Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 5392-10-9, formula is C9H9BrO3, Name is 2-Bromo-4,5-dimethoxybenzaldehyde. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. Application In Synthesis of 5392-10-9.
Camilo, Nilton S.;Santos, Hugo;Zeoly, Lucas A.;Fernandes, Fabio S.;Rodrigues, Manoel T. Jr.;Silva, Thiago S.;Lima, Samia R.;Serafim, Jose Claudio;de Oliveira, Aline S. B.;Carpanez, Arthur G.;Amarante, Giovanni W.;Coelho, Fernando research published 《 An Improved Protocol for the Morita-Baylis-Hillman Reaction Allows Unprecedented Broad Synthetic Scope》, the research content is summarized as follows. The effects of several Broensted acids on the rate of DABCO-catalyzed MBH reactions were evaluated. The protocol was operationally simple, involving neat and open-flask conditions and was compatible with a wide range of reagents. A general acid catalysis mechanism was suggested to be responsible for the rate increase. The synthetic versatility of the MBH adducts was exemplified with a two-steps diastereoselective synthesis of the natural product (±)-sitophilure. This acid-mediated protocol can be potentially used as a general methodol. for the MBH reaction.
5392-10-9, 2-Bromo-4,5-dimethoxybenzaldehyde is a useful research compound. Its molecular formula is C9H9BrO3 and its molecular weight is 245.07 g/mol. The purity is usually 95%.
2-Bromo-4,5-dimethoxybenzaldehyde is a synthetic compound that has been shown to be an effective agent for inducing apoptosis in leukemia cells. It is an efficient method for synthesizing the compound and ha2-Bromo-4,5-dimethoxybenzaldehyde induces cell death by topoisomerase-mediated DNA cleavage, which results in chromosomal fragmentation and high levels of reactive oxygen species in the cell., Application In Synthesis of 5392-10-9
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary