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>(2-Methoxyphenyl)methanesulfonamide is a linker that contains an amine and a sulfonyl chloride. It is used for solid phase synthesis of amides. This compound can be prepared by reacting amines with acid chlorides in the presence of benzene or chloroform as a solvent. The substituents on the phenyl ring are electron-withdrawing groups, which stabilize the molecule and prevent it from undergoing nucleophilic substitution reactions. (2-Methoxyphenyl)methanesulfonamide reacts with primary amines to form stable amides.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-tert-Butylphenylboronic acid is a versatile and useful reagent that is used in organic synthesis for the preparation of chiral boronates. This compound has been shown to form complexes with many different metal ions and can be used to synthesize supramolecular structures. Studies have shown that 2-tert-butylphenylboronic acid reacts with diastereomeric biphenyls in the presence of a base to form a complex that can be separated into its two diastereomers by crystallization, affording two different products.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-methoxycyclohexan-1-ol is a dipole with the monosubstituted, monomeric structure. It is an isomer of cyclohexanol and can be found as a mixture of two conformers, cis and trans. The molecule has hydrogen bonds between the OH group on C3 and the O atom on C4. 3-methoxycyclohexan-1-ol has been shown to be stabilized by hydrogen bonding to chlorine. The molecule also has intramolecular hydrogen bonding in the form of a bond cleavage. 3-methoxycyclohexan-1-ol has a molecular weight of 114.14 g/mol and its nmr spectrum displays signals in both d and t time domains due to its conformational 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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Chloro-4-methoxybenzene-1-thiol is a chlorinated aromatic compound that is used as an intermediate in the synthesis of sulphones. It is prepared by the reaction of aluminium with hydrochloric acid, then followed by the addition of sulphur chloride. The product precipitates as a yellow solid and has a melting point of about 40°C. 3-Chloro-4-methoxybenzene-1-thiol does not react with water or dilute acids, but reacts with alkalis to form salts.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-(2-Methylpropoxy)propan-1-ol is a volatile organic chemical that can be used as a solvent in the production of paints and coatings. It is also used as an intermediate in the manufacture of other chemicals, such as trichloroethane and ethylene dichloride. 3-(2-Methylpropoxy)propan-1-ol has been detected by gas chromatography using a flame ionization detector (GC/FID) in oleoresin samples from oranges and pineapples. Recoveries of 3-(2-methylpropoxy)propan-1-ol from orange oleoresin were found to be 87%.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5,5,5-Trifluoropentanonitrile is a heterocyclic compound that can be used as an intermediate in the synthesis of other chemicals. It is a versatile chemical that has been successful in the discovery and development of new drugs for use as anti-inflammatory or anti-cancer agents. 5,5,5-Trifluoropentanonitrile is also useful for the production of ketones and functional groups.</p>

<p>2-(Hydroxyamino)-2-oxoethylphosphonic acid is an inhibitor of the enzyme senescent and is used to treat cancer. It inhibits the enzymatic reaction of the enzyme by binding to a hydrogen bond in the active site, thereby preventing its function. The compound has been shown to inhibit tumor growth in vitro and in vivo models. 2-(Hydroxyamino)-2-oxoethylphosphonic acid is also used for diagnostic purposes, as it can be detected in urine samples. This inhibitor binds to a water molecule that reacts with the phosphate group on the phosphonate backbone, which prevents it from binding to other phosphate groups on other molecules. This inhibition leads to a decrease in ATP production, which is essential for cell division.</p>

<p>Methyl 2,3-dihydro-1H-indole-1-carboxylate (MDIC) is a nitro compound that is used as an ingredient in pharmaceutical preparations. It is a non-selective competitive inhibitor of the enzyme active oxygen species and has been shown to have reactive effects on amines and carboxylic acids. MDIC also inhibits the production of active oxygen species by reacting with heterocycles, such as tetrahydropyran, heterocycloalkyls, or amines. This chemical has shown activity against osteopathic, porcine, and other animal models of inflammation. MDIC also reacts with heme, which can inhibit the formation of free radicals that play a role in inflammation.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Chloro-5-cyanobenzoic acid is a sclerotinia inhibitor that is used in the chemical synthesis of benzamide. It has been shown to inhibit the growth rate of sclerotinia by binding to the mycelium, spores, and other structures with methyl esters. The compound has also been shown to be magnetic and have a high hydrogen spectrum. 2-Chloro-5-cyanobenzoic acid can be synthesized from hydroxylamine and benzoyl chloride in the presence of cuprous cyanide. This chemical has also been shown to be effective at inhibiting sclerotinia growth on cotton plants.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-(2-Bromoethyl)cyclopentan-1-one is a synthetic compound that belongs to the class of bicyclic proline analogues. It can be synthesized by cyclization of an ester with a bromocyclopentane. This reaction can be accomplished using acid or base catalysis, and it leads to the formation of a six-membered ring with two chiral centers. The enantiopure form (enantiomerically pure) has been isolated in moderate yield from racemic mixtures by enantiopyrase resolution. This synthetic compound has shown promising results as an anticonvulsant, although its therapeutic potential is not yet fully understood.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>The synthesis of 1-iodo-3-methylcyclohexane is reported. In this method, chloroamine reacts with transmetallation to form a terminal alkynyl halide. The terminal alkyne can be converted to an iodide by reaction with sodium iodide and then reacted with cyclohexene to produce the desired product. This synthesis is achieved by using a chiral ligand. The reaction mechanism for this process has been determined to be a concerted β-elimination followed by transmetallation.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-(Propan-2-yl)pyrrolidin-2-one is an eluting enantiomer of phenylcarbamate. This compound has been shown to have antimicrobial activity and inhibit the growth of bacteria in culture. 4-(Propan-2-yl)pyrrolidin-2-one is soluble in ethanol and ethyl acetate, but insoluble in water, n-hexane, and tertiary butanol.</p>

<p>Methyl Piperidine-3-carboxylate Hydrochloride is a nucleophilic compound that can be synthesized by condensation of benzylamine and methyl piperidin-3-carboxylate. This reaction takes place in the presence of strong acid, such as sulfuric acid, or in the presence of an organic base, such as potassium hydroxide. The intramolecular condensation reaction proceeds through a six-membered ring intermediate. The final product is formed by dehydration and thiohydantoin formation. Methyl Piperidine-3-carboxylate Hydrochloride has been shown to have antihypertensive effects in rats. It also has anticonvulsant properties and can be used to treat epilepsy in humans.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>