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>Dibenzyl(prop-2-en-1-yl)amine is an imidazole compound that can be prepared from the reaction of benzyl chloride with ammonia. It is a heterocyclic compound that contains a benzyl group and is used as an intermediate for the synthesis of other molecules. Dibenzyl(prop-2-en-1-yl)amine has been shown to have antiplatelet effects in vitro and may be useful in the treatment of thrombosis.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl (4-chlorobenzoyl)acetate is a nonlinear optical material with hyperpolarizability. It has a fingerprint spectrum that can be used as an identification tool and it has been shown to have diffraction properties. This compound crystallizes in the orthorhombic crystal structure and its optical properties are determined by its interconnected molecular lattice. Methyl (4-chlorobenzoyl)acetate is used in the preparation of other compounds, such as methoxymethane, which can be used to synthesize pharmaceuticals such as acetaminophen.</p>

<p>Versatile small molecule scaffold</p>

<p>1-(3-Bromofuran-2-yl)ethan-1-one is a monoterpenoid that belongs to the family of indole alkaloids. It has been isolated from natural sources and can be synthesized in the laboratory. Indole alkaloids are biologically active compounds with a variety of uses. 1-(3-Bromofuran-2-yl)ethan-1-one has shown biological activities, including antiinflammatory and antimicrobial properties.</p>

<p>Versatile small molecule scaffold</p>

<p>4-(2-Hydroxyethoxy)benzaldehyde is a growth factor that inhibits the synthesis of isonicotinic acid and erythromycin. It can be used to treat inflammatory diseases, such as arthritis, by inhibiting prostaglandin production. 4-(2-Hydroxyethoxy)benzaldehyde can be synthesized by the reaction of hydroxybenzaldehyde with 2-bromoethanol in the presence of hydrochloric acid or methyl ethyl chloride. The compound forms a deep purple solution when mixed with hydrochloric acid and turns yellow when treated with an aqueous solution of hydroxide ions. Azobenzene can form adducts with 4-(2-hydroxyethoxy)benzaldehyde, which are useful for studying the photochemical properties of this molecule.</p>

<p>1-(5-Methyl-pyrazin-2-yl)-ethanone is an acidic compound that has been detected in the headspace of foods such as meat and fish. It is formed by the reaction of hexanal with fatty acids. 1-(5-Methyl-pyrazin-2-yl)-ethanone has been detected in various foods and beverages, including meat, fish, bakery products, and fruit juices. The detection of this compound can be done using a mass spectrometer or a gas chromatograph. This chemical is analysed by solid phase microextraction (SPME) and ionization detector (GC/MS). In some cases it can also be determined by spectrometric analysis.</p>

<p>Versatile small molecule scaffold</p>

<p>5-Phenylpyrrolidin-2-one is a synthetic molecule that optimizes the catalysis of allylamines. This molecule has been shown to be a hydrolysis product of an amide and a carbonyl, and can be oxidized by sodium periodate to generate the allylamine. 5-Phenylpyrrolidin-2-one has also been found to catalyze the transfer of carbonyl groups from one molecule to another, which is useful for photocyclization reactions. This compound can also be used as an oxidant in allylamine reactions.</p>

<p>Versatile small molecule scaffold</p>

2-(4-Hydroxy-3-methoxyphenyl)-1,3-dithiolane is a metabolite of the drug product 2-[4-(hydroxymethyl)phenyl]-1,3-dithiolane. It is used as an analytical standard for drug development and in natural product research and development. The chemical properties of 2-(4-hydroxy-3-methoxyphenyl)-1,3-dithiolane are similar to those of its parent compound, but it has a smaller molecular weight. This compound has been found to be a substrate for CYP2C9 and CYP2C19 in vitro. Metabolism studies have shown that 2-(4-hydroxy-3-methoxyphenyl)-1,3-dithiolane is not converted to the parent compound or any other metabolites when incubated with human liver microsomes at 37°C.

<p>Versatile small molecule scaffold</p>