Building Blocks

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Dimethylphosphorylbenzene is an inorganic compound that is a phosphine, a class of organometallic compounds. It has been shown to have a catalytic effect on the reaction between acyl halides and carbon disulphide. Dimethylphosphorylbenzene has also been studied for its use as a polymerization initiator in lithography. Its light-emitting properties are due to the presence of a hydroxyl group and its ability to undergo photochemical reactions following exposure to light.

Versatile small molecule scaffold

8-(Tosylamino)quinoline is a quinoline derivative that inhibits the production of tumor necrosis factor-α (TNF-α) and other inflammatory mediators. 8-(Tosylamino)quinoline has been shown to inhibit the proliferation of muscle cells, which may be due to its anti-inflammatory properties. This drug also suppresses genes that are involved in cell growth and signaling, such as suppressor genes. 8-(Tosylamino)quinoline binds copper ions, which prevents the formation of reactive oxygen species and blocks the activation of nuclear factor kappa beta (NFκB), which regulates immune responses. It also inhibits autophagy, a process by which cells destroy their own intracellular contents during periods of starvation or stress.

2-(Cyclohexylamino)benzoic acid is a chemical compound that reacts with aryl halides to form cyclic amines. The reaction proceeds by the formation of an intermediate, which is then hydrolyzed and decarboxylated to form the product. This reaction can be used for the synthesis of amines from either aromatic or aliphatic aryl chlorides. This process is often used in screening experiments because it has been shown to be selective for aryl halides and yields high yields. The addition of cross-coupling reactions can also yield high yields and produce desired products with good chemo- and regioselectivity. 2-(Cyclohexylamino)benzoic acid is also useful for the synthesis of hyperpolarized molecules for imaging studies, as well as in ultrafast experiments where transfer rates are important.

Isophorone Oxide is a molecule that contains a carbonyl group. It is unreactive and does not form hydrogen bonds or react with hydroxy groups. Isophorone oxide has two reactive groups, the hydroxyl group and amido group, which are responsible for its chemical properties. The electron reduction of the carbonyl group can be achieved by using deionized water as a reducing agent. In solution form, Isophorone Oxide is colorless to light yellow liquid with a molecular weight of 144.16 g/mol.

Versatile small molecule scaffold

N-Butylbutanamide is a colorless, volatile liquid that has a distinctive odor. It is used as an intermediate in the production of other chemicals and a solvent for coatings and adhesives. N-Butylbutanamide has been shown to react with amines and amides with high concentrations of primary alcohols to form diazirine. Diazirine can be detected by UV spectroscopy at 254 nm and by mass spectrometry. N-Butylbutanamide can be analyzed using on-line liquid chromatography or GCMS.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Diethyl Isobutylmalonate is a solid catalyst that is used in the organic synthesis of ester compounds. This compound is an organometallic compound with a diethyl group bound to an iso-butyl group and malonic acid. The active methylene group of this molecule reacts with carboxylic acids, such as picolinic acid, to form esters. Diethyl Isobutylmalonate can be used with an acid catalyst to cross-link peptides. The hydroxyl group on the molecule can react with amine groups on proteins and also bind to aromatic hydrocarbons.

1-Methyl-4-phenyl-1H-pyrazole is a regiospecific cross-coupling agent that reacts with alkenes to form pyrazoles. It is typically used in palladium-catalyzed cross-coupling reactions for the synthesis of 1,2,3-triazoles. Pyrazoles are also found as natural products in plants and animals and have been shown to be effective as anti-cancer drugs and against chronic viral infections. They are also involved in iron binding and have been shown to inhibit the activity of isomerases such as glucose 6 phosphate isomerase. 1Methyl-4-phenyl-1H-pyrazole is commercially available, but can be synthesized by reacting benzonitrile with styrene followed by allylation with ethylene or propylene oxide. The compound has been optimized for photocleavage, which makes it useful for generating azadiene derivatives.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold