73877-29-9

Upstream product

• 73877-35-7 1-(7-bromo-6-hydroxy-4-methoxy benzofuran-5-yl)ethanone 
• 123-11-5 4-methoxy-benzaldehyde 
• 82-57-5 visnagin 
• 96583-74-3 9-bromo-4-methoxy-7-methyl-5H-furo[3,2-g]chromen-5-one 

Downstream Products

• 1616883-61-4 9-bromo-4-methoxy-7-(4-methoxyphenyl)-5H-furo[3,2-g]chromen-5-one 

Relevant academic research and scientific papers

Design, synthesis and structure-activity relationship of novel semi-synthetic flavonoids as antiproliferative agents

Various flavonoid scaffold based derivatives viz furochalcones (3a-e, 6a-d and 9a-d), furoflavones (10a-d, 11a-d, 12a-d, 18a&b), flavones (21a-d), furoaurones (13a,b, 14a-d and 15a-d) and 7-styrylfurochromones (22a-d and 25a-e) were designed and synthesiz

DNA binding, antiviral activities and cytotoxicity of new furochromone and benzofuran derivatives

Bromination of visnagin (1) afforded 9-bromovisnagin (2) which on its alkaline hydrolysis afforded the 3-acetyl benzofuran derivative (3). The condensation of (3) with hydrazine hydrate, phenylhydrazine and/or hydroxylamine hydrochloride afforded the corr