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>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,2-dimethylhexan-1-ol is a chemical compound that contains two methyl groups. It has been identified in the atmosphere and in the chromatographic fraction of recycled oils. It is also found in the isopropyl fraction as a result of incomplete alkylation. 2,2-Dimethylhexan-1-ol is used industrially to prepare covalent adducts with tosylates, which are used as reagents for chemical ionization (CI) spectrometry and electron capture detection (ECD). The kinetic energy of 2,2-dimethylhexan-1-ol molecules was measured by atomization velocity and linear regression analysis.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>N-Ethylmethanesulfonamide is an aliphatic compound with a chemical structure containing a benzene ring and an amide group. It has analgesic properties and can be used in pharmaceutical preparations to treat pain. N-Ethylmethanesulfonamide is structurally similar to methadone, but it is not as potent. The drug binds to the opioid receptors in the brain and spinal cord, acting as a bifunctional agonist-antagonist. This binding leads to an increase in neurotransmitter release, which inhibits pain signal transmission.<br>N-Ethylmethanesulfonamide was first synthesized by chemists at Eli Lilly and Company in 1947. The synthesis was based on research performed by scientists at the Mayo Clinic, who were trying to create medicines for animal use that had analgesic effects similar to morphine but were less addictive than morphine itself.</p>

<p>2-Chloro-6-(trifluoromethyl)benzoic acid is a plant growth regulator that inhibits the ethylene synthesis. It is used to stimulate plant growth, particularly in fruit trees and vines. 2-Chloro-6-(trifluoromethyl)benzoic acid binds to an enzyme called ACC synthase that is responsible for converting acetate into ethylene. This binding prevents the formation of ACC, resulting in lower levels of ethylene production.</p>

<p>2-Methyl-3-phenyl-3,4-dihydroquinazolin-4-one is a synthetic compound that has been isolated from natural sources. It is an acetonitrile derivative of the quinazolinones, which are found in plants such as Acacia species and Moringa oleifera. 2-Methyl-3-phenyl-3,4-dihydroquinazolin-4-one has been synthesized using acetylation and ring opening methods. The synthesis of this compound can be achieved by reacting aldehydes with amines or alkylating an amine with carbon source. The reaction mechanism is initiated by the formation of an imine intermediate followed by the addition of a nucleophile to form a second intermediate that undergoes dehydration to produce the desired product. Aluminium powder is used for drying the crude product and removing water.</p>

<p>1-(Prop-1-en-2-yl)-4-(propan-2-yl)benzene is a trinitrate that is used in the polymerization of propylene. It has been shown to stabilize copolymers and bimodal polymers, as well as being able to react with different monomers. 1-(Prop-1-en-2-yl)-4-(propan-2-yl)benzene can be prepared by cationic polymerization of phenylpropionic acid, which is an enantiomer of 1-(prop-1-en-2-yl)-4-(propane -2,3,-diyldioxy)benzene. This drug also has magnetic resonance spectroscopy properties that allow it to be used as a postulated gel permeation chromatography termination agent.</p>

<p>3-Methoxythioanisole is a transfer catalyst that catalyzes the transfer of hydrogen peroxide from an alkali metal salt to an organic substrate. The reaction proceeds via a monoprotonated intermediate. 3-Methoxythioanisole can be used for the synthesis of esters, amides and nitriles. 3-Methoxythioanisole is also a hydrophilic catalyst and can be used in phase transfer catalysis. This compound is derived from the oxidation of thiophene by hydrogen peroxide, which produces a polyoxometalate as a byproduct. 3-Methoxythioanisole has been shown to be effective in catalyzing reactions between ammonium salts and phosphotungstate, yielding ammonium tungstate or hydroxylammonium tungstate as products.</p>