Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-[4-(Propan-2-yl)cyclohexyl]ethan-1-one is an organic compound that contains a cyclohexane ring with a 1,4-dioxane ring attached. It has the molecular formula C9H16O and it has 12 carbons. The structural formula for this molecule is shown below.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3,3-Dimethyl-1-(2-phenylethyl)urea is a tertiary amine that can be synthesized by reacting isobutyraldehyde with ammonia. It has a molecular weight of 188.2 and a melting point of 117°C. The conformational energy of 3,3-dimethyl-1-(2-phenylethyl)urea has been determined using the electrostatic functional theory. This method was used to study the effect of the solvent on the conformational energy of 3,3-dimethyl-1-(2-phenylethyl)urea by calculating the interaction energies between molecules in different solvents.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Phenylcycloheptan-1-one is a chemical compound that has been shown to have affinity for the piperidine receptor site in rat brain, which may be due to its structural similarity to piperidine. This chemical is a cyclohexanone derivative and is used as a medicinal agent. 4-Phenylcycloheptan-1-one has been shown to be an effective catalyst in asymmetric syntheses of cyclohexanones and other compounds, including catalytic asymmetric syntheses of phenylcycloheptanes.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Ethyl 4-[(tert-Butoxycarbonyl)amino]-3-oxobutanoate (4BAA) is a synthetic compound that has been shown to have anticancer activity in vitro. It reversibly inhibits DNA synthesis and cell proliferation by inhibiting the enzymatic activity of DNA polymerase II and topoisomerase II. 4BAA also has an inhibitory effect on the proliferation of tumor cells, which may be due to its ability to inhibit protein synthesis. In vivo studies have shown that this compound accumulates in tumor tissue, but not in normal tissues, at concentrations that are 10-fold higher than those found in plasma. This agent also inhibits the growth of fibroblasts and other non-malignant cells in vitro.</p>

<p>3-(Chloromethyl)benzofuran (3CBF) is a heterocyclic compound that can be used in solar cells. It has the capability to absorb light and generate electricity. 3CBF has fluorescence properties, which means it can emit light when exposed to ultraviolet radiation. The optical properties of 3CBF have been studied by voltammetry and cyclic voltammetry methods. 3CBF also has optical properties that are sensitive to pH changes and is soluble in potassium hydroxide. Solar cells containing 3CBF have high photovoltaic yields because of its high quantum efficiency, low cost, and stability in air.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about Ethyl 4-(Dimethylamino)-2-oxobut-3-enoate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-(Quinolin-3-yl)propanoic acid is an antihyperglycemic drug that has been shown to have an antihyperglycemic effect in rats. It was found to inhibit the activity of propionic acid, a precursor of glucose, and also reduced the levels of glucose in the blood. 3-(Quinolin-3-yl)propanoic acid is an intermediate in the synthesis of other drugs such as ampicillin and cefuroxime.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>8-Bromoquinolin-2(1H)-one is an organic compound that inhibits the production of inflammatory substances in the body. It is a long-chain alkene and a synthetic substance that is used to prepare pharmaceuticals. 8-Bromoquinolin-2(1H)-one has been shown to have anti-cancer properties, as well as an inhibitory effect on inflammation. The drug is synthesized by reacting benzonitrile with bromine and ammonia in a reaction system. 8-Bromoquinolin-2(1H)-one inhibits the synthesis of prostaglandin E2 (PGE2) by inhibiting cyclooxygenase and lipoxygenase enzymes. It also binds with high affinity to the enzyme phospholipase A 2 (PLA 2 ), which results in a rapid hydrolysis of phospholipids and production of arachidonic acid, which leads to increased levels of PGE2.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Ethylbenzamide is a synthetic, catalytic intramolecular reaction. The product of this reaction is an amide and benzamide which are two important classes of organic compounds. The mechanism of this reaction is that the intramolecular addition of 2-ethylbenzoyl chloride to the nitrobenzene in the presence of base yields the desired product. This reaction is catalyzed by lithium metal, which activates the nitro group and provides a strong electrophile for nucleophilic attack. It has been shown that mechanistic control experiments show that there is no difference in reactivity between electron-rich and electron-poor alkyl groups in benzonitriles or amidoximes. In asymmetric synthesis, it has been shown that lithiation followed by amidoxime formation with chiral diamine ligands leads to high enantioselectivity.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl 5-bromo-2-naphthoate is a Grignard reagent that reacts with a variety of organic compounds. It has been used in the synthesis of polymers, such as polyvinyl chloride, and yields higher yields than other Grignard reagents. Methyl 5-bromo-2-naphthoate can also be used to synthesize butyllithium, which is an organolithium compound that is commonly used as a strong base in organic synthesis. This reagent can be prepared by reacting magnesium with chloroform and bromine. Methyl 5-bromo-2-naphthoate also reacts with acetylene to form ethynyl bromide. The elimination reactions between methyl 5-bromo-2-naphthoate and hydrogen halides produce trifluoromethyl bromide or trifluoromethyl iodide.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>6-Methoxy-2-naphthonitrile is a phenolic compound that has been synthesized by reacting cyclobutane with nitroethane. It has antihypertensive activity. Phenols are aromatic compounds that can be found in many plants, animals, and microorganisms. They have an oxygen atom attached to a hydroxyl group (-OH) and are classified as either simple or polycyclic. 6-Methoxy-2-naphthonitrile is a simple phenol that contains one ring of six carbon atoms. The molecule can also be classified as an aldehyde because it contains the -CHO functional group on the carbon adjacent to the hydroxyl (-OH). The nmr spectra of 6-methoxy-2-naphthonitrile indicate that it is chiral, which means it can exist in two forms that are non superimposable mirror images of each other. This property makes the</p>

<p>Versatile small molecule scaffold</p>

<p>3-(4-Bromophenoxy)propan-1-ol is the chemical compound with the formula CHBrOH. It is a colorless liquid that is soluble in organic solvents. 3-(4-Bromophenoxy)propan-1-ol has been used as an estrogenic agent, and to enhance the solubility of triazole and tetrahydrofuran. It also functions as a fluorescence quencher, and can be used for cancer treatment or diagnosis. 3-(4-Bromophenoxy)propan-1-ol can be optimized for its acceptor properties by varying the substituents on the phenyl ring.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl 3-amino-5-hydroxybenzoate is a chemical compound that belongs to the group of antibiotics and is used as a selective agent in microbiological cultures. It is not active against Gram-positive bacteria, but has been shown to be selectively active against Verticillatus. Methyl 3-amino-5-hydroxybenzoate prevents the synthesis of DNA by inhibiting the enzyme DNA polymerase. It also inhibits mitomycin C production by Streptomyces, which may be due to its ability to inhibit aldehyde dehydrogenase. Methyl 3-amino-5-hydroxybenzoate is an antibiotic that was first isolated from Australian soil samples.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Formylpyrrolidine-2-carboxylic acid is a compound that belongs to the group of pyrrolidines. It is soluble in water and has a strong odor. 1-Formylpyrrolidine-2-carboxylic acid is used as an intermediate for pharmaceuticals, agrochemicals, and dyestuffs. Impurities include chloral, organocatalysts (e.g., l-amino acetate) and peroxides (e.g., hydrogen peroxide). Other impurities include l-glutamic acid and l-threonine, which are naturally occurring compounds found in plants. 1-Formylpyrrolidine-2-carboxylic acid can be obtained by evaporation of its filtrated form or by reacting with chloral hydrate in the presence of potassium amide.</p>