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>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>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>7-Fluoro-2H-chromen-2-one is a compound that has been used as a synthetic intermediate in the preparation of other compounds. It is a substrate for photodimerization and has been shown to undergo dimerization with an enantioface selectivity of up to 99%. 7-Fluoro-2H-chromen-2-one has also been used in X-ray diffraction studies to determine its crystal structure. 7-Fluoro-2H-chromen-2-one can be synthesized by fluorination of 7,8,9,10,11,12,13,14,15,16,17,18 hexahydrobenzo[1]pyrene.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Bromo-2-chloronaphthalene is a nucleophilic carbanion that is used in the synthesis of other compounds. 1-Bromo-2-chloronaphthalene can be prepared by the reaction of anhydrous hydrazine and chloroform in a solvent, followed by reaction with an acidified solution of sodium bromide. This compound can also be synthesized from 1-cyanonaphthalene, which undergoes electrophilic substitution by chlorine. 1-Bromo-2-chloronaphthalene has been used as a reagent for the reduction of anions to produce neutral molecules. The nature of this molecule is cyclic with two identical aromatic rings joined by one carbon atom. It has been shown to have antibacterial properties against staphylococcus and anthrax, as well as antifungal properties against penicillium and candida.</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>2-Methyl-3-nitrobenzonitrile is a colorless crystalline solid with a melting point of -81.8°C and a boiling point of 206.6°C. The crystal structure is shown to be an oriented, six-membered ring with hydrogen bonds and conformations that are asymmetric and dihedral. It has the molecular formula C7H5N3O2, which consists of three methyl groups and one nitro group on the benzene nucleus. 2-Methyl-3-nitrobenzonitrile is used as a starting material in organic synthesis reactions because it can undergo electrophilic substitution reactions with alkyl halides or Grignard reagents to form substituted benzenes.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-(3-Hydroxypropyl)piperidin-2-one is a volatile compound that has been found to be present in the headspace of various flowers. It is used as an analytical reagent for the analysis of volatile compounds and can be used to approximate the amount of volatile compounds in a sample. The chemical can also be used to identify volatiles by analyzing their mass spectrum. 1-(3-Hydroxypropyl)piperidin-2-one is found in the headspace of flowers, such as roses and lilacs, and has been shown to have insecticidal properties against Diptera and Calliphoridae flies. It has also been shown to have toxic properties in laboratory animals, causing death by respiratory paralysis.</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-Methyl-5-nitroquinolin-1-ium iodide is an antibiotic that has been shown to be active against a wide range of resistant microorganisms, including those resistant to hydrogen fluoride. It inhibits the production of nucleotides by binding to monoclonal antibodies and preventing their uptake. This drug also prevents the uptake of perovskite crystals by cells and interrupts chain reactions in redox potentials. The mechanism of action for 1-methyl-5-nitroquinolin-1-ium iodide is thought to be related to its ability to penetrate cell membranes and inhibit nuclear DNA synthesis. In addition, this drug has been shown to have anti-cancer properties in animal models of carcinoma cells lines, with transport properties being a possible explanation for its effects. 1-Methyl-5-nitroquinolin-1-ium iodide has basic structure with hydrogen bonds as well as water vapor and carbon dioxide, which may contribute to its effectiveness.</p>

<p>2-(2-Bromophenyl)oxirane is a sulfinyl compound that is used in the synthesis of epipodophyllotoxins. It has been shown to react with an enolate of a malonate, forming a β-unsaturated lactone and a sulfinyl group. This reaction is regioselective, giving the desired epipodophyllotoxin with the sulfinyl group on the less hindered side of the molecule. The deuterated analogues of 2-(2-bromophenyl)oxirane can be prepared by substituting one or more hydrogens with deuterium atoms. These analogues are useful for studying conformational changes in molecules because they have different nuclear magnetic resonance (NMR) spectra from their non-deuterated counterparts. 2-(2-Bromophenyl)oxirane is also useful for synthesizing styrene derivatives such as ring-opened compounds.</p>

<p>Versatile small molecule scaffold</p>

<p>2-(5-Bromothiophen-2-yl)acetonitrile is an acceptor in organic solar cells and devices. It has a molecular weight of 122.1 g/mol and a melting point of -34 °C, with a solubility of 0.0013g/mL in water. The UV absorption spectrum shows that it absorbs at wavelengths between 270-300 nm. 2-(5-Bromothiophen-2-yl)acetonitrile can be used as an electron donor for semiconducting heterojunction photovoltaic devices and has been shown to have good transport properties. This molecule also has molecular orbitals that are lower than those found in the ground state, which may be due to the presence of hydrogen bonding groups on the phenyl rings or the presence of electron donating groups such as nitro (-NO2) or cyano (-CN).</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 12-hydroxydodecanoate is a fatty acid that is produced by the reaction of dodecanedioic acid and methanol. The methyl group is attached to the carbon of the carboxyl group, yielding methyl 12-hydroxydodecanoate. The reaction mechanism for this process is similar to that of fatty acid synthesis in other organisms, where a thiodisaccharide reacts with a free fatty acid. This reaction results in the production of regiospecific methyl 12-hydroxydodecanoate. Methyl 12-hydroxydodecanoate has been shown to have potential as an antimicrobial agent due to its ability to inhibit bacterial uptake and cause cell lysis in bacteria such as E. coli K-12 and S. aureus strains.</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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Fenoprofen calcium dihydrate is a nonsteroidal anti-inflammatory drug that has analgesic and antipyretic properties. It is a prodrug that is hydrolyzed to fenoprofen in the intestinal wall and then metabolized in the liver. Fenoprofen calcium dihydrate is used for the treatment of headaches, muscle pain, menstrual cramps, arthritis, and other conditions. Fenoprofen calcium dihydrate binds to biological molecules such as enzymes or receptors at an active site. The binding of fenoprofen calcium dihydrate to the enzyme cyclooxygenase inhibits prostaglandin synthesis by preventing arachidonic acid from being converted into prostaglandins. This inhibition causes decreased inflammation and pain.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>