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>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>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-(Prop-2-yn-1-yl)-1H-indole is a n-alkyl indole that has been shown to catalyze the interphase.</p>

<p>4-Ethylquinoline is an organic compound that has a number of uses, including as a stabilizer in polyvinyl chloride and as a chloroformate. It also has an important role in the synthesis of 8-hydroxyquinoline. The hydroxy derivative is used as a reagent for the stereoselective synthesis of heterocycles and trifluoromethylthiolation.<br>4-Ethylquinoline can be synthesized from butyraldehyde and 1,2-dichloroethane. This reaction proceeds with high stereocontrol, giving 4-ethylquinoline in high yield.<br>4-Ethylquinoline is stable to heat and acid, making it useful for many chemical reactions. One use is as an intermediate for the synthesis of 8-hydoxyquinoline, which can be used as a marker for DNA synthesis in calf thymus tissue or bacterial DNA gyrase.</p>

<p>1,4-Dimethyl 2-hydroxy-2-methylbutanedioate is an allylating agent that modifies the amino acid lysine residues in proteins. It has been shown to be effective in the treatment of skin lesions caused by Staphylococcus aureus and other bacteria because it inhibits bacterial growth through an antimicrobial effect. 1,4-Dimethyl 2-hydroxy-2-methylbutanedioate also has been used as a precursor for the synthesis of vitamin D3. This compound is metabolized in mammalian cells to form cysteamine, which is further converted to S-(1,4-dimethylpentadienoyl)cysteamine (DMPE). The resulting product can be used as a functional group on collagen or malic acid. 1,4-Dimethyl 2-hydroxy-2-methylbutanedioate also is used for modifications of mucocutaneous tissues such as skin and oral muc</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-Chloro-2-methyl-5-nitrophenol is a white solid with an alkaline reaction. It is used in the production of sulfonated dyes, as well as in the manufacture of certain drugs and pesticides. 4-Chloro-2-methyl-5-nitrophenol can be made industrially by the elimination of toluene under acidic conditions. This product also reacts with nitric acid to form a radical intermediate that adds to a phenyl group, forming a nitro group at position 2 on the ring structure, yielding 4-(2'-methylpropyl)-phenylamine. This compound can also be made by reacting 2,4,5-trichlorophenol with phosphorus pentachloride or thionyl chloride. The resulting chlorinated compound is then oxidized to produce 4-(2'-methylpropyl)-phenylamine and HCl gas.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Dimethylamino-2,2-dimethyl-1-propanol (DMAP) is a chemical compound that is used as a catalyst in organic synthesis. DMAP is used for the preparation of azides and alkyl substituents, as well as for transfer reactions such as vinyl ethers. It can also be used to quaternize functional groups and synthesize low molecular weight compounds. DMAP is insensitive to oxygen, making it possible to carry out reactions under air or vacuum. This property also makes DMAP useful in the synthesis of high molecular weight compounds with a high degree of stereoselectivity.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Chloro-4-methoxyphthalazine is a new member of the family of phthalonitriles. It has been shown that this compound is electron rich and can be oxidized to give a radical anion, which can then be used for C-C bond formation. The elimination of chlorine from 1-chloro-4-methoxyphthalazine can take place electrochemically, following the mechanism of the reversible transfer reaction. This chemical property allows 1-chloro-4-methoxyphthalazine to act as an electron source in electrochemical reactions.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,4-Diethoxybenzoic acid is a chemical compound which is found in the essential oil of the plant Dalbergia sissoo. It has been shown to have anti-inflammatory properties and to be a potential therapeutic agent. 2,4-Diethoxybenzoic acid is an acetylated phenolic compound that is used in the production of heartwood extractions. It can act as a mathematical component and can be used in the synthesis of natural products such as isoflavanones. 2,4-Diethoxybenzoic acid has been shown to have antioxidant properties and to inhibit lipid peroxidation at high concentrations.</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>This molecule is a synthetic, physicochemical drug that is used to treat women with metastatic breast cancer. It binds to glutamate receptors and blocks the metabotropic glutamate receptor. Pyrazolo[1,5-a]pyridine has been shown to be effective in clinical trials in treating melanotic lesions. The drug has been shown to have a dose-dependent effect on the central nervous system and can lead to death due to cardiac arrest.</p>

<p>1-Phenylpent-4-yn-1-ol is a ketone that can be synthesized by the desulfonylation of 1,3-dibromopropane. It is a radical that has been shown to have potential in the synthesis of polymers and pharmaceuticals. This compound undergoes sequential desulfonylative coupling with alcohols such as phenylethyl alcohol to produce phenylethylphenol. The use of 1-phenylpent-4-yn-1-ol in this process makes it an environmentally friendly alternative to other more toxic reagents.</p>

<p>Versatile small molecule scaffold</p>

<p>Chroman-3-one is a trifluoroacetate ester that has been shown to have anticancer activity. It is an amine that is used in the synthesis of various drugs and pharmaceuticals. Chroman-3-one is also an important precursor in the manufacture of the antidiabetic drug metformin. The compound is often used in organic synthesis because it can be prepared from readily available starting materials, and it can be easily converted to other compounds using a variety of reactions. Chroman-3-one has two tautomeric forms: one where the carbonyl group is protonated and one where the carbonyl group is deprotonated. This means that it can exist as an enantiopure or a mixture of enantiomers.</p>

<p>2-Methylsulfinylbenzenecarboxylic acid (MSB) is an inorganic compound, which is a ligand in photochromism. It can be used to activate the reaction solution and kinetics of the cyclic voltammetry. MSB has been shown to react with acetonitrile to form sulfoxide, which has absorption spectroscopy that is constant and methanol as solvent. This compound is soluble in solvents such as acetonitrile, dichloromethane, and tetrahydrofuran.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Iodocumene is a chemical that belongs to the group of unsymmetrical carbonyl compounds. It is an intermediate in the synthesis of saccharin and other organic chemicals, as well as in the production of pharmaceuticals. 2-Iodocumene can be used as a ligand in metal-catalyzed cross-coupling reactions between organometallic reagents and various types of electrophiles. This compound has been shown to react with iron at room temperature to form an active catalyst for the regioselective cleavage of C-C bonds. The mechanistic studies have revealed that 2-iodocumene acts as an electron acceptor and a nucleophile, which allows it to act as a bifunctional catalyst during these reactions. The reaction rate depends on steric hindrance, which may be due to the presence of carbonyl groups or cyclic structures. The mechanism is supported by computational studies using density functional</p>

<p>Versatile small molecule scaffold</p>

<p>2,5-Dimethoxybenzenesulfonamide is a piperidine derivative that has been shown to be an efficient electrophile. 2,5-Dimethoxybenzenesulfonamide reacts with protonated metal surfaces, forming a monolayer of high surface area and low coverage. The affinity of this compound for the metal surface is due to its nucleophilic nature. This compound displays a strong adsorption to the metal surface and provides protection from corrosion by acting as an oxygen scavenger. Experimental results have shown that 2,5-dimethoxybenzenesulfonamide exhibits higher efficiencies in the presence of other reactive compounds.<br>2,5-Dimethoxybenzenesulfonamide was used in computational simulations to study the effects of different parameters on the adsorption process. The use of these simulations can provide insight into how changes in experimental conditions affect the efficiency of this molecule.</p>