Building Blocks

<p>Versatile small molecule scaffold</p>

<p>2,2,2-Trifluoro-3'-(trifluoromethyl)acetophenone is a layered compound that has been used to test the reaction of sulfur with industrial and research nitro compounds. It is also used in the synthesis of trifluoroacetic acid catalysts. The chemical structure of 2,2,2-Trifluoro-3'-(trifluoromethyl)acetophenone was determined by analyzing its sulfur content and comparing it to other similar compounds. This compound has been shown to be an efficient catalyst system for the ionizing chemistry of trifluoroacetic acid.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Benzyl-3-phenylthiourea is a molecule that has been shown to inhibit corrosion in the presence of blood pressure. It has also been shown to be a potent inhibitor of hexamethylenetetramine, an organic compound that is used as a corrosion inhibitor. 1-Benzyl-3-phenylthiourea can be used as a biomimetic corrosion inhibitor for blood pressure and sensitivity tests. It is also capable of membrane hyperpolarization, which can be used to prevent nerve cell death from lack of oxygen and glucose.</p>

<p>Versatile small molecule scaffold</p>

<p>2,6-di(tert-butyl)-4-Nitrobenzenol is a chemical that is used as a reference standard for the gravimetric determination of sodium. It has been shown to have low toxicity in animals and environmental monitoring studies, but can be hazardous if ingested by humans. The LD50 (lethal dose) for 2,6-di(tert-butyl)-4-nitrobenzenol in Sprague Dawley rats is greater than 10 g/kg body weight. This chemical also has the potential to react with pyrimidine nucleosides and organic chemicals such as methylene chloride or urea nitrogen.</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>3,4-Dichloro-1-butene (3,4-DCB) is an industrial chemical that is used in the production of a variety of chemicals and plastics. It has been shown to be toxic to the liver and kidneys following chronic exposure, which may be due to its ability to form reactive quaternary ammonium salts. 3,4-DCB reacts with copper salt to produce hydrogen chloride gas, which can then react with water vapor in the air to produce hydrochloric acid. Hydrochloric acid is highly corrosive and can cause severe burns on contact with skin. 3,4-DCB also has the ability to isomerize into 1,2-dichloroethane (1,2-DCA), a known human carcinogen.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1,5-Dimethyl 2-bromopentanedioate is an organic compound that is a colorless solid. It is used as a synthetic intermediate for cyclen and other compounds. 1,5-Dimethyl 2-bromopentanedioate undergoes a shift reaction to form dippinine. This reaction can be catalyzed by lanthanide metals or nitroethane. The efficiency of this conversion has been studied with magnetic preparative strategies.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Chloroethanesulfonyl fluoride is a synthetic compound that belongs to the class of aliphatic chlorofluorocarbons. It is a highly reactive and useful reagent in organic synthesis, as well as in chemical biology. The chloride ion is a common functional group that can be introduced using 2-chloroethanesulfonyl fluoride. Aliphatic chlorofluorocarbons are versatile molecules with many possible applications in chemistry due to their modularity and scalability. They have been used for the synthesis of new compounds by introducing various substituents, as well as for highlighting specific chemical features such as fluorine atoms or magnesium ions, which are often difficult to detect using other analytical techniques.<br>2-Chloroethanesulfonyl fluoride has been used in x-ray crystallographic studies to investigate the structure and reactivity of magnesium oxide and magnesium chloride complexes. These studies highlight the importance of magnesium ions in chemical biology.</p>

<p>Ethyl 3-ethoxypropionate is a cycloaddition product of ethyl 3-ethoxypropanoate. It has been shown to be more chemically stable than the reactants and has an increased uptake in the reaction solution. <br>Ethyl 3-ethoxypropionate is able to undergo a cycloaddition process with diethyl succinate under conditions of high temperature and pressure, leading to the formation of methyl ethyl malonic acid. This chemical reaction takes place via an intermolecular hydrogen bonding interaction between the ethoxy group on one molecule and the ester group on the other molecule. The cyclohexane ring on each molecule also forms a hydrogen bonding interaction with its corresponding methyl or ethyl groups. Ethyl 3-ethoxypropionate is not reactive in its pure form but can undergo reactions when exposed to chemicals such as potassium hydroxide, which leads to its degradation into propionic acid and ethanol.</p>

<p>2,2,2-Trichloroethyl chlorosulfate is an organic compound that has a hydroxyl group and a chlorine in its structure. It is cytotoxic to cells and causes health effects in humans. This compound binds to the p-coumaric acid in the cell and inhibits the enzyme activity of the demethylase, which is responsible for the oxidation of p-coumaric acid to ferulic acid. This prevents p-coumaric acid from being converted into other metabolites such as dihydroferulic acid and dihydrocaffeic acid. 2,2,2-Trichloroethyl chlorosulfate also inhibits enzymes involved in the synthesis of cholesterol by competitively inhibiting HMG CoA reductase.</p>

<p>Versatile small molecule scaffold</p>