36896-62-5

Basic information

• Product Name: (2,4,6-trimethoxyphenyl)lead triacetate
• Synonyms: (2,4,6-trimethoxyphenyl)lead triacetate
• CAS NO: 36896-62-5
• Molecular Weight: 551.518
• Mol File: 36896-62-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2,4,6-trimethoxyphenyl)lead triacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (2,4,6-trimethoxyphenyl)lead triacetate(36896-62-5)
• EPA Substance Registry System: (2,4,6-trimethoxyphenyl)lead triacetate(36896-62-5)

Safety Data

• Hazardous Substances Data: 36896-62-5(Hazardous Substances Data)

Upstream product

• 621-23-8 1,2,3-trimethoxybenzene 
• 546-67-8 lead(IV) tetraacetate 

Downstream Products

• 124006-22-0 1,2,3,4-tetrahydro-2-(2,4,6-trimethoxyphenyl)isoquinoline 
• 124010-48-6 3-(2,4-dimethoxyphenyl)-4-hydroxy-5-methoxy-1-benzopyran-2-one 
• 124010-44-2 4-hydroxy-5-methoxy-3-(2,4,6-trimethoxyphenyl)-1-benzopyran-2-one 
• 1411858-79-1 3-allyl-3-(2,4,6-trimethoxyphenyl)chroman-4-one 
• 86564-22-9 7,2',4',6'-tetramethoxyisoflavone 
• 328314-32-5 6,7-dimethoxy-4-(2,4,6-trimethoxyphenyl)-2H-1-benzopyran-3(4H)-one 

Relevant articles and documents

Enantioselective construction of sterically hindered tertiary α-aryl ketones: A catalytic asymmetric synthesis of isoflavanones

A method for the catalytic asymmetric α-arylation of ketones bearing very sterically hindered aryl rings has been developed. This reaction occurs under mild conditions, in short reaction times and has been applied to the first catalytic asymmetric synthesis of isoflavanones.