Building Blocks

<p>3-Chloro-1-methyl-1H-pyrazole is a regioselective, heterocyclic compound. It is a halovinyl derivative of pyrazole and is used in the synthesis of other heterocycles. 3-Chloro-1-methyl-1H-pyrazole has been found to be an efficient synthetic intermediate for both ketones and pyrazoles. The reaction mechanism for this compound involves an initial alkylation followed by a substitution reaction with the nucleophilic hydroxyl group. The final product is formed via a heterocyclization step involving fragmentation and halogenation.</p>

<p>1-Cbz-2-methylpyrrolidine-2-carboxylic acid is an orally active PARP inhibitor that has been shown to inhibit tumor growth in clinical trials. It is a carboxamide derivative with a cyclic structure. 1-Cbz-2-methylpyrrolidine-2-carboxylic acid blocks cellular proliferation and induces apoptosis by inhibiting DNA synthesis and protein expression. This agent also inhibits the growth of murine melanoma cells in vitro, as well as xenografts in vivo. In addition, 1-Cbz-2-methylpyrrolidine-2-carboxylic acid has been shown to be more potent against cancer cells than other PARP inhibitors, such as abt 888.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl 4-aminobenzoate hydrochloride is a compound that is soluble in water and has a molecular weight of 155.14 g/mol. The compound has an acidic nature, with the pKa being 2.5, which makes it a proton donor and an acid catalyst. It can be used to synthesize retinoic acid, which is used to treat acne, by reacting with glycinamide ribonucleotide. Methyl 4-aminobenzoate hydrochloride can also be used for sample pretreatment before analysis by gas chromatography (GC), liquid chromatography (LC) or mass spectrometry (MS). This compound is not highly polar and can therefore be dissolved in non-polar solvents such as hexane or dichloromethane. Methyl 4-aminobenzoate hydrochloride reacts with anthracene and amines to form methyl derivatives.</p>

<p>Versatile small molecule scaffold</p>

<p>1-Iodo-4-methoxy-2-methylbenzene (1IMMB) is an iodide which has been used as a precursor in the synthesis of carbonyl groups. This compound has also been shown to have high yields and mechanistic. The carbonyl group is located at the 1,3 positions and the methoxy group is located at the 2 position. This compound reacts with acetonitrile to form a naphthalene derivative. 1IMMB also reacts with an alcohol to form a cyclic ether with regiospecificity. It can also be used as a catalyst in the synthesis of unsymmetrical compounds that contain both carbonyl groups and alcohols.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-(2-Ethylhexyl) 4-methyl benzene-1,4-dicarboxylate is a silylated, polysulphide sealant with good adhesion to many plastics and metals. It is also used as a plasticizer for acrylates and a sealant for polyurethanes. This product has been shown to be an effective sealant for terephthalate and polyethers. The molecule contains two ester groups that react with the hydroxyl groups on the surface of the substrate to form the crosslinked network.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>8-Chloro-1H-benzo[D][1,3]oxazine-2,4-dione is an organic chemical used as a precursor to pharmaceuticals. It is produced by the esterification of an acid chloride with a carboxylic acid. This chemical can be converted into other products through hydrogenation or hydrochlorination. 8-Chloro-1H-benzo[D][1,3]oxazine-2,4-dione is also used in the production of xylene and dichlorobenzene. This compound has two isomers that differ in their reactivity due to steric hindrance. The less reactive isomer has been shown to have antiinflammatory effects in mice.</p>

<p>Cyclobutane-1,3-diol is an organic compound that is a viscous liquid at room temperature. It is used in the production of polyesters and coatings. Cyclobutane-1,3-diol has been shown to be a good ligation partner with ethylene glycol in the liquid phase. It also has been used as an impurity scavenger and as a skeleton for other compounds. Cyclobutane-1,3-diol can be purified by distillation or crystallization, but it may contain fluorine or alkali metal residues that are difficult to remove. There are two stereoisomers of cyclobutane-1,3-diol: D-(+)-cyclobutane-1,3-diol and L-(+)-cyclobutane-1,3-diol.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-(4-Nitrophenyl)-5-phenyl-1H-pyrazole is a dipole tautomeric proton tautomer with a fluorescence photophysical. It has a molecular orbital that is acidic. 3-(4-Nitrophenyl)-5-phenyl-1H-pyrazole has the following transfer functional groups: nitro, fluorescence, and photophysical. 3-(4-Nitrophenyl)-5-phenyl-1H-pyrazole is an experimentally determined molecule with a molecular orbitals of acidic. It has two tautomers, which are the dipole and tautomers. The dipole tautomeric proton tautomer is the more stable form of 3-(4-Nitrophenyl)-5-phenyl-1H-pyrazole in solution.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>