Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Phenylglutaric anhydride is a chemical compound that is used in organic chemistry as a phase-transfer reagent, because of its ability to exchange between the organic and aqueous phases. It has been shown to be a useful modifier for preparative high performance liquid chromatography (prep HPLC) due to its low solubility in water and non-volatility. 2-Phenylglutaric anhydride can be used as a sample preparation technique for the separation of carboxylic acid derivatives by preparative HPLC. The use of this chemical has allowed for advances in the field of preparative chromatography, including the development of new strategies and techniques.<br>2-Phenylglutaric anhydride is also known to have thermodynamic properties that are favorable for column chromatography. This compound has been shown to be stable at higher temperatures, which allows for optimization of column packing materials with supercritical fluids.</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>Dimethyl (methylsulfanyl)(sulfanylidene)phosphonite is an organophosphorus insecticide. It inhibits the cytochrome P-450 enzymes, which are involved in the synthesis of various compounds. Dimethyl (methylsulfanyl)(sulfanylidene)phosphonite is a toxicant for animals and can cause lung toxicity. The toxicity of dimethyl (methylsulfanyl)(sulfanylidene)phosphonite depends on its impurities, such as 7-ethoxycoumarin. The metabolism of dimethyl (methylsulfanyl)(sulfanylidene)phosphonite in humans has been studied using liver microsomes from different species and tissues. One study found that cytochrome P-450 isoenzymes CYP2B1 and CYP2C11 were involved in the detoxification of this compound. Another study found that phosalone was an intermediate metabolite that was formed by</p>

<p>Versatile small molecule scaffold</p>

<p>3-(Bromomethyl)-3-ethyloxetane is a monomer that can be used to make copolymers. It has been shown to have good thermal stability and the ability to be polymerized with other oxetanes. 3-(Bromomethyl)-3-ethyloxetane has also been shown to form copolymers when mixed with other oxetanes. The type of copolymer formed depends on the combination of other oxetanes and their ratios. 3-(Bromomethyl)-3-ethyloxetane can be used for x-ray diffraction analysis, which can help determine the structure of the polymer and its properties.</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-(2-Hydroxypropan-2-yl)phenol is a petrochemical that is obtained from the hydrolysis of phenol. It can be used as a stabilizer for polymers and has been shown to selectively stabilize polystyrene and polypropylene. 4-(2-Hydroxypropan-2-yl)phenol also helps in the crystallization of intermediates, such as 2,4,6-trihydroxyphenylacetic acid, which are used in organic synthesis. The high yield of this chemical makes it an efficient and cost-effective process. 4-(2-Hydroxypropan-2-yl)phenol is also useful in the conversion of phenols into adducts with polymers, which can be used in plastics manufacturing.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-(4-Acetylbenzenesulfonyl)piperidine-4-carboxylic acid is a chemical compound that belongs to the group of piperidines. It has been shown to interact with proteins in cell biology, pharmacology, and research tools. 1-(4-Acetylbenzenesulfonyl)piperidine-4-carboxylic acid has been shown to inhibit the activity of ion channels and can be used as a tool for research on these channels. It also interacts with antibodies, peptides, and ligands, as well as receptors and ion channels.</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>1,3-Dihydrospiro[indene-2,2'-pyrrolidine] is a chiral dopaminergic compound that has been shown to have analgesic and antipsychotic properties. It has also been shown to be a dopamine agonist and to have antagonist properties. This drug interacts with the dopaminergic system in the brain by blocking the reuptake of dopamine and increasing its levels in the synapse. It is likely that 1,3-dihydrospiro[indene-2,2'-pyrrolidine] would be used as an analgesic or antipsychotic medication.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-(Aminomethyl)pyridin-2-amine (5-APA) is a chemical compound with the molecular formula CHClN. 5-APA is an organic base that can be used as a solvent, such as in the extraction of metals and other compounds. It is also used to make other chemicals, including pharmaceuticals, solvents, and dyes. 5-APA is soluble in water and reacts with acids to form hydrogen chloride gas and ammonia gas. The product can evaporate when heated. The boiling point of 5-APA is -13°C and its melting point is -1°C. Its density at 20°C is 1.6 g/mL and it has a specific gravity of 1.856 at 20°C. 5-APA has a vapor pressure of 7 mm Hg at 25°C. It has a diameter of 0.906 cm at 25°C and a flow rate of</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Pyrazolo[1,5-a]pyridin-5-ol is a volatile compound that is extracted from the headspace of solid phase microextraction. It has been shown to be present in insects and fungi and has been identified as one of the major volatiles in the aroma of hexanal and tetramethylpyrazine. Pyrazolo[1,5-a]pyridin-5-ol is a precursor to pyridine and derivatives. It has also been shown to inhibit the growth of Aspergillus niger and Penicillium bimaculatus through its antimicrobial activity.</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-(Difluoromethyl)-4H-chromen-4-one is an organic compound that is a member of the class of compounds known as oximes. It reacts with hydroxylamine to form a cyclic amine and a dioxime. 2-(Difluoromethyl)-4H-chromen-4-one can be used in the synthesis of a number of biologically active compounds. For example, it was used in the cyclodehydration reaction to synthesize 3,3′,5,5′-tetrahydroxybenzoin. The reactivity of this compound has been studied extensively using spectroscopy and X-ray crystallography.</p>

