1432754-89-6

Basic information

• Product Name: 3,3-bis(4-((4,6-dimethoxy-1,3,5-triazin-2-yl)oxy)phenyl)isobenzofuran-1(3H)-one
• Synonyms: 3,3-bis(4-((4,6-dimethoxy-1,3,5-triazin-2-yl)oxy)phenyl)isobenzofuran-1(3H)-one
• CAS NO: 1432754-89-6
• Molecular Weight: 596.556
• Mol File: 1432754-89-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,3-bis(4-((4,6-dimethoxy-1,3,5-triazin-2-yl)oxy)phenyl)isobenzofuran-1(3H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3-bis(4-((4,6-dimethoxy-1,3,5-triazin-2-yl)oxy)phenyl)isobenzofuran-1(3H)-one(1432754-89-6)
• EPA Substance Registry System: 3,3-bis(4-((4,6-dimethoxy-1,3,5-triazin-2-yl)oxy)phenyl)isobenzofuran-1(3H)-one(1432754-89-6)

Safety Data

• Hazardous Substances Data: 1432754-89-6(Hazardous Substances Data)

Upstream product

• 3140-73-6 2-chloro-4,6-dimethoxy-1 ,3,5-triazine 
• 77-09-8 phenolphthalein 

Downstream Products

• 92688-34-1 3,3-di([1,1'-biphenyl]-4-yl)isobenzofuran-1(3H)-one 

Relevant articles and documents

Nickel-catalyzed Suzuki-Miyaura coupling of heteroaryl ethers with arylboronic acids

Nickel-catalyzed Suzuki-Miyaura coupling of heteroaryl ethers with arylboronic acids was described. Selective activation of the phenol C-O bonds was achieved by converting them into the corresponding aryl 2,4-dimethoxy-1,3,5- triazine-6-yl ethers, in which aryl C-O bond could be selectively cleaved with inexpensive, air-stable NiCl2(dppf) as a catalyst. Coupling of these readily accessible heteroaryl ethers proved tolerant of extensive functional groups.