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., Application In Synthesis of 5392-10-9.
Li, Xin;He, Songtao;Song, Qiuling research published 《 Rapid incorporation of a difluoroacetate radical into para-quinone methides via radical 1,6-conjugate addition》, the research content is summarized as follows. A simple but efficient protocol to rapidly incorporate difluoroacetate radical into para-quinone methides I (R = 4-methoxyphenyl, thiophen-2-yl, Me, etc.; R1 = t-Bu, i-Pr, Me; R2 = t-Bu, i-Pr) through dialkylzincs induced radical 1,6-conjugate addition pathway. Besides achieving high yields and excellent functional group compatibility, this protocol allowed the incorporation of a gem-difluoromethylene motif to be accomplished within minutes.
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