Ramesh, Golla team published research in Journal of Organic Chemistry in 2022 | 5392-10-9

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., Reference of 5392-10-9

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. Reference of 5392-10-9.

Ramesh, Golla;Ramulu, Bokka Venkat;Balamurugan, Rengarajan research published 《 Activation of o-Propargyl Alcohol Benzaldehydes under Acetalization Conditions for Intramolecular Electrophile Intercepted Meyer-Schuster Rearrangement》, the research content is summarized as follows. The reactivity of o-propargyl alc.-containing benzaldehydes I [R1 = H, 5-O2N, 5-MeO, 4,5-(MeO)2; R2 = R3 = Me, Ph; R2 = H, R3 = Ph, 4-MeC6H4, 1,3-benzodioxol-5-yl, etc.; R2 = Me, R3 = Ph, 4-ClC6H4, 2-naphthyl, etc.; R2 = Ph, R3 = 4-BrC6H4, 4-ClC6H4, 4-MeC6H4] has been increased tremendously toward Bronsted acid-catalyzed intramol. electrophile-intercepted Meyer-Schuster (M-S) rearrangement under acetalization conditions using tri-Me orthoformate. The in situ formed acetal transfers the methoxy group intramolecularly to generate the M-S intermediate in even less reactive substrates, and the formed oxocarbenium ion makes the carbonyl more electrophilic for an effective intramol. trapping of the M-S intermediate to furnish the indanone derivatives II. This procedure was applied to propargyl alc.-functionalized cycloalkenecarboxaldehydes to afford the corresponding cycloalkane-fused (alkylidene)(methoxy)cyclopentenones.

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., Reference of 5392-10-9

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary