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>4-(tert-Butyldimethylsilyloxy)benzaldehyde is a molecule that belongs to the group of anionic compounds. It is synthesized from phenol and tert-butyldimethylchlorosilane. This compound is used in the synthesis of paclitaxel, which has been shown to be effective against breast cancer cells. 4-(tert-Butyldimethylsilyloxy)benzaldehyde can also be used as a precursor for other functionalized molecules, such as copolymers. This compound undergoes copolymerization with various other monomers, such as vinyl acetate, acrylate esters, and acrylic acid derivatives to form polyesters. 4-(tert-Butyldimethylsilyloxy)benzaldehyde reacts with fluoride ion or chloride ion in solution to produce colorimetric changes. It also reacts with butyllithium to form primary alcohols.</p>

<p>(2-Aminopyrimidin-5-yl)methanol is a research chemical commonly used in the field of chemistry. It is a versatile compound that can undergo various reactions, including methylation using chlorotrimethylsilane. This compound is often employed in laboratory settings for its ability to form new chemical bonds and facilitate the synthesis of complex organic molecules. Researchers value (2-Aminopyrimidin-5-yl)methanol for its unique properties and its potential applications in drug discovery and other scientific endeavors.</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-Phenyl-1H-pyrrole-3-carbaldehyde is a ligand that binds to the chiral metal center of the metallocene. The steric and electronic properties of this ligand determine its ability to activate the metallocene. 1-Phenyl-1H-pyrrole-3-carbaldehyde has a methyl group, which can undergo regiospecific substitution by a methyl group. This ligand also has an anion, which can be used for coordination with the chiral metal center. The methyl groups in 1-Phenyl-1H-pyrrole-3-carbaldehyde are not stereospecific and can be replaced by other groups without affecting the activity of the ligand.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>The compound is soluble in water, methylmagnesium chloride and ether. It has a high yield of 71% at 50 degrees Celsius. The reaction is not affected by the presence of acid halides and decarboxylating agents. 1-(5,6-Dichloropyridin-3-yl)ethan-1-one reacts with pyridine to form 3,4-dichloro-N,N'-dimethylpyridine. This reactant is used as a diluent for medicines and as an efficiency reagent in the manufacturing of dyes.</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>Methyl 2-((tert-butoxycarbonyl)amino)thiazole-5-carboxylate is a six membered, planar molecule with two methyl groups and two carbonate groups. It is a dimer with two centrosymmetric molecules that are connected by hydrogen bonds. This compound has a molecular weight of 184.1 g/mol, melting point of 115-117 °C and boiling point of 205 °C.</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>SPhosPdG3, a bifunctional ligand, is capable of binding to the kinetochore-microtubule interface and inhibiting mitosis in cells. SPhosPdG3 binds to the kinetochore-microtubule interface and inhibits mitosis by altering the spindle checkpoint. The ligand has been shown to bind to the bromodomain on proteins that are involved in cancer development and progression, such as CDK4/CDK6 and BRD2. SPhosPdG3 has been shown to have inhibitory potency for these protein kinases in vitro. This compound may be useful for treating cancer through targeting these pathways.</p>

<p>DavePhos-Pd-G3 is a catalyst that can be used in the synthesis of alkenes by difunctionalization of cyclopropanes. This reaction is stereoselective and gives high yields. DavePhos-Pd-G3 is a heterogeneous catalyst with a phosphorous-gold (Pd) core and can be used in the synthesis of alkenes. The Pd core has been shown to catalyze the oxidative addition of cyclopropane to give an alkene in good yield and excellent stereoselectivity. The Pd core is prepared from a mixture of PdCl2, HCl, and elemental gold (Au).</p>