Building Blocks

<p>2-[(4-Methoxyphenyl)methoxy]acetaldehyde is an antifungal compound that belongs to the group of cyclic compounds that are synthesized from phenols. This compound is used in the synthesis of a number of synthetic molecules, including allyl alcohol and esters. 2-[(4-Methoxyphenyl)methoxy]acetaldehyde has been shown to be a reagent for the catalytic asymmetric synthesis of ethylidene derivatives. It also has anticancer activity, which may be due to its ability to inhibit cell growth and induce apoptosis.</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>1,2,3,4-Tetrazolo[1,5-a]quinoline-4-carbaldehyde is an imidazole derivative with antibacterial activity. It inhibits bacterial growth by binding to the β-unsaturated ketones in the cell wall and preventing their synthesis. 1,2,3,4-Tetrazolo[1,5-a]quinoline-4-carbaldehyde has been shown to be effective against Streptococcus mutans and other organisms. It is also a substrate for chlorination reactions and can be used as a catalyst in organic synthesis 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>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-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)acetate is a benzyl ester that was synthesized by the reaction of chloroformate and methyl ester. Methyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)acetate is a functional group that can be used as a linker in solid phase synthesis. It has been shown to undergo alkaline hydrolysis to produce dicarbonate, yielding high yields. This compound also reacts with benzyl alcohols to form methyl esters, which are important organic compounds.</p>

<p>Versatile small molecule scaffold</p>

<p>4'-Hydroxy-biphenyl-3-carboxylic acid (4HBCA) is a chiral molecule with an acidic character. 4HBCA has been shown to be a potent regulator of the mesomorphic properties of 3-hydroxybenzoic acid. It has been shown that the compound destabilizes the mesomorphic state, which may be due to the presence of hydroxyl groups in both the phenyl and carboxylic acid moieties. The addition of 4HBCA to biphenyl at room temperature results in lamellar crystals. These crystals are birefringent and have a negative optical rotation. 4HBCA also induces dehydrogenation reactions with polyfluoroalkyl compounds.</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>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>2,5-Dibromo-3,4-pyridinediamine (DBPD) is a heterocyclic compound that is used in the preparation of diazo compounds and as a precursor to 2,5-dichloropyridine. The reaction between DBPD and magnesium sulfate produces an unstable intermediate that can be stabilized by adding pyridine or quenching with diazole. This reaction process is used for the industrial production of 2,5-dichloropyridine.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Iodo-2-methylbutan-2-ol is an aliphatic compound that undergoes hydrogen atom transfer reactions. It has been shown to be a selective transfer agent for the synthesis of substituted alkenes in the presence of halides and hydroalkylation. 4-Iodo-2-methylbutan-2-ol is also an unactivated, catalytic system that can produce predictable reactions with electrophiles.</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>Bromo-2-methyl-2H-1,4-benzoxazin-3(4H)-one is a chemical compound that can be used as an intermediate in organic synthesis. It is a protonated form of the base molecule and has a neutral pH. Bromo-2-methyl-2H-1,4-benzoxazin-3(4H)-one has been shown to damage the surface of skin and other tissues due to its ability to react with proteins and lipids. This chemical also damages cell membranes by disrupting their lipid bilayers, which leads to less efficient cellular function.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Spiro[3.5]nonane-6,8-dione is a synthetic target molecule that belongs to the class of organic compounds called epoxides. This molecule can be synthesized by a process that begins with the addition of acetonedicarboxylate to an epoxide followed by the addition of hydrogen peroxide. The resulting product is an epoxide and hydrogen peroxide mixture, which can be converted into spiro[3.5]nonane-6,8-dione in a second step with an acrylate or peroxide. Spiro[3.5]nonane-6,8-dione has been used as a research intermediate in the synthesis of other molecules.</p>

<p>Versatile small molecule scaffold</p>

<p>1,1,3-Trioxo-2,3-dihydro-1,2-benzothiazole-5-carboxylic acid is a carboxylic acid that can be prepared by sulfonation of 1,1,3-trioxo-2,3-dihydrobenzthiazole with sulfur dioxide and hydrochloric acid. This compound has been used as a sweetener in the food industry. It is also used as a precursor for other compounds such as 2,2′-[1,4]oxazinane and 2-[(pyridinium methylsulfonyl)amino]-N-(pyridinium methylsulfonyl) acetamide. The decarboxylated form of this compound is an iron chelator that binds to ferric ion. This compound reacts with copper ions to give copper complexes like 1-[(pyridinium methyls</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>