15831-61-5

Basic information

• Product Name: Ethanol, 2-[oxidobis(phenylmethyl)amino]-
• CAS NO: 15831-61-5
• Molecular Formula: C16H19NO2
• Molecular Weight: 257.332
• Mol File: 15831-61-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Ethanol, 2-[oxidobis(phenylmethyl)amino]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanol, 2-[oxidobis(phenylmethyl)amino]-(15831-61-5)
• EPA Substance Registry System: Ethanol, 2-[oxidobis(phenylmethyl)amino]-(15831-61-5)

Safety Data

• Hazardous Substances Data: 15831-61-5(Hazardous Substances Data)

Upstream product

• 101-06-4 N,N-dibenzyl-2-aminoethanol 

Downstream Products

• 95890-34-9 4,4-dibenzyl-2,2-diphenyl-1,3-dioxa-4-azonia-2-boratacyclohexane 
• 95890-44-1 4,4-dibenzyl-2,2-bis(4-methoxyphenyl)-1,3-dioxa-4-azonia-2-boratacyclohexane 
• 95890-58-7 4,4-dibenzyl-2,2-di(1-naphthyl)-1,3-dioxa-4-azonia-2-boratacyclohexane 
• 95890-51-0 4,4-dibenzyl-2,2-bis(4-chlorophenyl)-1,3-dioxa-4-azonia-2-boratacyclohexane 

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).