1001590-53-9

Upstream product

• 4521-61-3 3,4,5-Trimethoxybenzoyl chloride 
• 909724-13-6 dithiocarbonic acid O-ethyl ester S-[2-oxo-2-(3,4,5-trimethoxyphenyl)-ethyl] ester 
• 1036271-71-2 (Z)-3-chloro-3-(thiophen-2-yl)acrylaldehyde 
• 1001590-50-6 2-bromo-5-(3,4,5-trimethoxybenzoyl)thiophene 
• 54663-78-4 tributyl(thien-2-yl)stannane 

Downstream Products

• 1001590-54-0 5-bromo-5'-(3,4,5-trimethoxybenzoyl)[2,2']bithiophene 
• 1001590-58-4 5-bromo-5'-(3,4,5-tri-n-octadecyloxybenzoyl)-[2,2']bithiophene 
• 1001590-57-3 5-bromo-5'-(3,4,5-tri-n-tetradecyloxybenzoyl)-[2,2']bithiophene 
• 1001590-56-2 5-bromo-5'-(3,4,5-tri-n-dodecyloxybenzoyl)-[2,2']bithiophene 
• 1001590-55-1 5-bromo-5'-(3,4,5-trihydroxybenzoyl)-[2,2']bithiophene 

Relevant academic research and scientific papers

Design, synthesis, and biological evaluation of thiophene analogues of chalcones

Chalcones are characterized by possessing an enone moiety between two aromatic rings. A series of chalcone-like agents, in which the double bond of the enone system is embedded within a thiophene ring, were synthesized and evaluated for antiproliferative

Columnar liquid crystalline π-conjugated oligothiophenes

Polycatenar oligothiophenes possessing three alkoxy chains at each terminal self-organise into columnar liquid crystalline phases, and one-dimensional columnar stacks can be oriented uniaxially by mechanical shearing in the mesophases. The Royal Society o