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

1-Bromo-2-butoxybenzene is a chemical compound that is used in the manufacture of zinc oxide. It is also used as an electrolyte in dye-sensitized solar cells. In these cells, 1-bromo-2-butoxybenzene acts as an electron donor, which provides electrons to the redox dye on the surface of the semiconductor. This process leads to recombination, where electrons and holes recombine to produce electricity. The introduction of alkoxy groups into 1-bromo-2-butoxybenzene molecules allows for increased stability and efficiency in dye-sensitized solar cells.

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

2-[(tert-Butyldimethylsilyl)oxy]benzaldehyde (BBSA) is a traceless synthetic reagent that is used for the termination of peptide synthesis. It can also be used in the synthesis of benzofurans, carbonyl compounds, and thioacetals. The high yield and chemoselectivity makes BBSA a competitive reagent for these types of reactions. BBSA can be prepared from hydrogen peroxide, esters, enol ethers, or peroxides. These latter reactants are more selective than hydrogen peroxide and do not lead to oxidation of substrates or side products. This product is also useful for the synthesis of thioketals.

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

2-Bromo-3,3,3-trifluoro-1-propene is a chemical compound that has been synthesized in an asymmetric reaction. The reactant is bromopropane and the product is 2,2,2-trifluoropropene. The methylene group on the propene molecule is activated by the nucleophilic attack of a fluoride ion from hydrogen fluoride to form a cavity with a highly strained bond. The kinetic study of this reaction revealed that the activation energy for the reaction is 42 kJ/mol. Palladium-catalyzed coupling reactions are catalyzed by palladium and require nonpolar solvents such as toluene or dichloromethane. This type of reaction has been shown to be exothermic with an isolated yield of 1%.

Piperyline is an alkanoic acid that has shown to be effective against skin cancer. It also has antimicrobial properties, which may be due to its ability to bind metal ions and form polymeric compounds. Piperyline inhibits microbial growth by inhibiting the synthesis of proteins and nucleic acids. The antimicrobial activity is related to its cationic polymerization with hydroxyl groups, which forms a structure that can inhibit microbial enzymes and disrupt microbial cell membranes. This compound also interacts with the skin's natural lipids, making it difficult for microorganisms to attach and grow on the skin. Piperyline is synthesized in organic chemistry laboratories as an amide precursor of other pharmaceuticals such as penicillin.