905751-80-6

Upstream product

• 103275-75-8 2-isopropoxy-3-methoxyphenol 
• 75792-35-7 2-isopropoxy-3-methoxy-benzaldehyde 

Downstream Products

• 945772-48-5 2-t-butyldimethylsilyl-3-(3,5-dimethoxybenzoyl)-7-isopropoxy-6-methoxy-benzo[b]furan 
• 905752-33-2 2-t-butyldimethylsilyl-7-isopropoxy-6-methoxy-3-(3,4,5-trimethoxybenzoyl)-benzo[b]furan 
• 1007198-30-2 C₂₅H₃₂O₇Si 
• 905752-39-8 7-O-acyl-2-(t-butyldimethylsilyl)-6-methoxy-3-(3,4,5-trimethoxybenzoyl)-benzo[b]furan 
• 905752-30-9 7-O-acyl-2-bromo-6-methoxy-3-(3,4,5-trimethoxybenzoyl)-benzo[b]furan 
• 945771-78-8 2-cyano-7-hydroxy-6-methoxy-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan 
• 905752-35-4 3-(3,4,5-trimethoxybenzoyl)-6-methoxy-7-isopropoxybenzo[b]furan 
• 1319803-92-3 7-isopropoxy-2-(3-isopropoxy-4-methoxyphenyl)-6-methoxy-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan 
• 945772-41-8 6-methoxy-2-methyl-7-(propan-2-yloxy)-3-(3,4,5-trimethoxybenzoyl)-1-benzofuran 
• 945772-45-2 C₂₀H₂₁O₁₀P 

Relevant academic research and scientific papers

A synthetic BNC105 method

The invention relates to a method for compounding BNC 105, which uses o-vanillin and 3,4,5- trimethoxy-benzaldehyde as starting materials. The o-vanillin is subjected to hydroxy protection and aldehyde oxidation to be hydrolyzed into phenol, and the pheno

CHEMICAL PROCESSES FOR THE MANUFACTURE OF SUBSTITUTED BENZOFURANS

The present invention relates to the scaled-up synthesis of biologically active compounds which display useful therapeutic activity in treating proliferative disorders. In particular the invention relates to process methods for the kilogram scale synthesi

An efficient synthesis and substitution of 3-aroyl-2-bromobenzo[b]furans

(Chemical Equation Presented) A convenient method for the synthesis of 2-bromo-3-aroyl-benzo[b]furans from readily accessible precursors has been developed. The 2-bromo group has been employed as a versatile synthetic handle in both palladium-mediated cou