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., COA of Formula: C9H9BrO3.
Banik, Trisha;Kaliappan, Krishna P. research published 《 A Serendipitous One-Pot Cyanation/Hydrolysis/Enamide Formation: Direct Access to 3-Methyleneisoindolin-1-ones》, the research content is summarized as follows. A direct, one-pot conversion of 2′-haloacetophenones 2-X-3-R-4-R1-5-R2C6HC(O)CHR3(R4) (X = Br, I; R = H, azanyl, Ph, etc.; R1 = H, OMe; R2 = H, F, dibenzylaminyl, etc.; R3 = H, Ph, n-Hex, etc.; R4 = H, Me; R1R2 = -OCH2O- and 1-(2-bromopyridin-3-yl)ethanone) to 3-methyleneisoindolin-1-ones I and 5-methylene-5H-pyrrolo[3,4-b]pyridin-7(6H)-one scaffold using CuCN as the sole reagent without the need for moisture-free or anaerobic conditions is reported. This serendipitously discovered transformation with a broad substrate scope provides a significantly different route towards these important scaffolds. The scope of the method has also been further extended towards the synthesis of three special scaffolds, which are analogous to various bio-active drugs.
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., COA of Formula: C9H9BrO3
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary