69971-90-0 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The core of the compound is a pyrrolidine ring, which is a five-membered ring containing four carbon atoms and one nitrogen atom.
Explanation
A naphthalene group is attached to the pyrrolidine ring, which is a fused pair of benzene rings.
Explanation
The compound has two carbonyl groups (C=O) attached to the pyrrolidine ring at the 2nd and 5th positions.
Explanation
It is a complex organic compound due to the presence of multiple functional groups and a fused ring system.
Explanation
The compound is used as a starting material for the synthesis of various other organic compounds.
Explanation
Due to its unique structure and properties, it may have potential applications in the development of new pharmaceuticals.
Explanation
Additional research and testing are required to fully understand the compound's potential uses and applications in various fields.
Central structure
Pyrrolidine ring
Attached group
Naphthalene
Functional groups
Two酮 (ketones) at positions 2 and 5
Type of compound
Complex organic compound
Usage
Building block in organic chemistry
Potential applications
Pharmaceutical industry
Further research
Necessary for exploring potential uses and applications
Check Digit Verification of cas no
The CAS Registry Mumber 69971-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,7 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69971-90:
(7*6)+(6*9)+(5*9)+(4*7)+(3*1)+(2*9)+(1*0)=190
190 % 10 = 0
So 69971-90-0 is a valid CAS Registry Number.
69971-90-0Relevant articles and documents
Nickel-Catalyzed Kumada Coupling of Boc-Activated Aromatic Amines via Nondirected Selective Aryl C-N Bond Cleavage
Zhang, Zheng-Bing,Ji, Chong-Lei,Yang, Ce,Chen, Jie,Hong, Xin,Xia, Ji-Bao
supporting information, p. 1226 - 1231 (2019/02/14)
A nickel-catalyzed Kumada coupling of aniline derivatives was developed by selective cleavage of aryl C-N bonds under mild reaction conditions. Without preinstallation of an ortho directing group on anilines, the cross-coupling reactions of Boc-protected aromatic amines with aryl Grignard reagents afforded unsymmetric biaryls. Mechanistic studies by DFT calculations revealed that the nickel-mediated C-N bond cleavage is the rate-limiting step.
