50S ribosomal subunit. The molecule also has hydroxyl group which can react with potassium dichromate and sodium carbonate. This reaction results in the formation of 4-acetoxy-3-hydroxybenzaldehyde through an S N 2 substitution mechanism.

3-Methoxy-4-nitrobenzoic acid is a potent and selective inhibitor of aromatase that can be used for the treatment of breast cancer. 3-Methoxy-4-nitrobenzoic acid inhibits the activity of serine proteases, which are enzymes important in protein degradation and cellular signaling. This drug has been shown to inhibit the activity of many other types of kinases, and this makes it a good candidate for use as an anti-cancer agent. 3-Methoxy-4-nitrobenzoic acid also has been shown to inhibit the formation and development of brain tumors when administered via whole body or brain uptake techniques. In addition to inhibiting tumor growth, this drug can prevent metastasis by preventing circulating tumor cells from entering new tissues. The inhibition of estrogen synthesis by 3methoxy-4 nitrobenzoic acid leads to breast cancer cell death in vitro and in vivo.

2-Hydroxy-6-methoxyacetophenone is a chalcone that belongs to the group of flavonoids. It has been shown to have anticancer properties, inhibiting the growth of colorectal carcinoma cells in a dose-dependent manner. The mechanism of action for 2-hydroxy-6-methoxyacetophenone is not fully understood, but it may be due to its ability to inhibit the enzyme demethylase and induce apoptosis. This compound also has been shown to inhibit the growth of Escherichia coli and Salmonella typhimurium when used at high concentrations. 2-Hydroxy-6-methoxyacetophenone can be synthesized by reacting ethyl acetoacetate with two equivalents of methylamine in the presence of a base such as sodium methoxide or potassium hydroxide.
2-Hydroxy-6-methoxyacetophenone has also been shown to inhibit

2'-Methoxypropiophenone is a carbonyl compound that is used as a starting material in the synthesis of other compounds. It can be synthesized by reacting sodium hydroxide with diazirinyl chloride, which reacts with benzyl alcohol to produce the desired product. This chemical has been shown to bind to the DNA of bacteria and show antibacterial activity. 2'-Methoxypropiophenone has also been used to label acetophenone and other carbonyl-containing molecules for their identification.