95906-20-0

Basic information

• Product Name: 6-phenyl-4,4-tetramethylenespiro{(1,3-dioxa-4-azonia-2-boratacyclohexane)-2,1'-(4',5'-dihydrodibenzo{b,f}boratepin)}
• CAS NO: 95906-20-0
• Molecular Weight: 397.325
• Mol File: 95906-20-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 6-phenyl-4,4-tetramethylenespiro{(1,3-dioxa-4-azonia-2-boratacyclohexane)-2,1'-(4',5'-dihydrodibenzo{b,f}boratepin)}(CAS DataBase Reference)
• NIST Chemistry Reference: 6-phenyl-4,4-tetramethylenespiro{(1,3-dioxa-4-azonia-2-boratacyclohexane)-2,1'-(4',5'-dihydrodibenzo{b,f}boratepin)}(95906-20-0)
• EPA Substance Registry System: 6-phenyl-4,4-tetramethylenespiro{(1,3-dioxa-4-azonia-2-boratacyclohexane)-2,1'-(4',5'-dihydrodibenzo{b,f}boratepin)}(95906-20-0)

Safety Data

• Hazardous Substances Data: 95906-20-0(Hazardous Substances Data)

Upstream product

• 95906-19-7 C₆H₄CH₂CH₂C₆H₄BOCH₂CH₂NH₂ 
• 14746-43-1 N-(2-hydroxy-2-phenylethyl)pyrrolidine N-oxide 

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).