95890-61-2

Basic information

• Product Name: 2,2-di(1-naphthyl)-6-phenyl-4,4-tetramethylene-1,3-dioxa-4-azonia-2-boratacyclohexane
• CAS NO: 95890-61-2
• Molecular Weight: 471.407
• Mol File: 95890-61-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,2-di(1-naphthyl)-6-phenyl-4,4-tetramethylene-1,3-dioxa-4-azonia-2-boratacyclohexane(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-di(1-naphthyl)-6-phenyl-4,4-tetramethylene-1,3-dioxa-4-azonia-2-boratacyclohexane(95890-61-2)
• EPA Substance Registry System: 2,2-di(1-naphthyl)-6-phenyl-4,4-tetramethylene-1,3-dioxa-4-azonia-2-boratacyclohexane(95890-61-2)

Safety Data

• Hazardous Substances Data: 95890-61-2(Hazardous Substances Data)

Upstream product

• 6962-88-5 B-(2-aminoethoxy)di(1-naphthyl)borane 
• 14746-43-1 N-(2-hydroxy-2-phenylethyl)pyrrolidine N-oxide 

Downstream Products

• 95890-70-3 2-(1-naphthyloxy)-2-(1-naphthyl)-5-phenyl-3,3-tetramethylen-1-oxa-3-azonia-2-boratacyclopentane 

Relevant articles and documents

SYNTHESE UND THERMISCH INDUZIERTE UMLAGERUNG DER DIARYLBORCHELATE VON N-(2-HYDROXYALKYL)-N,N-DIALKYLAMIN-N-OXIDEN

Various diarylboron chelates of the cyclic B,N-betaine type (2,7,11) are synthesized from N-(2-hydroxyalkyl)-N,N-dialkylamine-N-oxides (1) and diarylboron reagents.They are rearranged in a thermally induced intramolecular redox reaction, during which the N-oxide is deoxygenated and the borinic acid moiety is oxidized to the state of boronic acid.The rearrangement products 3, 8 and 12 are converted to new B,N-betaine type chelates 5 and 9 by re-chelation with N-oxides (1).