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., Related Products of 5392-10-9.
Xie, Fukai;Zhang, Bo;Chen, Yanyu;Jia, Hongwei;Sun, Lei;Zhuang, Kaitong;Yin, Lili;Cheng, Maosheng;Lin, Bin;Liu, Yongxiang research published 《 A Gold(I)-Catalyzed Tandem Cyclization to Benzo[b]indeno[1,2-e][1,4]diazepines from o-Phenylenediamines and Ynones》, the research content is summarized as follows. A gold-catalyzed tandem cyclization of o-phenylenediamines 2-(NH2)-4,5-(R)2C6H2NH2 (R = H, Me, F, Cl, Br) with ynones 2-(CH(OCH3)2)-4-R2-5-R3C6H2CCC(O)R1 (R1 = Ph, naphthalen-2-yl, thiophen-2-yl, etc.; R2 = H, F, Cl, OMe; R3 = H, F, Cl, Me, OMe; R2R3 = -OCH2O-) to synthesize benzo[b]indeno[1,2-e][1,4]diazepines I has been developed. The mechanism was explored by control experiments The method provides a way to access a range of benzo[b]indeno[1,2-e][1,4]diazepine derivatives I in diversity-oriented synthesis aiming at discovering structurally diverse scaffolds.
Related Products of 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., 5392-10-9.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary