Building Blocks

<p>Versatile small molecule scaffold</p>

<p>4-Chloro-2-iodo-1-methylbenzene is an organic compound that belongs to the class of methylanilines. It can be synthesized by reacting methyl iodide with 4-chlorobenzene. The product is a diazonium salt, and it reacts with sodium nitrite in water to form the corresponding hydrazone. This chemical has been used as a precursor in the synthesis of other compounds.</p>

<p>Versatile small molecule scaffold</p>

<p>Cyclopentyloxybenzene is a bidentate ligand that binds to the active site of cyclic AMP phosphodiesterase, inhibiting the enzyme's ability to break down cyclic AMP. Cyclopentyloxybenzene also has an antioxidant effect, which may be due to its ability to prevent the production of reactive oxygen species. This compound emits light when it reacts with deuterium atoms. When deuterated, cyclopentyloxybenzene does not react as quickly and has a higher yield than non-deuterated compounds. It also has transport properties that make it ideal for reactions in organic solvents. The reaction time is slower than other bidentate ligands, but the energy efficiency is greater due to the reduced activation energy required for chemical reactions.</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-Ethoxy-2-phenylacetonitrile is a quinoline derivative that has been shown to inhibit the HIV virus. This drug binds to the CCR5 receptor on the surface of human T cells and prevents the virus from entering. 2-Ethoxy-2-phenylacetonitrile also shows antiviral activity against herpes simplex virus and cytomegalovirus (CMV). The drug also has chemokine activity, which may be important for its anti-inflammatory properties.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Benzyl-1H-pyrrole is a chemical compound that belongs to the group of aldehydes. It can be produced by irradiation of trans-stilbene and has been shown to react with acetals, yielding acetal adducts. The reaction of 3-benzyl-1H-pyrrole with benzaldehyde in the presence of sodium ethoxide yields an acetal. The spectrum for 3-benzyl-1H-pyrrole shows two peaks at 2.2 and 2.6 ppm; the first peak corresponds to the methylene protons, while the second peak corresponds to the methyl protons in the aromatic ring. The fragmentation pattern for 3-benzyl-1H-pyrrole is characterized by a series of three peaks at m/e = 55, 62, and 69 corresponding to loss of hydrogen atoms on C2, C3, and C4 respectively. This compound has also been shown</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>