A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. 5392-10-9, formula is C9H9BrO3, Name is 2-Bromo-4,5-dimethoxybenzaldehyde. Organobromine compounds have fallen under increased scrutiny for their environmental impact., Computed Properties of 5392-10-9.
Xu, Xianjun;Song, Liangliang;Feng, Huangdi;Van der Eycken, Erik V. research published 《 Direct Access to 4-Substituted Isoquinolones via a Sequential Pd-Catalyzed Cyclization/Base-Promoted Aromatization/Ring-Opening of N-Propargyl-1,3-oxazolidines》, the research content is summarized as follows. Herein, a practical Pd-catalyzed cyclization/base-promoted aromatization/ring-opening protocol of N-propargyl-1,3-oxazolidines with carboxylic acids was disclosed. In the current domino reaction, a series of ester-functionalized isoquinolones I [R1 = Ph, 4-MeC6H4, 2-FC6H4, etc.; R2 = H, 6-Me, 7-MeO, etc.; R3 = Ph, 4-MeC6H4, 4-ClC6H4; R4 = Me, t-Bu, Ph, etc.] was obtained in moderate to good yields via C-O bond cleavage, which features a broad functional group tolerance.
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., Computed Properties of 5392-10-9
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary