135159-04-5

Basic information

• Product Name: 8-[5-(5,7-Dimethoxy-4-oxo-4H-chromen-2-yl)-2-methoxy-phenyl]-5,7-diisopropoxy-2-(4-isopropoxy-phenyl)-chromen-4-one
• Synonyms: 8-[5-(5,7-Dimethoxy-4-oxo-4H-chromen-2-yl)-2-methoxy-phenyl]-5,7-diisopropoxy-2-(4-isopropoxy-phenyl)-chromen-4-one
• CAS NO: 135159-04-5
• Molecular Weight: 706.789
• Mol File: 135159-04-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 8-[5-(5,7-Dimethoxy-4-oxo-4H-chromen-2-yl)-2-methoxy-phenyl]-5,7-diisopropoxy-2-(4-isopropoxy-phenyl)-chromen-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 8-[5-(5,7-Dimethoxy-4-oxo-4H-chromen-2-yl)-2-methoxy-phenyl]-5,7-diisopropoxy-2-(4-isopropoxy-phenyl)-chromen-4-one(135159-04-5)
• EPA Substance Registry System: 8-[5-(5,7-Dimethoxy-4-oxo-4H-chromen-2-yl)-2-methoxy-phenyl]-5,7-diisopropoxy-2-(4-isopropoxy-phenyl)-chromen-4-one(135159-04-5)

Safety Data

• Hazardous Substances Data: 135159-04-5(Hazardous Substances Data)

Upstream product

• 3754-52-7 3'-iodo-5,7,4'-trimethoxyflavone 
• 135159-00-1 C₂₄H₂₉BO₇ 

Downstream Products

• 481-46-9 ginkgetin 

Relevant articles and documents

A new strategy for the synthesis of biflavonoids via arylboronic acids

Amentoflavone derivatives were prepared by catalytic coupling of 8-flavone-boronic acids with iodoflavones. 3-Arylflavones, as biflavonoid synthon, are accessible by the method.