321569-83-9

Basic information

• Product Name: (E)-1-(2,4-Bis-benzyloxy-3-iodo-6-methoxymethoxy-phenyl)-3-(2,4-bis-benzyloxy-phenyl)-propenone
• CAS NO: 321569-83-9
• Molecular Weight: 818.705
• Mol File: 321569-83-9.mol

Chemical Properties

• CAS DataBase Reference: (E)-1-(2,4-Bis-benzyloxy-3-iodo-6-methoxymethoxy-phenyl)-3-(2,4-bis-benzyloxy-phenyl)-propenone(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-(2,4-Bis-benzyloxy-3-iodo-6-methoxymethoxy-phenyl)-3-(2,4-bis-benzyloxy-phenyl)-propenone(321569-83-9)
• EPA Substance Registry System: (E)-1-(2,4-Bis-benzyloxy-3-iodo-6-methoxymethoxy-phenyl)-3-(2,4-bis-benzyloxy-phenyl)-propenone(321569-83-9)

Safety Data

• Hazardous Substances Data: 321569-83-9(Hazardous Substances Data)

Upstream product

• 13246-46-3 2,4-dibenzyloxybenzaldehyde 
• 321569-81-7 2',4'-bis(benzyloxy)-3'-iodo-6'-(methoxymethoxy)acetophenone 
• 321569-79-3 2',4'-dihydroxy-3'-iodo-6'-(methoxymethoxy)acetophenone 

Downstream Products

• 321569-86-2 2,4,2',4'-tetrakis(benzyloxy)-6'-hydroxy-3'-iodochalcone 

Relevant articles and documents

Regioselective synthesis of prenylisoflavones: Syntheses of luteone and luteone hydrate

The palladium-catalyzed coupling reaction of 6-iodoisoflavone, prepared from 3′-iodoacetophenone derivative, with 2-methyl-3-butyn-2-ol gave the 6-alkynylisoflavone derivative, which was hydrogenaied to give the 6-alkylhydroxyisoflavone (luteone hydrate)