<p>6-Methyl-1,3-benzothiazole is a chemical compound that belongs to the class of sulfur. It has been patented for use in the treatment of hepatitis C. 6-Methyl-1,3-benzothiazole is a substituent that can be found in pharmaceutical chemicals. The chemical formula for this compound is C6H4S.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-Methoxy-1,3-benzothiazole is a cyclic heterocycle that has an optical yield of 2.5%. It is soluble in nonpolar solvents and has a reactive nature. The compound can be used to create benzothiazoles, styryl dyes, and other heterocycles. 5-Methoxy-1,3-benzothiazole is also used as a reagent to make quinazolinones and nonionic surfactants. The compound's optical properties are affected by the methylene group, which can be substituted with other groups to alter the properties of the molecule.</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-Aminoethyl)sulfanyl]sulfonic acid is an inorganic compound and a corrosion inhibitor. It is the ammonium salt of sulfonic acid, with a pK of 3.75. The molecule has two nitrogen atoms and one sulfur atom, which are unreactive with other compounds and do not form bonds. It is soluble in water, alcohols, ethers, chloroform, and carbon tetrachloride. [(2-Aminoethyl)sulfanyl]sulfonic acid can be used as a corrosion inhibitor for metals such as iron or copper because it does not corrode the metal like some other substances containing sulfur or nitrogen would. This compound also has an acidic nature because it can act as a proton donor to cleave bonds that are second-order rate constants. [(2-Aminoethyl)sulfanyl]sulfonic acid also reacts with aziridine in simulated gas phase reactions to form sulf</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Hydroxy-2,3,5-trifluorobenzoic acid is a compound that contains fluorine and it belongs to the group of organometallic compounds. It is a crystalline substance with an isomeric structure. 4-Hydroxy-2,3,5-trifluorobenzoic acid has been used as a model compound for studies on organic synthesis and hydrolysis reactions. It can also be used as an intermediate in the manufacture of other organic compounds. The use of 4-hydroxy-2,3,5-trifluorobenzoic acid in organic synthesis provides a convenient route to 2,3,4,5-tetrafluorobenzoic acid.</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-[2-(Trimethylsilyl)ethynyl]-phenol is an alkyne that can be used in coupling reactions to form terminal alkynes. The compound is also a precursor to azobenzene and aryl iodides, which are useful in chemical synthesis. 2-[2-(Trimethylsilyl)ethynyl]phenol can be isolated from the reaction of 3-iodo-1-propyn-1-ol with ethyne. The yield of this reaction is usually low because it is difficult to isolate the product from other byproducts.</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>