90841-64-8

Usage

Uses

Used in Pharmaceutical Research:
1-(4-bromo-2,5-dimethoxyphenyl)ethanone is used as an intermediate in pharmaceutical research for the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a key component in the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(4-bromo-2,5-dimethoxyphenyl)ethanone is used as a building block for the production of other organic compounds. Its versatile structure makes it a valuable precursor in the synthesis of specialty chemicals with specific properties and applications.
Used in Drug Development:
1-(4-bromo-2,5-dimethoxyphenyl)ethanone has potential applications in the development of new drugs. Its chemical properties and structure can be utilized to create novel pharmaceuticals with improved efficacy, safety, and selectivity for various therapeutic targets.
Used in Chemical Industry:
In the chemical industry, 1-(4-bromo-2,5-dimethoxyphenyl)ethanone can be employed as a raw material or intermediate in the synthesis of specialty chemicals. Its unique structure and reactivity make it suitable for the production of various chemical products with specific applications in different industries.

Upstream product

• 25245-34-5 1-bromo-2,5-dimethoxybenzene 
• 75-36-5 acetyl chloride 

Downstream Products

• 120128-75-8 2-(4-bromo-2,5-dimethoxyphenyl)-2-methyl-1,3-dioxolane 
• 807631-08-9 2,5-dimethoxy-4-bromo-α-bromoacetophenone 
• 677277-62-2 2-amino-1-(4-bromo-2,5-dimethoxy-phenyl)-ethanol 
• 807631-06-7 (+/-)-2-(4-bromo-2,5-dimethoxyphenyl)morpholin-5-one 
• 807631-16-9 1-hydroxy-1-(4-bromo-2,5-dimethoxyphenyl)-2-(chloroacetylamino)ethane 
• 88278-14-2 trans-2-(2,5-dibenzyloxy-4-bromophenyl)-6-methoxy-2-methyl-6H-pyran-3(2H)-one 
• 88278-14-2 cis-2-(2,5-dibenzyloxy-4-bromophenyl)-6-methoxy-2-methyl-6H-pyran-3(2H)-one 
• 120128-73-6 Acetic acid (1S,9S,10R,11R,12R)-4,12-bis-benzyloxy-5-bromo-11-iodo-1-methyl-8,13-dioxa-tricyclo[7.3.1.0^2,7]trideca-2,4,6-trien-10-yl ester 
• 120128-72-5 (1S,9S,10R,11S,12R)-4,12-Bis-benzyloxy-5-bromo-11-iodo-1-methyl-8,13-dioxa-tricyclo[7.3.1.0^2,7]trideca-2,4,6-trien-10-ol 
• 120128-71-4 C₂₆H₂₃BrO₅ 
• 88278-12-0 2-(2,5-dibenzyloxy-4-bromophenyl)-6-hydroxy-2-methyl-6H-pyran-3(2H)-one 
• 88278-21-1 C₁₉H₁₅BrO₅ 
• 120147-77-5 C₁₉H₁₇BrO₅ 
• 88278-20-0 8-benzyloxy-9-bromo-6-methyl-2,6-epoxy-6H-1-benzoxec-3-en-5(2H)-one 

Relevant academic research and scientific papers

SYNTHESIS OF THE C-GLYCOSIDE FRAGMENT OF NOGALAMYCIN AND SOME NOGALAMYCIN PRECURSORS

A short, stereoselective method for generation of the fused C-glycoside unit of the anticancer agent nogalamycin is described; in particular, synthesis of the D,E,F ring system.The method utilises a total synthesis of the glycosidic unit from an aryl fury