Building Blocks

<p>2-tert-Butyl-1,3-benzoxazole is an organic compound that belongs to the group of benzoxazoles. It can be synthesized by a variety of methods, including oxidative coupling of 2-tert-butylbenzothiazole with benzene or 1,2-dibromobenzene, or by the intramolecular cross-coupling reaction between 2-(2'-hydroxyphenyl)benzothiazole and methyl iodide. The compound has been shown to be an excellent ligand for palladium(II). This ligand can be used in asymmetric synthesis strategies to generate optimal yields of benzoxazoles from simple starting materials.</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>N-(1,3-Thiazol-2-yl)pyridin-2-amine is a tyrosine kinase inhibitor that can be used to treat cancer. It was found to inhibit the growth of tumor cells by interfering with their ability to make new proteins. The drug also has a low molecular weight and a high solubility in water, which makes it suitable for intravenous administration. N-(1,3-Thiazol-2-yl)pyridin-2-amine inhibits protein kinases through competitive binding to the ATP binding site on the enzyme's active site. It has an analog profile that includes low molecular weight and high solubility in water, making it suitable for intravenous administration. Additionally, it has been shown that this drug is selective for receptor tyrosine kinases over other types of protein kinases (e.g., serine/threonine), while still exhibiting cross covalent coupling with piperazine</p>

<p>2-Tributylstannylthiophene is a molecule that is used in organic synthesis. It is synthesized by the cross-coupling of 2-bromothiophene and tributyltin chloride. This molecule has been shown to be thermochromic, meaning that it changes color with a change in temperature. The color changes from yellow at lower temperatures to red at higher temperatures. 2-Tributylstannylthiophene has been shown to have optical properties, such as fluorescence and absorption, which are dependent on its molecular structure. It also has chemical properties, such as acidity, which can be altered by substituents on the carbon atoms of the molecule. 2-Tributylstannylthiophene can be used as a monomer for an organic material with constant optical properties because it does not undergo any reactions when exposed to inorganic acids or bases.</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-(Pyrrolidin-1-yl)pyridine is a chiral compound that belongs to the group of nucleophilic compounds. It can be synthesized in two different configurations, as either the erythro or threo isomer. The synthesis of 2-(pyrrolidin-1-yl)pyridine requires an asymmetric synthesis and involves the reaction of an acyl chloride with 2,6-dichloropyrimidine. The erythro isomer has been shown to have receptor activity at cb2 receptors and has been shown to reduce inflammation in animal models. The threo isomer has been shown to have reduced activity at cb2 receptors and does not show anti-inflammatory properties.</p>

<p>1-(4-Methoxyphenyl)pyrrolidine is an amide that is structurally related to buspirone and diazepam. It has been shown to have a high affinity for serotonin receptors. 1-(4-Methoxyphenyl)pyrrolidine has been found to be an antagonist of diazepam in the brain, and it also inhibits the binding of lidocaine to the sodium channel. In addition, 1-(4-Methoxyphenyl)pyrrolidine has pharmacological properties similar to those of procaine and lidocaine, which are used as local anesthetics. This drug was found to be acutely toxic in rats, but not at levels that would be harmful for humans.</p>

<p>Methyl 2-methylazulene-1-carboxylate is a natural product that is found in the leaves of the "Mentha" species. It has shown anti-inflammatory, analgesic and antipyretic properties. Methyl 2-methylazulene-1-carboxylate is a cost effective analog of azulene and is used in medicinal preparations. It can be obtained by thermolysis of an ether or vinyl ether with a lactone. This compound has been shown to have optical (light) activity when cycloaddition reactions occur at the double bonds of the molecule. Tropolones are related compounds that also show this optical property.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>