210165-65-4 Usage
Molecular structure
bicyclic ring system with a nitrogen atom.
Substituents
two benzylamino groups at the 6α and 6β positions.
Compound class
azabicyclic compounds.
Potential applications
medicinal chemistry and drug development.
Utility
synthesis of pharmaceuticals or as a research tool in studying chemical and biological processes.
Further investigation
specific properties and potential uses need to be studied.
Check Digit Verification of cas no
The CAS Registry Mumber 210165-65-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,1,6 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 210165-65:
(8*2)+(7*1)+(6*0)+(5*1)+(4*6)+(3*5)+(2*6)+(1*5)=84
84 % 10 = 4
So 210165-65-4 is a valid CAS Registry Number.
210165-65-4Relevant articles and documents
Reductive decyanation of N-protected 6-amino-3-aza-bicyclo [3.1.0]hexanecarbonitriles
Vilsmaier, Elmar,Milch, Gunther,Bergstraesser, Uwe
, p. 6403 - 6414 (2007/10/03)
The cyano moiety in dibenzylamino-3-azabicyclo[3.1.0]hexane-6- carbonitriles 14c,d can be removed reductively by alkali metals: sodium in liquid ammonia at low temperatures causes a reaction with retention of configuration whilst lithium in an ethylamine - ammonia mixture at 0°C leads predominantly to inversion of configuration. The analogous diallylamino species 14e is less suitable for reductive decyanation. It can be used, however, for the synthesis of a 3-azabicyclo[3.2.0]heptane diamine 22. The solid state conformation of an N(3)-unsubstituted 3-azabicyclohexane skeleton is determined by an X-ray structural analysis.
