168890-44-6 Usage
Description
2-(4-Fluoro-phenyl)-azepane, also known as fluoroazepane, is a chemical compound belonging to the azepane family, characterized by a seven-membered heterocyclic ring with a nitrogen atom and a fluorine atom attached to a phenyl group. With the molecular formula C13H15FN, fluoroazepane has potential applications in pharmaceuticals and drug development due to its possible biological activity and therapeutic properties.
Uses
Used in Pharmaceutical Industry:
2-(4-Fluoro-phenyl)-azepane is used as a chemical intermediate for the synthesis of various pharmaceutical compounds, leveraging its unique structure and potential biological activity to develop new drugs with therapeutic properties.
Used in Drug Development:
Fluoroazepane serves as a key component in drug development, where its specific molecular features may contribute to the creation of innovative medications with improved efficacy and selectivity in treating various diseases and conditions.
Research on the synthesis and properties of 2-(4-Fluoro-phenyl)-azepane is ongoing, aiming to further explore its potential uses and effects in the fields of pharmaceuticals and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 168890-44-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,8,9 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 168890-44:
(8*1)+(7*6)+(6*8)+(5*8)+(4*9)+(3*0)+(2*4)+(1*4)=186
186 % 10 = 6
So 168890-44-6 is a valid CAS Registry Number.
168890-44-6Relevant articles and documents
Synthesis of chiral cyclic amines via Ir-catalyzed enantioselective hydrogenation of cyclic imines
Zhang, Ying,Kong, Duanyang,Wang, Rui,Hou, Guohua
, p. 3006 - 3012 (2017)
A highly enantioselective hydrogenation of cyclic imines for synthesis of chiral cyclic amines has been realized. With the complex of iridium and (R,R)-f-spiroPhos as the catalyst, a range of cyclic 2-aryl imines were smoothly hydrogenated under mild conditions without any additive to provide the corresponding chiral cyclic amines with excellent enantioselectivities of up to 98% ee. Moreover, this method could be successfully applied to the synthesis of (+)-(6S,10bR)-McN-4612-Z.
