111896-94-7 Usage
Bicyclic structure
azabicyclo[2.2.2]octane
The compound has a two-ring structure, with one of the rings being a seven-membered azabicycle (a nitrogen-containing ring) and the other a five-membered ring.
Derivative
benzodioxol-5-ylmethylidene
The compound is a derivative of azabicyclo[2.2.2]octane with a benzodioxol group attached to the structure.
Aromatic and ether-like properties
benzodioxol group
The presence of the benzodioxol group adds aromatic (ring-like) and ether-like (oxygen-containing) properties to the compound.
Potential applications
medicine and drug development
The compound may have potential uses in the fields of medicine and drug development due to its unique structure and properties.
Further research needed
properties and potential uses
More research is required to fully understand the properties and potential applications of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 111896-94-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,8,9 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 111896-94:
(8*1)+(7*1)+(6*1)+(5*8)+(4*9)+(3*6)+(2*9)+(1*4)=137
137 % 10 = 7
So 111896-94-7 is a valid CAS Registry Number.
111896-94-7Relevant articles and documents
Ruthenium-Catalyzed Highly Enantioselective Synthesis of cis-3-Quinuclidinols via DKR Asymmetric Transfer Hydrogenation
Luo, Zhonghua,Wang, Zhongqing,Sun, Guodong,Jian, Weilin,Jiang, Fengkai,Luan, Baolei,Li, Ridong,Zhang, Lei
supporting information, p. 4322 - 4326 (2020/06/04)
A method for the enantioselective synthesis of cis-3-quinuclidinols by Ru-catalyzed asymmetric transfer hydrogenation via dynamic kinetic resolution is described. The reaction proceeded under mild conditions using ammonium formate as the hydrogen donor, affording the products in high yields (up to 99%) with excellent diastereoselectivity (up to 99:1 dr) and enantioselectivity (95-99% ee). This protocol was applicable to gram-scale preparation with perfect enantioselectivity through simple recrystallization.