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>

Versatile small molecule scaffold

<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-Amino-3-chlorobenzaldehyde is a metabolite of 4-amino-1,2,4-triazole that is water soluble. Its affinity for minerals and its adsorption properties have been experimentally determined. The solubility of 4-amino-3-chlorobenzaldehyde is 6.7g/L in water at 25 degrees Celsius, and the solubility increases with increasing temperature. The adsorption isotherm was determined by using the Langmuir equation, which showed that 4-amino-3-chlorobenzaldehyde has a high affinity for both organic and inorganic matter.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-(4-Nitrophenyl)-4-phenyl-4H-1,2,4-triazole-3-thiol (NPTZS) is a potent antifungal agent that contains a thiourea moiety. It has been shown to have antibacterial activity against Escherichia coli and S. aureus in vitro. NPTZS is metabolized by n-dealkylation and is not active against Mycobacterium tuberculosis or Mycobacterium avium complex. The antimycobacterial activity of NPTZS has been demonstrated in vivo with an intraperitoneal dose of 100 mg/kg.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Bromo-5-tert-butylthiophene is a thiophene that is used in the preparation of other molecules. It has been shown to have a magnetic moment, which can be detected by electron spin resonance spectroscopy. 2-Bromo-5-tert-butylthiophene has two isomers, the cis and trans forms. The cis form is more stable due to steric interactions with the methyl groups on the benzene ring. The magnetic resonance spectrum of 2-bromo-5-tert butylthiophene shows an interaction between the substituents and the pentacene molecule, which may be due to a resonance effect.</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-Amino-N-(tert-butyl)benzamide is a chemical intermediate that can be used in the preparation of certain pharmaceuticals. This compound is synthesized through the reaction of 4-aminobenzoyl chloride and tert-butanol, which forms an amide bond. The condensation reaction can be catalyzed by either heat or acid. The product of this reaction is hydrogenated to form 4-amino-N-(tert-butyl)-N'-(chloromethyl)benzamide. This compound can also be prepared by refluxing a mixture of 4-aminobenzaldehyde and hydrazine with chloroform and hydrochloric acid.</p>

<p>Versatile small molecule scaffold</p>

<p>Research has shown that (4-Ethoxy-3-methoxybenzyl)amine (EMBA) is a potent inhibitor of bacterial growth. The alkylation of EMBA with methylamine and benzene leads to the formation of aureus, which is an antibiotic that can be used to treat staphylococcus infections. In addition, EMBA can also be methylated with hydroxylamine to form benzylamine, a compound that inhibits the synthesis of the cell wall in bacteria. These properties make EMBA an effective antimicrobial agent.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>N-(Prop-2-yn-1-yl)methanesulfonamide is a convergent synthesis of the intermediate N-(prop-2-yn-1-yl)benzenesulfonamide. The synthesis of the intermediate was achieved by reacting propargyl bromide with methanesulfonyl chloride to give N-(prop-2-yn-1-yl)benzenesulfonamide. This compound reacts with 2,4,6-trinitrobenzenesulfonic acid to afford the desired product. The functionalized alkaloid can be used as a synlett for other syntheses.</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>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>5-(Trifluoromethyl)-1H-pyrrole-3-carbonitrile is a biodegradable, synergistic effect, chlorine, organisms, chloride, pyrrole, nitrosodisulfonate, benzalkonium chloride, sodium hypochlorite and peroxides. It is recommended for use in coatings and as an additive to hydrogen peroxide formulations.<br>5-(Trifluoromethyl)-1H-pyrrole-3-carbonitrile has been shown to be effective against a wide range of bacteria including Clostridium difficile and Pseudomonas aeruginosa. 5-(Trifluoromethyl)-1H-pyrrole-3-carbonitrile has also been shown to have antiinflammatory properties that may be due to its ability to inhibit the production of prostaglandin E2 (PGE2) by blocking cyclooxygenase (</p>

<p>1-Phenylvinylboronic acid pinacol ester is a catalytic reagent that is used in organic chemistry. It has been shown to be effective in the stabilization of nanostructured materials, such as nanocrystals and organic solvents. The stability of these materials has been attributed to substituent effects on the boronic acid group. 1-Phenylvinylboronic acid pinacol ester has also been shown to be an effective catalyst for cyclopentadiene. This compound can also be used uncatalyzed, although it yields hydrogen peroxide as a byproduct. The use of 1-phenylvinylboronic acid pinacol ester in experiments can be challenging due to its instability in organic solvents.</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-acetylcyclopropane-1-carboxylate is a chiral compound that can be synthesized in an asymmetric synthesis. It has been used as a chiral building block for the synthesis of various amines and esters. The diastereoisomers of methyl 2-acetylcyclopropane-1-carboxylate are enantiomers, which means they are mirror images and cannot be superimposed on each other. The two enantiomers have different chemical and physical properties. Methyl 2-acetylcyclopropane-1-carboxylate also reacts with tryptamine to form N,N'-dimethylindole carboxamide or indole carboxamide, which is a biologically active molecule.</p>

<p>Imidazo[1,2-a]pyrimidine-2-carboxaldehyde is a biologically active compound that is synthesized through a multicomponent reaction. The synthesis of imidazo[1,2-a]pyrimidine-2-carboxaldehyde requires sodium carbonate and malononitrile as starting materials. The reactants are activated with enolizable reagents such as pyran or acetone before being subjected to the reaction. This process yields target compounds with high yields and excellent spectroscopic properties.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>