AC-39094 - bis4-bromophenylacetylene-97 | 2789-89-1

2-Bromophenylacetylene

3-Bromophenylacetylene

4-Bromophenylacetylene is a molecule that can be activated by nucleophilic attack, which is the process of reacting with a nucleophile. It is used in clinical studies to determine the activity of pancreatic lipase in humans and animals. 4-Bromophenylacetylene has been shown to have a high degree of regiospecificity, meaning that it only reacts with certain carbon atoms on the molecule, and not all of them. This allows for selective reactions to take place. 4-Bromophenylacetylene also reacts with amines, which are organic molecules containing nitrogen and hydrogen, through an X-ray absorption process. X-ray absorption is defined as an x-ray photon being absorbed by an electron in a molecule, causing the electron to change its energy level and state. The energy level and state changes are characterized by x-ray emission spectroscopy (XES).

2-Bromophenylacetylene is a synthetic chemical that has been shown to have cytotoxic activity in cervical cancer cells. It was also found to be luminescent, with an emission peak at 535 nm and a maximum quantum yield of 0.3%. 2-Bromophenylacetylene is an adsorbent for sulfonic acid and chloride ions, which can be used for the detection of these ions in water samples. This compound also reacts with lysine residues on histones H3 and H4, which may play a role in its cytotoxic activity. 2-Bromophenylacetylene contains a carbonyl group that can react with the amine group on histone H3 or H4, forming an imine bond. The imine bond can then react with hydroxyl groups on other proteins, leading to cross-linking of the proteins and subsequent cell death.

3-Bromophenylacetylene is a metastable compound that is used in the synthesis of alpha-synuclein. This compound can be synthesized by the hydroboration of phenylacetic acid followed by the oxidation of the boronic ester with sodium hypochlorite. 3-Bromophenylacetylene has been shown to act as a ligand for copper and palladium, which enables it to be used in cross-coupling reactions. In addition, this compound can be used for light emission, due to its ability to undergo hydrosilylation.