31558-40-4

Usage

Uses

Used in Pharmaceutical Industry:
4-BROMO-3,5-DIMETHOXYBENZALDEHYDE is used as a key intermediate in the synthesis of various pharmaceutical compounds, including drugs with potential therapeutic applications.
Used in Chemical Synthesis:
4-BROMO-3,5-DIMETHOXYBENZALDEHYDE is used as a chemical building block for the synthesis of more complex organic molecules, such as dyes, fragrances, and other specialty chemicals.
Used in Research and Development:
4-BROMO-3,5-DIMETHOXYBENZALDEHYDE is used as a research compound in the development of new chemical reactions and synthetic pathways, contributing to the advancement of organic chemistry and related fields.

InChI:InChI=1/C9H9BrO3/c1-12-7-3-6(5-11)4-8(13-2)9(7)10/h3-5H,1-2H3

Upstream product

• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 61367-62-2 (4-bromo-3,5-dimethoxyphenyl)methanol 
• 16534-12-6 3,5-dihydroxy-4-bromobenzoic acid 
• 56518-42-4 4-bromo-3,5-dimethoxybenzoic acid 

Downstream Products

• 123796-61-2 2-(4-bromo-3,5-dimethoxyphenyl)-[1,3]dioxolane 
• 31558-32-4 (+/-)-1-(4-bromo-3,5-dimethoxyphenyl)-2-nitropropene 
• 32156-34-6 4-bromo-3,5-dimethoxyphenylisopropylamine 
• 41787-65-9 ancistrocladisine 
• 123796-65-6 1-<4-(2-Aminopropyl)-2,6-dimethoxyphenyl>-4,5-dimethoxy-2-naphthylmethanol 
• 123796-63-4 Methyl 1-(4-Formyl-2,6-dimethoxyphenyl)-4,5-dimethoxynaphthalene-2-carboxylate 
• 123796-68-9 N-<2-<4-(4,5-Dimethoxy-2-methyl-1-naphthyl)-3,5-dimethoxyphenyl>-1-methylethyl>acetamide 
• 123796-67-8 N-<2-<2-(Hydroxymethyl-4,5-dimethoxy-1-naphthyl)-3,5-dimethoxyphenyl>-1-methylethyl>acetamide 
• 134822-51-8 Methyl 1-<2,6-Dimethoxy-4-((E)-2-nitropropenyl)phenyl>-4,5-dimethoxynaphthalene-2-carboxylate 
• 123796-66-7 Acetic acid 1-[4-(2-acetylamino-propyl)-2,6-dimethoxy-phenyl]-4,5-dimethoxy-naphthalen-2-ylmethyl ester 
• 1228308-16-4 C₁₇H₁₇BrO₃ 
• 1268623-66-0 methyl (2E,4E)-7-(4-bromo-3,5-dimethoxyphenyl)-7-((tert-butyldimethylsilyl)oxy)hepta-2,4-dienoate 
• 1268623-54-6 methyl (E)-5-(4-bromo-3,5-dimethoxyphenyl)-5-((tert-butyldimethylsilyl)oxy)pent-2-enoate 
• 344396-19-6 3,5-dimethoxy-4-(1-methylethyl)benzaldehyde 

Relevant academic research and scientific papers

Anti-inflammatory and psoriasis treatment and protein kinase inhibition by hydroxy stilbenes and novel stilbene derivatives and analogues

The present invention provides novel diphenyl ethene compounds and pharmaceutically-acceptable salts thereof. Also provided are methods for making the compounds of the invention as well as methods for the use thereof in the treatment of immune, inflammatory, and auto-immune diseases.

Solid state nuclear bromination with N-bromosuccinimide. Part 2. Experimental and theoretical studies of reactions with some substituted benzaldehydes

N-Bromosuccinimide reacts with aromatic aldehydes in the solid state to yield exclusively nuclear brominated products while a similar reaction in the solution phase produces a number of products under varied conditions. The reactivity and regioselectivity have been studied in terms of the energies of HOMO, HOMO-LUMO difference, reaction free energy, reaction conditions and crystal packing. Single crystal X-ray structural analysis of 3,4-dihydroxybenzaldehyde has been carried out. Crystal packing energies of some of the reactive and unreactive benzaldehydes indicate the importance of molecular bromine diffusion in the solid state.